FoodAug 18, 2021
5000 Years Foods and 128 oz and 64 oz glass jars recall — FDA F-0850-2021
potential to be contaminated with Listeria monocytogenes
Class IIFDA: Terminated5000 Years Foods, Inc.
August 2021 recalls — page 8
These records include useful source details for the selected month.
FoodAug 18, 2021
McCormick Culinary Italian Seasoning 1.75 lbs recall — FDA F-0899-2021
Product may be contaminated with Salmonella.
Class IFDA: TerminatedMcCormick & Company - MSS - HQ
FoodAug 18, 2021
5000 Years Foods 64 oz, 32 oz, & 16 oz glass jars recall — FDA F-0855-2021
potential to be contaminated with Listeria monocytogenes
Class IIFDA: Terminated5000 Years Foods, Inc.
FoodAug 18, 2021
5000 Years Foods and 128 oz and 64 oz glass jars recall — FDA F-0852-2021
potential to be contaminated with Listeria monocytogenes
Class IIFDA: Terminated5000 Years Foods, Inc.
FoodAug 18, 2021
McCormick & Company - MSS - HQ Frank s Red Hot Buffalo Ranch Seasoning 153g, Plastic Bottles recall — FDA F-0900-2021
Product may be contaminated with Salmonella.
Class IFDA: TerminatedMcCormick & Company - MSS - HQ
FoodAug 18, 2021
5000 Years Foods NO MSG JULRADO WHOLE CABBAGE KIMCHI in 128 oz recall — FDA F-0854-2021
potential to be contaminated with Listeria monocytogenes
Class IIFDA: Terminated5000 Years Foods, Inc.
FoodAug 18, 2021
IHERB Solumeve Hydrolyzed Collagen Peptides, Turmeric + MCT and recall — FDA F-0846-2021
Informed by contract manufacturer that the MCT ingredient used in their product was under recall due to undeclared milk.
Class IFDA: TerminatedIHERB LLC
FoodAug 18, 2021
DSD Merchandisers Dark Chocolate Malt Balls in plastic container recall — FDA F-0871-2021
Firm notified by customers that product labeled as Dark Chocolate Malt Balls had Dark Chocolate Peanut Butter malt balls inside - undeclared peanuts.
Class IFDA: TerminatedDSD Merchandisers, Inc.
FoodAug 18, 2021
5000 Years Foods and 128 oz, 64 oz, 32 oz, & 16 oz glass jars recall — FDA F-0853-2021
potential to be contaminated with Listeria monocytogenes
Class IIFDA: Terminated5000 Years Foods, Inc.
DrugAug 18, 2021
Med Shop Total Care MORPHINE-BUPIVACAINE-KETAMINE PF INJECTABLE 21 mL syringe in two recall — FDA D-0713-2021
Non-Sterility
Class IFDA: TerminatedMed Shop Total Care Inc.
DrugAug 18, 2021
Nystatin Oral Suspension, USP 100,000 units per mL, Cherry/Peppermint Flavor recall — FDA D-0721-2021
Lack of CGMP: This recall is being carried out due to potential for carry over of Senna Syrup.
Class IIFDA: TerminatedPAI Holdings, LLC. dba Pharmaceutical Associates Inc.
DrugAug 18, 2021
Med Shop Total Care HYDROMORPHONE HCL-BUPIVACAINE HCL PF INJECTABLE 21 and 22 mL syringes in recall — FDA D-0717-2021
Non-Sterility
Class IFDA: TerminatedMed Shop Total Care Inc.
DrugAug 18, 2021
PAI Holdings, LLC. dba Pharmaceutical Associates Cimetidine Hydrochloride Oral Solution 300 recall — FDA D-0722-2021
Lack of CGMP: This recall is being carried out due to potential for carry over of Senna Syrup.
Class IIFDA: TerminatedPAI Holdings, LLC. dba Pharmaceutical Associates Inc.
DrugAug 18, 2021
Med Shop Total Care MORPHINE-BUPIVACAINE PF INJECTABLE 21 mL, 22 mL, 23 mL, 41 mL and 43 mL recall — FDA D-0710-2021
Non-Sterility
Class IFDA: TerminatedMed Shop Total Care Inc.
DrugAug 18, 2021
Med Shop Total Care HYDROMORPHONE HCL-BUPIVACAINE HCL-BACLOFEN PF INJECTABLE 21 mL syringes recall — FDA D-0708-2021
Non-Sterility
Class IFDA: TerminatedMed Shop Total Care Inc.
DrugAug 18, 2021
SUN PHARMACEUTICAL INDUSTRIES Venlafaxine Tablets, USP 50 mg*, 100 Tablets recall — FDA D-0703-2021
Presence of Forein Tablets/Capsules; Venlafaxine Tablets, USP 37.5 mg found in bottles labeled as Venlafaxine Tablets, USP, 50 mg
Class IIFDA: TerminatedSUN PHARMACEUTICAL INDUSTRIES Inc.
DrugAug 18, 2021
Eli Lilly & Company Zyprexa Intramuscular, Olanzapine for Injection, 10 MG per Single Use recall — FDA D-0720-2021
cGMP deviations: Atypical appearance, decrease in size and change in color of the lyophilized cake of drug product.
Class IIFDA: TerminatedEli Lilly & Company
DrugAug 18, 2021
Ethosuximide Oral Solution USP 250 mg/5 mL, 16 fl oz (473 mL) recall — FDA D-0723-2021
Lack of CGMP: This recall is being carried out due to potential for carry over of Senna Syrup.
Class IIFDA: TerminatedPAI Holdings, LLC. dba Pharmaceutical Associates Inc.
DrugAug 18, 2021
Med Shop Total Care HYDROMORPHONE HCL-BUPIVACAINE HCL-FENTANYL PF INJECTABLE 21 mL syringe recall — FDA D-0711-2021
Non-Sterility
Class IFDA: TerminatedMed Shop Total Care Inc.
DrugAug 18, 2021
Med Shop Total Care HYDROMORPHONE HCL-BUPIVACAINE HCL-CLONIDINE HCL PF INJECTABLE 21 mL recall — FDA D-0709-2021
Non-Sterility
Class IFDA: TerminatedMed Shop Total Care Inc.
VehicleAug 12, 2021
Chrysler curtain air bag inflator recall — NHTSA campaign 21V632000
Chrysler (FCA US, LLC) is recalling certain 2015-2020 Ram 1500 Classic, 2015-2016 Ram 3500, and Ram 2500 vehicles, and 2016 Ram 3500 Cab Chassis with a gross vehicle weight rating less than…
curtain air bag inflatorChrysler (FCA US, LLC)
Medical DeviceAug 11, 2021
Stanbio Laboratory Cardinal Health Beta-Hydroxybutyrate LiquiColor for Synchron CX/LX/DX. in recall — FDA Z-2203-2021
Deterioration in the stability of the reagents which has resulted in lower than expected or out of range Quality Control values.
Class IIIFDA: TerminatedStanbio Laboratory, LP
Medical DeviceAug 11, 2021
Abbott Laboratories REF 8L92-22, Abbott Activated Alanine aminotransferase, for use with recall — FDA Z-2185-2021
There is a potential for >10% under-recovery on Activated Alanine Aminotransferase (A-ALT) samples greater than 1,200 U/L. In addition there is a potential for a >10% shift in patient…
Class IIFDA: OngoingAbbott Laboratories
Medical DeviceAug 11, 2021
Abbott Laboratories REF 8L92-21, Abbott Activated Alanine Aminotransferase, for use with recall — FDA Z-2186-2021
There is a potential for >10% under-recovery on Activated Alanine Aminotransferase (A-ALT) samples greater than 1,200 U/L. In addition there is a potential for a >10% shift in patient…
Class IIFDA: OngoingAbbott Laboratories
How to use this monthly recall archive
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.