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Walgreens
Updated: September 22, 2020 12:00 PM
Covid-19 OSHA Complaint, Walgreens, 2420 N Blackstone Ave, Fresno, California 93703, USA
Walgreens, 2420 N Blackstone Ave, Fresno, California 93703, USA
September 22, 2020 12:00 PM
“GISO: CCR Title-8 5199
1. Employer is not taking employee temperatures of employees.
2. Employer is not enforcing the wearing of facemasks.
Alleged Hazards: 2, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-07-17 See Less”
Helpful
Covid-19 OSHA Complaint, Walgreens, Alameda, California 94501, USA
Walgreens, Alameda, California 94501, USA
September 22, 2020 12:00 PM
“1. The employer does not enforce the use of face coverings over mouth and nose by cash register employees. T8 CCR 3203(a)(4) & (6)
Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-08-25 See Less”
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Covid-19 OSHA Complaint, Walgreens, Guaynabo, 00966, Puerto Rico
Walgreens, Guaynabo, 00966, Puerto Rico
September 17, 2020 12:00 PM
“1.Patron did not follow an Exposure Control Plan to COVID-19 when an employee was positive for the virus.
2. They don't have a continuous cleaning protocol.
3. They do not control the number of people in the property.
Alleged Hazards: 3, Employees Exposed: 50
Source: OSHA.gov | Receipt D... See Moreate: 2020-07-29 See Less”
Helpful
Covid-19 OSHA Complaint, Walgreens, 12335 NE Glisan St, Portland, Oregon 97230, USA
Walgreens, 12335 NE Glisan St, Portland, Oregon 97230, USA
September 17, 2020 12:00 PM
“Serious
Alleged Hazards: 1,
Source: Osha.gov | Receipt Date: 2020-07-20 See Less”
Helpful
Unknown number of employees test positive for Covid-19, Walgreens, 1096 South Saint Francis Drive, Santa Fe, NM, USA
Walgreens, 1096 South Saint Francis Drive, Santa Fe, NM, USA
September 10, 2020 12:00 PM
“Unknown number of employees at WALGREENS in SANTA FE, NM tested positive for Covid-19. Event Date: 09/10/2020
Source: env.nm.gov See Less”
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An employee test positive for Covid-19, Walgreens, 700 E 21st St, Clovis, NM, USA
Walgreens, 700 E 21st St, Clovis, NM, USA
September 7, 2020 12:00 PM
“An employee(1) at Walgreens in Clovis, NM tested positive for Covid-19. Event Date: 09/05/2020
Source: env.nm.gov See Less”
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Covid-19 OSHA Complaint, Walgreens, 1585 Randolph Ave, Saint Paul, Minnesota 55105, USA
Walgreens, 1585 Randolph Ave, Saint Paul, Minnesota 55105, USA
September 7, 2020 12:00 PM
“The following step is not adequately taken to prevent the spread of COVID-19 in the workplace and protect employees working in the area:
1. Employees are permitted to work without wearing the face coverings required by the MN Executive Order. Note: face coverings must cover mouth and nose not ju... See Morest mouth.
2. Customers are allowed in the store without a face covering, putting employees at risk.
Source: Osha.gov | Receipt Date: 2020-08-12 See Less”
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Covid-19 OSHA Complaint, Walgreens, 2788 River Rd, Eugene, Oregon 97404, USA
Walgreens, 2788 River Rd, Eugene, Oregon 97404, USA
September 7, 2020 12:00 PM
“Serious
Alleged Hazards: 1,
Source: Osha.gov | Receipt Date: 2020-07-22 See Less”
Helpful
Covid-19 OSHA Complaint, Walgreens, 2300 Otis Drive, Alameda, California 94501, USA
Walgreens, 2300 Otis Drive, Alameda, California 94501, USA
September 7, 2020 12:00 PM
“The employer is not cleaning and sanitizing restrooms. Internal guidance that the restrooms be cleaned at least twice a week is not being followed and implemented. Non-janitorial employees are asked to clean the restroom without proper training, are not provided sufficient time to thoroughly clean t... See Morehe restrooms, and are told not to sanitize toilets. T8 CCR 3203(a)(4), (6) &(7) and 3364(b)
Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-07-20 See Less”
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An employee test positive for Covid-19, Walgreens, 1225 North Turner Street, Hobbs, NM, USA
Walgreens, 1225 North Turner Street, Hobbs, NM, USA
August 30, 2020 12:00 PM
“An employee(1) at Walgreens in Hobbs, NM tested positive for Covid-19. Event Date: 08/28/2020
Source: env.nm.gov See Less”
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Recent Interesting Reports
September 7, 2020 8:36 PM
“The CFIA announced the recall of Frank brand Milk Chocolate Covered Raisins by Canadian Tire Corporation of Canada from the marketplace due to undeclared peanut.
- Frank Milk Chocolate Covered Raisins (300 g). UPC: 6 26394 33920 7. Best Before 2021 MA 07, Lot: 07EUA | Best Before 2021 MA 13, Lot... See More: 13EUA | Best Before 2021 JL 07, Lot: 07GUB | Best Before 2021 APR 21, Lot: 21DUB | Best Before 2021 JL 08, Lot: 08GUB
Check the full recall details on the CFIA website: inspection.gc.ca
Source: CFIA See Less”
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September 20, 2020 9:38 PM
“The CFIA announced the recall of PC Blue Menu brand Artichoke & Asiago Dip by Loblaw Companies Limited from the marketplace due it may contain egg which is not declared on the label. There have been no reported illnesses associated with the consumption of this product.
CFIA advises consumers not... See Moreto eat the recalled products and return them to the place of purchase for a full refund. The products were distributed nationwide.
- PC Blue Menu Artichoke & Asiago Dip (on lid) (side label states Tzatziki Yogurt Dip). Size: 227 g. UPC: 0 60383 03697 3. Codes: 2020 OC 31.
Check the full recall details on the CFIA website inspection.gc.ca
Source: CFIA See Less”
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Long black curly hair wrapped into my cheeseburger, McDonald's, 1219 Marine Dr, North Vancouver, BC V7P 1T3, Canada
McDonald's, 1219 Marine Dr, North Vancouver, BC V7P 1T3, Canada
September 14, 2020 10:41 AM
“I was do discussed I took one bite of my cheeseburger There was a long black curly hair wrapped into all around the burger it wasn't just a little piece of hair it was long and curly very bad turned me off from eating there now and I ate there lots it was on 09/05/2020 @ 2:46pm I took it back to the... See Morem rite away. I haven't posted the picture .. yet but feel like I should People shouldn't have to check and look at ther food especially from a place like this should n able to trust that ther nothing in there that shouldn't b why are they not wearing hair nets!? I watched the girls making the food in the back no one is wearing hair nets See Less”
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Ready-To-Eat Chicken Salad Products -recalled due to Misbranding and an Undeclared Allergen, USA
USA
September 16, 2020 9:38 PM
“The FSIS announced the recall of approximately 6,890 pounds of ready-to-eat (RTE) chicken salad products by Willow Tree Poultry Farm, Inc due to misbranding and an undeclared allergen. The products may contain walnuts, a known allergen, which are not declared on the product labels. There have been n... See Moreo confirmed reports of adverse reactions due to consumption of these products to date.
FSIS advises consumers not to eat the recalled products and to throw them away or return them to the place of purchase. The RTE chicken salad product labeled as “Classic Chicken Salad” may actually contain “White Meat Cranberry Walnut Chicken Salad” and was produced on Sept. 2, 2020. The products subject to recall bear establishment number “EST. P-8827” inside the USDA mark of inspection. These items were shipped to retail locations in Connecticut, the District of Columbia, Maine, Maryland, Massachusetts, New Hampshire, Rhode Island, Vermont and Virginia. The following products are subject to recall:
- 15-oz. clear, plastic containers labeled as “Willow Tree Premium White Meat CHICKEN SALAD Classic” with a sell by date of “9/30/20” and a time stamp of 13:00:00 through 17:00:00 on the containers’ cellophane lid.
Check the full recall details on the FSIS website fsis.usda.gov
Source: FSIS See Less”
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September 11, 2020 4:00 PM
“Company name: Goodie Girl Tribeca LLC
Brand name: Goodie Girl
Product recalled: Goodie Girl GF Magical Animal Crackers
Reason of the recall: May Contain Undeclared Wheat
FDA Recall date: September 11, 2020
Recall details: Goodie Girl Tribeca LLC announced today it is voluntarily recalling 389... See Morecases of a single date code of 7 oz. Goodie Girl Magical Animal Crackers, with a “best by” date of Jan 11, 21A3, after learning that the product may contain undeclared wheat ingredients. People who have an allergy or severe sensitivity to wheat run the risk of allergic reaction if they consume the product contained in the recalled boxes. There has been an individual with a wheat allergy that was treated for a wheat allergen reaction.
This recall affects only 389 cases of the following product, which were distributed in retail stores nationwide:
- Description; Goodie Girl GF Magical Animal Crackers
UPC# 8-5598700395-3
Size; 7 Ounces
Best By Date; Jan 11, 2021
Distributed between 4/17/2020 – 5/7/2020
This recall does not apply to any other “best by” dates, sizes or varieties of Goodie Girl Tribeca LLC. This recall was initiated in cooperation with the FDA and the third-party co-packer that produced the product. Product with this particular “best by” date was shipped and distributed by Goodie Girl Tribeca to its customers' warehouses located in Virginia, Pennsylvania, Georgia, New Hampshire, California. Consumers seeking a refund or additional information may contact info@goodiegirl.com or call 201-941-2000 9am – 5pm est.
Check the full recall details on fda.gov
Source: FDA See Less”
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Pretty Thai Sweat Chili Sauce - recalled due to May contain Pretty Thai Peanut Sauce, Paint Rock, TX, USA
Paint Rock, TX, USA
September 10, 2020 9:00 PM
“Company name: Pretty Thai
Brand name: Pretty Thai
Product recalled: Pretty Thai Sweat Chili Sauce
Reason of the recall: May contain Pretty Thai Peanut Sauce
FDA Recall date: September 10, 2020
Recall details: Company Announcement Pretty Thai of Austin, Texas, is recalling Pretty Thai Peanut Sau... See Morece that may have been mislabeled as Pretty Thai Sweet Chili Sauce. There is a risk that a person with an allergy or severe sensitivity to peanuts could unintentionally consume a product containing peanuts because of this error. No illnesses have been reported to date.
The product was distributed to H-E-B and Central Market stores in Texas from March 19, 2020 to September 8, 2020. The product is packaged in clear, cylindrical PET bottles with black flip-top caps and clear labels with white print. The recall is for Pretty Thai Peanut Sauce with the Lot Code 0772000123. A small number of the Pretty Thai Peanut Sauce bottles were discovered to have been mislabeled as Pretty Thai Sweet Chili Sauce. Pretty Thai Peanut Sauce is yellow or gold in color, while Pretty Thai Sweet Chili Sauce is dark red in color. People who have an allergy or severe sensitivity to peanuts run the risk of serious or life-threatening allergic reaction if they consume the mislabeled product.
Pretty Thai and its manufacturer, Ponder Foods, have coordinated efforts with H-E-B to remove all of the affected product from the shelves and from distribution. Out of an abundance of caution, we are alerting consumers in Texas who may have purchased either Pretty Thai Peanut Sauce or Pretty Thai Sweet Chili Sauce to check any product for Lot Code 0772000123. For consumers with no peanut allergy, this Lot Code of Pretty Thai Peanut Sauce, as well as any Lot Code of Pretty Thai Sweet Chili Sauce are completely safe to consume. Product may be returned to H-E-B and/or Central Market for a full refund. Subsequent investigation indicates the problem was caused by a temporary breakdown in the manufacturer's production and packaging processes.
Consumers with questions may contact the Pretty Thai brand directly via email at info@ptfawg.com or via telephone at 512 981 6170. Consumers or retailers may also contact the manufacturer, Ponder Foods, via email at info@ponder-foods.com or via telephone at 469 914 0052 (M-F, 9:00am-5:00pm CDT). Attached below is a photo of the mislabeled product with the affected Lot Code.
Check the full recall details on fda.gov
Source: FDA See Less”
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August 31, 2020 4:00 PM
“Company name: Mylan N.V.
Brand name: Mylan
Product recalled: Tranexamic Acid and Amiodarone HCl injections
Reason of the recall: Vials potentially packaged in incorrect cartons
FDA Recall date: August 31, 2020
Recall details: Mylan N.V. (NASDAQ: MYL) today announced that its U.S.-based Mylan In... See Morestitutional LLC business is conducting a voluntary nationwide recall to the hospital/clinic level of four lots of Amiodarone HCl Injection, USP 450 mg/9 mL, packaged in cartons of 10 single-dose 9 mL vials and Tranexamic Acid Injection, USP 1000 mg/10 mL, packaged in cartons of 10 single-dose 10 mL vials.
These batches are being recalled due to the potential for cartons labeled as Tranexamic Acid Injection, USP to contain vials of Amiodarone HCl Injection, USP and cartons labeled as Amiodarone HCl Injection, USP to contain vials of Tranexamic Acid Injection, USP. The individual vials contained within the cartons are accurately labeled as Amiodarone HCl Injection, USP or Tranexamic Acid Injection, USP. Both of these medications are administered in a hospital setting only by trained healthcare professionals. To date, Mylan has not received any reports of adverse events related to this recall.
Amiodarone HCl Injection, USP and Tranexamic Acid Injection, USP are used to treat different conditions. If Tranexamic acid is administered to a patient in place of Amiodarone or vice versa, it could present a risk to patient safety. If Amiodarone HCl Injection is inadvertently administered it could result in low blood pressure and irregular heartbeat, including lower than expected heart rate, which could have immediate life-threatening effects on cardiac function. If treatment with Amiodarone HCl Injection, when needed, is delayed this could result in continued irregular heartbeat and potential life-threatening effects on cardiac function.
If Tranexamic Acid Injection is inadvertently administered it could result in adverse events, including blood clotting, seizures, hypersensitivity reactions, visual disturbances, and dizziness. If treatment with Tranexamic Acid Injection, when needed, is delayed this could result in limited to serious and life-threatening bleeding events. Amiodarone HCl Injection, USP is an antiarrhythmic agent indicated for initiation of treatment and prophylaxis of frequently recurring ventricular fibrillation (VF) and hemodynamically unstable ventricular tachycardia (VT) in patients’ refractory to other therapy. Tranexamic acid injection is indicated in patients with hemophilia for short term use to reduce or prevent hemorrhage and reduce the need for replacement therapy during and following tooth extraction.
These batches were distributed nationwide in the USA to wholesalers and hospital/clinical pharmacies between April 2020 and July 2020. The recalled batch information is as follows:
NDC #: 67457-153-09
Material Description: Amiodarone HCl Injection, USP
Strength: 450 mg/9 mL
Carton Size: 10 x 9 mL single-dose vials
Lot No.: 191207 / 191221 / 191223 / 200120
Expiry: Nov. 2021 / Nov. 2021 / Nov. 2021 / Nov. 2021
NDC #: 67457-197-10
Material Description: Tranexamic Acid Injection, USP
Strength: 1000 mg/10 mL
Carton Size: 10 x 10 mL single-dose vials
Lot No.: 191207 / 191221 / 191223 / 200120
Expiry: Nov. 2021 / Nov. 2021 / Nov. 2021 / Nov. 2021
Mylan is notifying its wholesalers and hospital/clinic pharmacies by letter and is arranging for return of recalled products to Stericycle. Wholesalers and hospital/clinic pharmacies that have product which is being recalled should stop use/further distribution or dispensing.
Check the full recall details on fda.gov
Source: FDA See Less”
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September 17, 2020 11:00 PM
“Company name: Acella Pharmaceuticals, LLC
Brand name: NP Thyroid 15 & NP Thyroid120
Product recalled: Thyroid Tablets
Reason of the recall: Sub Potency
FDA Recall date: September 17, 2020
Recall details: Acella Pharmaceuticals, LLC is voluntarily recalling one lot of 15-mg and one lot of 120-mg... See MoreNP Thyroid®, Thyroid Tablets, USP [levothyroxine (T4) and liothyronine (T3)] to the consumer level. The products are being recalled because testing has found these lots to be sub potent. The product may have as low as 87% of the labeled amount of levothyroxine (T4). More information can be found at www.npthyroid.com/product-updates.
Risk Statement: Patients being treated for hypothyroidism (underactive thyroid), who receive sub potent NP Thyroid®, may experience signs and symptoms of hypothyroidism (underactive thyroid) which may include, fatigue, increased sensitivity to cold, constipation, dry skin, puffy face, hair loss, slow heart rate, depression, swelling of the thyroid gland and/or unexplained weight gain or difficulty losing weight. There is reasonable risk of serious injury in newborn infants or pregnant women with hypothyroidism including early miscarriage, fetal hyperthyroidism, and/or impairments to fetal neural and skeletal development. In elderly patients and patients with underlying cardiac disease toxic cardiac manifestations of hyperthyroidism may occur, such as cardiac pain, palpitations or cardiac arrhythmia.
To date, Acella has received four reports of adverse events for these lot numbers possibly related to this recall. NP Thyroid®, Thyroid Tablets, USP is composed of levothyroxine and liothyronine, and used to treat hypothyroidism (underactive thyroid). The products subject to recall are packed in 100-count bottles. See product images. To best identify the product, the NDC’s, Product Description, Lot Numbers and Expiration Dates are listed. These lots were distributed nationwide in the USA to Acella’s direct accounts, including wholesalers, pharmacies, and healthcare offices. Additionally, consumers may be able to determine that their product is not impacted by the recall if the “use by,” “discard after,” or “expiration date” on their prescription bottle is on or after December 2020.
Product NDC Lot # Exp. Date
NP Thyroid® 15, Thyroid Tablets, USP, ¼ grain (15 mg) 42192-327-01 M327E19-1 October 2020
NP Thyroid® 120, Thyroid Tablets, USP, 2 grain (120 mg) 42192-328-01 M328F19-3 November 2020
Acella is proactively notifying its wholesalers by email and phone to discontinue distribution of the two above referenced lots being recalled and is arranging for return of all recalled products. Patients who are currently taking NP Thyroid® from the lots being recalled should not discontinue use without contacting their healthcare provider for further guidance and/or a replacement prescription.
Check the full recall details on fda.gov
Source: FDA See Less”
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September 1, 2020 4:38 PM
“The FSIS announced the recall of approximately 1,202 pounds of ready-to-eat (RTE) chicken salad product by Ukrop’s Homestyle Foods due to misbranding and an undeclared allergen. The product may contain almonds, a known allergen, which are not declared on the product label.
The RTE chicken salad i... See Moretem was produced on August 26, 2020. The following product is subject to recall:
- 15-oz. round plastic containers containing “Ukrop’s Chicken Salad” with a sell by date of “09/02/20”.
The product subject to recall bears establishment number “P-19979” inside the USDA mark of inspection. These items were shipped to retail locations in North Carolina, Ohio, Virginia, and West Virginia. The problem was discovered after the firm received a consumer complaint reporting that the product contained almonds.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.
FSIS is concerned that some product may be in retailer and consumers’ refrigerators. Retailers who have obtained these products are urged not to sell them. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify that recalling firms are notifying their customers of the recall and that actions are being taken to make certain that the product is no longer available to consumers. Consumers and members of the media with questions about the recall can contact Susan Rowe, Executive Administrator, Ukrop’s Homestyle Foods, at (804) 340-3050.
Check the full recall details on the FSIS website fsis.usda.gov
Source: FSIS See Less”
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bio aaa Hand Sanitizer - recalled due to Possible presence of methanol, Miami, FL, USA
Miami, FL, USA
September 3, 2020 7:00 PM
“Company name: AJR Trading LLC
Brand name: bio aaa
Product recalled: Hand Sanitizer
Reason of the recall: Possible presence of methanol
FDA Recall date: September 03, 2020
Recall details: AJR Trading is voluntarily recalling 2,004 units of lot 20DF8307 of bio aaa Advance Hand Sanitizer currentl... See Morey in US distribution, packaged in 480 mL bottles, to the consumer level. This lot of bio aaa Advance Hand Sanitizer has been tested and meets all appropriate specifications and tests. However, in an abundance of caution, these units are being recalled because of possible presence of methanol in other lots of bio aaa Advance Hand Sanitizer.
Risk Statement: Substantial methanol exposure could result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma, permanent damage to the nervous system, or death. Although all persons using these products on their hands may be at risk; young children who accidently ingest them and adolescents and adults who drink these products as an alcohol (ethanol) substitute, are most at risk for methanol poisoning.
To date, AJR Trading has not received reports of adverse events related to this recall.
The product is used as a hand sanitizer to reduce bacteria when soap and water is not available and is packaged in 480 mL plastic bottles UPC 7502272121085. AJR Trading is recalling lot 20DF8307, expiration date April 2022. The product can be identified by the images below. Product was distributed in Miami beginning in April 2020. AJR Trading is notifying its customers by phone calls, e-mails, and letters. AJR Trading is arranging for refund and destruction of recalled products.
Consumers/distributors/retailers that have the above listed lots of bio aaa Hand Sanitizer, which is being recalled, should stop using or distributing the products immediately and mail the products to AJR Trading at the following address for refund: 814 Ponce de Leon Blvd, suite 218. Coral Gables, FL. 33134. Consumers with questions regarding this recall can contact AJR Trading by phone insert 305-302-8416 or e-mail to ajrtrading15@gmaill.com Monday to Friday from 10:00 am to 5:00 pm Central Time.
Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product. Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax. Complete and submit the report Online
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
Check the full recall details on fda.gov
Source: FDA See Less”
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