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Home Chef Cali Branch Office, 1445 S Tippecanoe Ave, San Bernardino, CA 92408, USA

Latest report: January 15, 2022 5:52 PM
#drugs #foodsafetyissue #osha #1445southtippecanoeavenue #sanbernardino #california #unitedstates
LH

Home Chef - Employee doing drugs at work on the job

4 months ago

The employee that is working for your company is doing drugs and other things I can't tell what the other things are because I don't know what they are right now but they need to be let go this job is what is a big part of... See More him getting the drugs I just don't know how he is doing it but when I do find out how it is being done I will be reporting it too for the safely of others please drug test the employee and watch them and theiir actions when on the job . See Less
1.4K


VR

Covid-19 OSHA Complaint

9 months ago

T8CCR 3205(c)(6)(A) Employer not staggering lunch and break times to ensure that employees are able to be separated from other persons by at least six feet.

Alleged Hazards: 1, Employees Exposed: 13
Source: Osha.gov | Receipt Date: 2021-04-19 See Less
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St. Paul, Minnesota, Fagron Inc. (“Fagron”) is voluntarily recalling two lots of SyrSpend SF Cherry to the hospital, pharmacy, and distributor level out of an abundance of caution. The affected lots are potentially contaminated with Burkholderia gladioli.

Burkholderia gladioli is an opportunistic pathogen most commonly affecting patients... See More with respiratory disease. Patients with compromised immune systems such as those with Cystic Fibrosis are at higher risk. Burkholderia gladioli also can cause complications after transplants. Exposure to contaminated product could lead to adverse events, which could be severe for at-risk individuals.

Fagron has received three complaints regarding an undesirable smell associated with the product. To date, Fagron has not received any reports of adverse events related to the product being recalled. Fagron sells this product for the extemporaneous compounding of prescriptions for oral dosing. The affected lots with expiration dates are listed below.

Affected products:
Lot: A67185
Item number: 805359
Size: 500 mL
NDC number: 51552-1123-5
Expiration date: 08/31/2024

Lot: A67186
Item number: 802496
Size: 4 L
NDC number:51551-1123-9
Expiration date: 08/31/2024

Fagron has already notified its distributors and customers by phone, e-mail, and/or letter and is arranging for return of all recalled products. Hospitals, pharmacies, and distributors that possess affected product should quarantine this material and await further instructions from Fagron or Fagron’s recall coordinator. Please immediately discontinue use or distribution of the recalled product. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this product.

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

Company name: Fagron Inc.
Brand name: Fagron
Product recalled: SyrSpend SF 500mL and 4L
Reason of the recall: Potential contamination with Burkholderia gladioli
FDA Recall date: May 02, 2022

Source: fda.gov
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Teva Pharmaceuticals USA has initiated a voluntary nationwide recall of a single lot of Anagrelide Capsules, USP 0.5 mg (Lot number GD01090), to the consumer level in the United States. This voluntary recall was initiated due to dissolution test failure detected during routine stability testing. No other... See More lots are impacted.

The recalled product is:
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NDC: 0172-5241-60
Lot # GD01090
Exp. Date 05/2022

Administration of this product with lower dissolution – taking longer to dissolve once ingested -- may result in decreased effectiveness or ineffectiveness of the drug to exert its platelet-reducing effect. Failed dissolution can result in a slower rate and extent of drug release leading to less anagrelide available in the body. For seriously ill patients with elevated platelet counts, less available anagrelide in the body could increase the risk of clotting (blood coagulation), and clotting or bleeding events such as a heart attack or stroke, which could be life-threatening. To date, Teva has not received any product quality complaints or adverse event reports, of this nature, for the recalled lot.

Anagrelide capsules are indicated for the treatment of patients with thrombocythemia, secondary to myeloproliferative neoplasms, to reduce the elevated platelet count and the risk of thrombosis and to ameliorate associated symptoms including thrombo-hemorrhagic events. Information about the affected lot is listed in the table below. It is packed in bottles with 100 Capsules. Teva distributed 4224 bottles nationwide from 07-30-2020 through 09-02-2020 to its wholesale, distributor and retail customers under the label for Teva Pharmaceuticals USA, Inc.

Company name: Teva Pharmaceuticals USA
Brand name: Teva
Product recalled: Anagrelide Capsules
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FDA Recall date: May 23, 2022

Source: fda.gov
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T8CCR 3205(c)(8)(C) Custodial employees do not sanitize areas where Covid-19 people had been in the classrooms and other areas, exposing teachers and other employees to Covid-19. T8CCR 3205(c)(8)(C) T8CCR 3203(a)(7) Custodial employees have not been trained to sanitize surfaces after someone had been declared sick with Covid-19.... See More T8CCR 3205(c)(8)(C) T8CCR 3203(a)(7) Custodial employees have not been trained on the proper use, and hazards of sanitation products to help with reduction of Covid-19 spread.

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Natural Organics, Inc., is voluntarily recalling four lots of NaturesPlus Keto Living Sugar Control Capsules 90 count, because it was found to contain gluten. People who have allergies to wheat or gluten run the risk of serious or life-threatening allergic reactions if they consume these products. There... See More have been no reported incidents of illness or adverse reactions in connection with these products to date.

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- NATURES PLUS KETO LIVING SUGAR CONTROL CAPSULES, 90 CAPSULES, Product No. 82004, UPC Code 097467820043, Lots 1362073, Best By 10/2025 and 1365200, Best By 10/2025
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Consumers who may have purchased affected lots of NaturesPlus Keto Living Sugar Control Capsules are advised to return them to the place of purchase. No other Natural Organics, Inc. products are affected by this recall. Natural Organics, Inc. has removed all affected products within existing inventory.

This voluntary recall is announced in accord with FDA guidelines. We are initiating recall notices to our accounts and consumers who received inventory of the recalled products with instructions for returning the recalled products and for notifying their customers of the recall. Consumers with questions may contact the company Monday – Friday, from 8:00 am to 4:30pm EDT.

Company name: NATURAL ORGANICS, INC
Brand name: NaturesPlus
Product recalled: Keto Living Sugar Control Capsules
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FDA Recall date: May 06, 2022

Source: fda.gov
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