FoodJun 22, 2022
Cedar Crest Specialties Net Wt recall — FDA F-1296-2022
Foreign material - plastic
Class IIFDA: TerminatedCedar Crest Specialties, Inc.
Monthly breakdown
2022 recalls by month
Select a month to review the recall records reported during that period.
December 2022318 records · 4 categoriesNovember 2022270 records · 4 categoriesOctober 2022288 records · 4 categoriesSeptember 2022318 records · 4 categoriesAugust 2022293 records · 4 categoriesJuly 2022334 records · 4 categoriesJune 2022348 records · 4 categoriesMay 2022227 records · 4 categoriesApril 2022205 records · 4 categoriesMarch 2022449 records · 4 categoriesFebruary 2022237 records · 4 categoriesJanuary 2022296 records · 4 categories
2022 recalls — page 80
Records are ordered by the best available source date.
FoodJun 22, 2022
Deskins Wholesale Peanut Butter No Bake,16 oz., Plastic Shell, 12-16oz recall — FDA F-1311-2022
Products were made with peanut butter contaminated with Salmonella.
Class IFDA: TerminatedDeskins Wholesale, LLC
FoodJun 22, 2022
White Cane Sockeye Salmon Wild Alaskan Cooked and Smoked Salmon, brand White Cane recall — FDA F-1305-2022
Label declares Teriyaki Sauce but does not declare Wheat and Soy.
Class IIFDA: TerminatedWhite Cane Sockeye Salmon LLC
FoodJun 22, 2022
A G Specialty Foods Keep Refrigerated recall — FDA F-1301-2022
Potential contamination with Salmonella.
Class IFDA: TerminatedA G Specialty Foods Inc.
FoodJun 22, 2022
Morski Brands Ranch BLT Pasta Salad, Keep Refrigerated packaged in the recall — FDA F-1374-2022
Foreign object (metal).
Class IIFDA: TerminatedMorski Brands, Inc.
FoodJun 22, 2022
Bix Produce Company Egg &Cheese Curd Snack/Power Box recall — FDA F-1285-2022
Potential Salmonella contamination.
Class IFDA: TerminatedBix Produce Company LLC
FoodJun 22, 2022
Morski Brands Steakhouse Potato Salad, Keep Refrigerated packaged in the recall — FDA F-1373-2022
Foreign object (metal).
Class IIFDA: TerminatedMorski Brands, Inc.
FoodJun 22, 2022
Thistle Watermelon Berry Cold-Pressed Organic Juice watermelon recall — FDA F-1313-2022
Manufactured using organic strawberries potentially contaminated with Hep A.
Class IIFDA: TerminatedTHISTLE HEALTH Inc.
FoodJun 22, 2022
Soul Cedar Farm Zesty Sweet Peppers recall — FDA F-1298-2022
Potential to be contaminated with Clostridium botulinum. Product was tested and found to have pH level of 5.57.
Class IIFDA: TerminatedSoul Cedar Farm LLC
FoodJun 22, 2022
Deskins Wholesale Peanut Butter Fudge,16 oz., Plastic Shell, 12 - 16oz recall — FDA F-1310-2022
Products were made with peanut butter contaminated with Salmonella.
Class IFDA: TerminatedDeskins Wholesale, LLC
FoodJun 22, 2022
Deskins Wholesale Peanut Butter Pinwheel ,16 oz., Plastic Shell, 12-16oz recall — FDA F-1309-2022
Products were made with peanut butter contaminated with Salmonella.
Class IFDA: TerminatedDeskins Wholesale, LLC
FoodJun 22, 2022
Abbott Laboratories Pedialyte***Replaces Electrolytes***Great for Kids and recall — FDA F-1312-2022
The third party contract manufacturer used a dextrose ingredient derived from wheat in one lot of the Strawberry Lemonade powder, which is not declared on the label.
Class IIIFDA: TerminatedAbbott Laboratories
DrugJun 22, 2022
Washington Homeopathic Products Candida Albicans, Potency: 9C, 10C, 12C, 13C, 14C 15C 16C recall — FDA D-1127-2022
cGMP deviations
Class IIFDA: TerminatedWashington Homeopathic Products, Inc.
DrugJun 22, 2022
SUN PHARMACEUTICAL INDUSTRIES medroxyPROGESTERone Acetate Injectable Suspension, USP, 1 mL recall — FDA D-1143-2022
Lack of assurance of sterility
Class IIFDA: TerminatedSUN PHARMACEUTICAL INDUSTRIES Inc.
DrugJun 22, 2022
HAND SANITIZER SAY GOODBYE TO GERMS Alcohol Antiseptic 80% Topical Non-Sterile Solution, 12 recall — FDA D-1149-2022
CGMP Deviations: FDA analysis found product to contain acetaldehyde and acetal above specification limits.
Class IIFDA: TerminatedHand Sanitizer LLC
DrugJun 22, 2022
AMS Packaging Premium Nature Instant Hand Sanitizer, (ethyl alcohol 65%), 8 oz/ 236 ML recall — FDA D-1148-2022
Subpotent Drug: FDA analysis has revealed some bottles of these products were sub potent for ethanol.
Class IIFDA: OngoingAMS Packaging Inc.
DrugJun 22, 2022
Walmart Artri King Reforzado con Ortiga Omega 3 Tablets, ORIGINAL, 100-count bottles recall — FDA D-1157-2022
Marketed Without An Unapproved NDA/ANDA: Product lot found to be tainted with undeclared diclofenac, an FDA approved nonsteroidal anti-inflammatory drug (NSAID) for the treatment of pain…
Class IFDA: CompletedWalmart Inc.
DrugJun 22, 2022
SUN PHARMACEUTICAL INDUSTRIES medroxyPROGESTERone Acetate Injectable Suspension, USP, 1 mL recall — FDA D-1146-2022
Lack of assurance of sterility
Class IIFDA: TerminatedSUN PHARMACEUTICAL INDUSTRIES Inc.
DrugJun 22, 2022
A.P. Nonweiler Alcohol Antiseptic 80%, Topical Solution, Hand Sanitizer, Non-Sterile recall — FDA D-1142-2022
CGMP Deviations: FDA analysis found product to contain acetaldehyde and acetal above specification limits.
Class IIFDA: OngoingA.P. Nonweiler
DrugJun 22, 2022
medroxyPROGESTERone Acetate Injectable Suspension, USP, 1 mL Prefilled Syringe, 150 mg/mL recall — FDA D-1145-2022
Lack of assurance of sterility
Class IIFDA: TerminatedSUN PHARMACEUTICAL INDUSTRIES Inc.
DrugJun 22, 2022
Lupin Pharmaceuticals Zileuton Extended-Release Tablets, 600 mg, 120-count bottle recall — FDA D-1150-2022
Failed Dissolution Specifications: Out of specification test results observed in dissolution testing during long term stability study.
Class IIFDA: TerminatedLupin Pharmaceuticals Inc.
DrugJun 22, 2022
SUN PHARMACEUTICAL INDUSTRIES medroxyPROGESTERone Acetate Injectable Suspension, USP, 25 x 1 recall — FDA D-1147-2022
Lack of assurance of sterility
Class IIFDA: TerminatedSUN PHARMACEUTICAL INDUSTRIES Inc.
DrugJun 22, 2022
SUN PHARMACEUTICAL INDUSTRIES medroxyPROGESTERone Acetate Injectable Suspension, USP, 1 mL recall — FDA D-1144-2022
Lack of assurance of sterility
Class IIFDA: TerminatedSUN PHARMACEUTICAL INDUSTRIES Inc.
DrugJun 22, 2022
Walmart Artri King Reforzado con Ortiga Omega 3 Tablets, ORIGINAL, a) 100-count bottles recall — FDA D-1159-2022
Marketed Without An Unapproved NDA/ANDA: All lots were found to be unapproved drugs based on labeling claims.
Class IIFDA: CompletedWalmart Inc.
About the 2022 recall archive
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.