Summary Company Announcement Date: May 18, 2021 FDA Publish Date: May 19, 2021 Product Type: Drugs Reason for Announcement: Recall Reason Description Presence of methanol Company Name: Dibar Nutricional S. de R.L. de C.V. Brand Name: Brand Name(s) DIBAR Labs, ProtectoRx Product Description: Product Description Hand Sanitizer Company Announcement Morelia, Michoacán, Mexico,Dibar Nutricional S. de…
Recall Expansion of Durisan Non-Alcohol Hand Sanitizer
Summary Company Announcement Date: May 14, 2021 FDA Publish Date: May 17, 2021 Product Type: Drugs Contaminants Reason for Announcement: Recall Reason Description Product is contaminated with Burkholderia contaminans Company Name: Sanit Technologies LLC d/b/a Durisan Brand Name: Brand Name(s) Product Description: Product Description Hand sanitizer Company Announcement Sanit Technologies LLC d/b/a Durisan is updating…
Novo Nordisk Issues Voluntary Nationwide Recall of Levemir®, Tresiba®, Fiasp®, Novolog® and Xultophy® Product Samples Due to Improper Storage Temperature Conditions
Summary Company Announcement Date: May 07, 2021 FDA Publish Date: May 10, 2021 Product Type: Drugs Reason for Announcement: Recall Reason Description Due to improper storage temperature conditions Company Name: Novo Nordisk Brand Name: Brand Name(s) Levemir, Tresiba, Fiasp, Novolog and Xultophy Product Description: Product Description Product Samples Company Announcement Novo Nordisk is voluntarily recalling…
Global Sanitizers Issues Voluntary Nationwide Recall of Medically Minded Hand Sanitizer Due to Presence of Undeclared Methanol
Summary Company Announcement Date: May 12, 2021 FDA Publish Date: May 13, 2021 Product Type: Drugs Reason for Announcement: Recall Reason Description Presence of methanol Company Name: Global Sanitizers Brand Name: Brand Name(s) Medically Minded Product Description: Product Description Hand Sanitizer Company Announcement Las Vegas, NV, Global Sanitizers is voluntarily recalling 50 thousand units of…
Abbott (formally known as “St. Jude Medical”) Recalls Assurity™ and Endurity™ Pacemakers for Potential Moisture Ingress Causing Electrical Short and Reduced Battery Life
The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death. Recalled Product Scalable Bradycardia Platform (SBP) Pacemakers: Assurity™ and Endurity™ Distribution Dates: April 29, 2015 to February 20, 2019 Devices Recalled in the U.S.: 61,973 Date Initiated by Firm:…
Scentsational Soaps & Candles, Inc. Voluntarily Expands Nationwide Recall of Scented Hand Sanitizers Due to the Presence of Methanol (Wood Alcohol), Benzene and Acetaldehyde
Summary Company Announcement Date: May 10, 2021 FDA Publish Date: May 13, 2021 Product Type: Drugs Reason for Announcement: Recall Reason Description Presence of Methanol (Wood Alcohol), Benzene and Acetaldehyde Company Name: Scentsational Soaps & Candles, Inc. Brand Name: Brand Name(s) Goose Creek, COCO TKO Product Description: Product Description Hand Sanitizer Company Announcement Scentsational Soaps…
Dibar Nutricional S. de R.L. De C.V. Issues Voluntary Nationwide Recall of DIBAR Labs Hand Sanitizer Due to the Presence of Methanol (Wood Alcohol)
Summary Company Announcement Date: May 11, 2021 FDA Publish Date: May 12, 2021 Product Type: Drugs Reason for Announcement: Recall Reason Description Presence of methanol Company Name: Dibar Nutricional S. de R.L. de C.V. Brand Name: Brand Name(s) DIBAR Labs, ProtectoRx Product Description: Product Description Hand Sanitizer Company Announcement Morelia, Michoacán, Mexico, Dibar Nutricional S….
Medtronic, Inc. Recalls Instructions for Use and Patient Manual for HeartWare HVAD System to Update Information about Carrying Case, Driveline Cover, and Controller Power-Up Issues
The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death. Recalled Product HeartWare HVAD System Instructions for Use and Patient Manual that accompany components including HeartWare HVAD Pump, Controller, Driveline Cable, Driveline Cover, and Surgical Tool Kits Models: HVAD…
Yamtun7 Issues Voluntary Nationwide Recall of Poseidon Platinum 3500 Due to the Presence of Undeclared Tadalafil and Sildenafil
Summary Company Announcement Date: May 11, 2021 FDA Publish Date: May 11, 2021 Product Type: Drugs Reason for Announcement: Recall Reason Description Undeclared Tadalafil and Sildenafil Company Name: Yamtun7 Brand Name: Brand Name(s) Product Description: Product Description Male Sexual Enhancement Dietary Supplement Company Announcement Delray Beach, Florida, Yamtun7 is voluntarily recalling all lots of Poseidon…
Hospira Issues A Voluntary Nationwide Recall for One Lot of 0.5% Bupivacaine Hydrochloride Injection, USP and One Lot of 1% Lidocaine HCl Injection, USP Due to Mislabeling
Summary Company Announcement Date: May 04, 2021 FDA Publish Date: May 04, 2021 Product Type: Drugs Reason for Announcement: Recall Reason Description Due to mislabeling Company Name: Hospira, Inc. Brand Name: Brand Name(s) Hospira, Inc. Product Description: Product Description 0.5% Bupivacaine Hydrochloride Injection, USP 30 mL and 1% Lidocaine HCl Injection, USP 30 mL Company…