Thank you for your report!
IMPORTANT - YOUR REPORT IS QUEUED - IT MAY TAKE UP TO 12 HOURS FOR YOUR REPORT TO SHOW ON OUR HOME PAGE (IF NOT OPTED AS PRIVATE)
Goodbye! and best wishes in your recovery
Recent Interesting Reports
Nipomo, CA, USA
May 4, 2021 11:48 PM
“I was sent a comando chain instead this company is a fraud and PayPal let it happen 😡😡😡🤦🏽♀️🤬 ”
May 13, 2021 2:01 PM
“Company name: Global Sanitizers
Brand name: Medically Minded
Product recalled: Hand Sanitizer
Reason of the recall: Presence of methanol
FDA Recall date: May 13, 2021
Recall details: Las Vegas, NV, Global Sanitizers is voluntarily recalling 50 thousand units of Medically Minded hand sanitizers,... lot numbers: E212020 & E082020 Best Buy of 5/21/2022 to the user/consumer level. FDA analysis has found the product to contain methanol.
Risk Statement: Substantial methanol exposure can result in coma, seizures, permanent blindness, permanent damage to the central nervous system, or death. Although all persons using these products on their hands are at risk, young children who accidently ingest these products and adolescents and adults who drink these products as an alcohol (ethanol) substitute, are most at risk for methanol poisoning.
To date, Global Sanitizers has not received any reports of adverse events related to this recall. These products are used as hand sanitizers and marketed to help decrease bacteria on the skin when soap and water are not available. Medically Minded hand sanitizer is packaged in 8.5 oz / 250 ml clear bottles with caps with the following UPC 7675300359. The affected Medically Minded hand sanitizer lots include the following lot numbers and expiration dates E212020 & E082020 Best Buy of 5/21/2022. The product can be identified by the representative label below.
The hand sanitizer was distributed Nationwide in the USA to Wholesale companies who further distributed between July 2020 -August 2020. Global Sanitizers is notifying its distributors and customers by Email, Letter, Telephone & Press Release and is arranging for return of all recalled products. Consumers/distributors/retailers that have Medically Minded hand sanitizer product which is being recalled should stop using/return to place of purchase/discard/contact their doctor.
Consumers with questions regarding this recall can contact Global Sanitizers by calling 702.323.4402 or e-mail address firstname.lastname@example.org Monday through Friday 9am-5pm pacific standard 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.
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 ”
Hospira 0.5% Bupivacaine Hydrochloride Injection and 1% Lidocaine HCl Injection - recalled due to mislabeling, USA
May 4, 2021 9:01 PM
“Company name: Hospira, Inc.
Brand name: Hospira, Inc.
Product recalled: 0.5% Bupivacaine Hydrochloride Injection, USP 30 mL and 1% Lidocaine HCl Injection, USP 30 mL
Reason of the recall: Due to mislabeling
FDA Recall date: May 04, 2021
Recall details: Hospira, Inc., a Pfizer company, is volun... tarily recalling lot EG6023 of 0.5% Bupivacaine Hydrochloride Injection, USP 30 mL and lot EG8933 of 1% Lidocaine HCl Injection, USP 30 mL, to the hospital/institution level due to mislabeling whereby a portion of each lot was incorrectly labeled as the other product. This issue was identified as part of the investigation of a confirmed customer report.
Hospira’s assessment of the potential risk to patients concluded that the use of the impacted product is likely to cause adverse events of moderate to high severity. If 1% lidocaine is administered to the patient instead of 0.5% bupivacaine, the patient may be underdosed, leading to lack of efficacy with potential outcomes such as inadequate pain management, and failure of surgical anesthesia. If 0.5% bupivacaine is administered to the patient instead of 1% lidocaine, an overdose of bupivacaine may occur, which could lead to potential outcomes such as seizures; respiratory abnormalities including low oxygen and/or elevated carbon dioxide in the blood, too much acid in the body fluids, and temporary cessation of breathing; heart abnormalities such as heart contraction and/or relaxation issues, irregular heartbeat, slower than normal heart rate, abnormal heart rhythm in which the ventricles of the heart quiver instead of pumping normally, cardiac arrest and cardiac flatline.
To date, Hospira, Inc. has not received reports of any adverse events associated with this issue for these lots. 0.5% Bupivacaine Hydrochloride Injection, USP is indicated in adults for the production of local or regional anesthesia or analgesia for surgery, dental and oral surgery procedures, diagnostic and therapeutic procedures, and obstetrical procedures. 1% Lidocaine HCl Injection, USP is indicated for the production of local or regional anesthesia by infiltration techniques such as percutaneous injection and intravenous regional anesthesia by peripheral nerve block techniques such as brachial plexus and intercostal and by central neural techniques such as lumbar and caudal epidural blocks when the accepted procedures for these techniques as described in standard textbooks are observed.
The NDC, Lot Number, Expiration Date, Strength and Configuration details for 0.5% Bupivacaine Hydrochloride Injection, USP and 1% Lidocaine HCl Injection, USP are in the table below and a photo of the products can be found at the end of this press release. The product lots were distributed nationwide to wholesalers, distributors, retailers, and hospitals in the United States, Puerto Rico and Guam from December 29, 2020 to April 15, 2021.
- 0.5% Bupivacaine Hydrochloride Injection, USP, Single Dose Teartop Vial. NDC: Vial: 0409-1162-19 Tray: 0409-1162-02. Lot number: EG6023. Expiration Date: 01 July 2022. Strength: 0.5%, 150 mg/30 mL (5 mg/mL). Configuration/ Count: Case Pack 2 x 25 Vials.
- 1% Lidocaine HCl Injection, USP Single Dose Teartop Vial. NDC: Vial: 0409-4279-16 Tray: 0409-4279-02. Lot number: EG8933. Expiration Date: 01 Aug 2022. Strength: 1%, 300 mg/30 mL (10 mg/mL). Configuration/ Count: Case Pack 2 x 25 Vials.
Hospira, Inc., places the utmost emphasis on patient safety and product quality at every step in the manufacturing and supply chain process. Hospira, Inc. has notified wholesalers, distributors, retailers, and hospitals by mail to arrange for return of any recalled product.
Wholesalers, distributors or retailers with an existing inventory of the lot, which is being recalled, should stop administration and distribution and quarantine immediately. If you have further distributed the recalled product, to the wholesale or retail level, please notify any accounts or additional locations which may have received the recalled product from you.
Hospitals/Institutions should inform Healthcare Professionals in your organization of this recall. For additional assistance, call Stericycle at 1-800-805-3093 between the hours of 8 a.m. to 5 p.m. ET, Monday through Friday.
Check the full recall details on fda.gov
Source: FDA ”
Symptoms: Fatigue Lightheaded Muscle Pain Soreness
Walgreens, Ohio 43, Streetsboro, OH, USA
April 28, 2021 5:52 PM
“Got the first dose of the Pfizer vaccine yesterday at Walgreens. Process was very smooth, no allergic reactions. Had some initial wooziness and lightheadedness 5 minutes after receiving the vaccine but may have just been anxiety.
Symptoms after 27 hours: sore arm, joint and muscle pain, fatigue.... Feeling warm/flushed but no fever. ”
Fort Smith, AR, USA
April 30, 2021 3:56 PM
“The same still saw scam as the other people on here. Same ad. It states $19.99 for that day and I ordered it. I also got the little manual wire saw. It said saw and accessories. It really hurts people on a fixed income. I hope they are proud of themselve ”
Symptoms: Other Headache
Lauderhill, Florida, USA
April 25, 2021 12:35 PM
“I am having side effects. the left side of my mouth moves by it self, and air comes out. it did it back to back. my head and neck was hurting. also at times my beath stops for a brife second. these things never happened before. should i go to the hospital ”
Kingston, ON, Canada
April 29, 2021 10:25 AM
““I purchased this Stihl chain saw on Feb 4, 2021 from Blackcass but to date all I received was a chain with grips. I would like my saw as ordered or a full refund and they pay for shipping. ”
Kibbles and bits bistro, Walmart Supercenter, South Oates Street, Dothan, AL, USA, Walmart Supercenter, South Oates Street, Dothan, AL, USA
Walmart Supercenter, South Oates Street, Dothan, AL, USA
April 18, 2021 10:04 AM
“I have 2 sick, A week and a half ago Née bag of Kibbles and bits bistro and the Melody Just started about a week and a half ago now I have two dogs sick one with an IV in the hospital ”
Doctor Visit: Yes
Tenacore LLC 2001 Tenacore Replacement CareFusion Alaris 8100 bezels - recalled due to Potentially weakened elastic, USA
April 19, 2021 9:01 PM
“Company name: Tenacore LLC
Brand name: Tenacore LLC
Product recalled: 2001 Tenacore Replacement CareFusion Alaris 8100 bezels
Reason of the recall: Potentially weakened elastic
FDA Recall date: April 19, 2021
Recall details: Company Announcement On February 24th, 2021, Tenacore LLC initiated a... nationwide recall of 2001 Tenacore replacement CareFusion Alaris 8100 bezels due to potentially weakened plastic. A bezel with weakened plastic may, over time, lead to separation of the bezel post (recall issue) as well as other damage to the bezel (e.g., external cracking). The separation of one or more bezel posts may result in free flow, over infusion, under infusion or interruption of infusion. There is a related recall initiated by Becton Dickinson (BD). Information regarding that recall can be found using the following link: Becton Dickinson (BD) (CareFusion 303, Inc.) Recalls Alaris Pump Module Model 8100 Bezel Assembly Which Could Result in Free Flow, Over-Infusion, Under-Infusion, or Interruption of Infusion | FDA Consumers who have: Tenacore bezel parts (part number TIPA-8100-4410) with timestamp 5 and/or timestamp 6 should stop the distribution and use of these and return them to Tenacore LLC.
Alaris 8100 units that were serviced by Tenacore, or purchased from Tenacore between July 2020 and Feb 2020, should be inspected per the instructions described below to ensure that your device is not impacted. If it is, please return your device to Tenacore LLC.
Recalled bezels were manufactured from May 2020 to June 2020 and distributed from July 2020 through Feb 2021. The following products have been recalled:
Check the full recall details on fda.gov
Source: FDA ”
Fort Myers, FL, USA
May 10, 2021 1:47 PM
“I ordered two of the Outdoor orange saws off of fb on March I have not received either one. Invoice #489-10127461
Transaction # 1ym4274N33939154. I really need them as they were gifts. One of them was my husband's birthday present at the end of March They were ordered early and they removed t... he money from my account March 6, 2021. They still show them on FB. They also sent that email to me. After checking with others, information is not correct. Never delivered. ”