FoodJul 6, 2022
Stellex/CF Houston Snack Fresh Apples and Peanut Butter Net Wt 6.5 oz recall — FDA F-1360-2022
Potential to be contaminated with Salmonella
Class IFDA: TerminatedStellex/CF Houston, LLC
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 76
Records are ordered by the best available source date.
FoodJul 6, 2022
Stellex/CF Houston Snack Fresh Apple & Cheese Bites with Crackers Net Wt recall — FDA F-1361-2022
Potential to be contaminated with Salmonella
Class IFDA: TerminatedStellex/CF Houston, LLC
FoodJul 6, 2022
Stellex/CF Houston Wegman's Apple, Pretzels & Cheese with Peanut Butter Net Wt recall — FDA F-1364-2022
Potential to be contaminated with Salmonella
Class IFDA: TerminatedStellex/CF Houston, LLC
FoodJul 6, 2022
Stellex/CF Houston Giant Apples, Pretzels & Celery with peanut butter Net Wt recall — FDA F-1363-2022
Potential to be contaminated with Salmonella
Class IFDA: TerminatedStellex/CF Houston, LLC
FoodJul 6, 2022
Klondike Cheese Company Boar's Head Brand Spinach Greek Yogurt Dip recall — FDA F-1383-2022
Foreign Object - plastic
Class IIFDA: TerminatedKlondike Cheese Company
FoodJul 6, 2022
Stellex/CF Houston Snack Sensations Apple, Pretzel & Celery Bites with Peanut recall — FDA F-1362-2022
Potential to be contaminated with Salmonella
Class IFDA: TerminatedStellex/CF Houston, LLC
FoodJul 6, 2022
Taylor Farms Florida Wawa Apples & Peanut Butter dipper 4.9oz recall — FDA F-1380-2022
Possible contamination with Salmonella.Products contains JM Smucker's Jif To Go Natural creamy peanut butter spread NET WT 1.5oz (43g) cups.
Class IFDA: TerminatedTaylor Farms Florida, Inc.
FoodJul 6, 2022
Safeway Fresh Foods Quick Chek, #14294 Apples and Peanut Butter Snack Tray, each recall — FDA F-1379-2022
Product was made with peanut butter that is potentially contaminated with Salmonella.
Class IFDA: TerminatedSafeway Fresh Foods LLC
FoodJul 6, 2022
Honey Heaven Wholesale The content inside package is walnut but was mis-labeled as recall — FDA F-1372-2022
Walnut package is mis-labeled as Nutritional Yeast and Walnuts are visible through clear package
Class IIFDA: TerminatedHoney Heaven Wholesale Inc.
FoodJul 6, 2022
Independent Beverage Company PurAqua Belle Vie SPARKLING WATER wellness RELAX 100mg recall — FDA F-1387-2022
Firm indicated that the product contains undeclared caffeine.
Class IIFDA: TerminatedIndependent Beverage Company LLC
DrugJul 6, 2022
Losartan potassium & Hydrochlorothiazide Tablets 100 mg/25 mg, 30, 90 & 1000 count NDC # recall — FDA D-1164-2022
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Class IIFDA: TerminatedMacleods Pharma Usa Inc.
DrugJul 6, 2022
Akcea Therapeutics Tegsedi (inotersen) Injection 284 mg/1.5 mL recall — FDA D-1166-2022
Superpotent: High Out of specification (OOS) test result for percent label claim (%LC).
Class IFDA: TerminatedAkcea Therapeutics, Inc.
DrugJul 6, 2022
Losartan Potassium Tablets, USP 25 mg, 90 Tablets bottles recall — FDA D-1161-2022
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Class IIFDA: TerminatedPD-Rx Pharmaceuticals, Inc.
DrugJul 6, 2022
Akorn Calcipotriene Topical Solution, 0.005% (Scalp Solution) recall — FDA D-1170-2022
Defective Delivery System: Potential defect that could prevent the product from dispensing as intended.
Class IIFDA: TerminatedAkorn, Inc.
DrugJul 6, 2022
Buzzagogo Allergy Bee Gone for Kids Nasal Swab Remedy 0.33 FL OZ (10 mL) tubes, UPC Code recall — FDA D-1160-2022
Microbial contamination of non-sterile product: FDA laboratory analysis found product to contain elevated levels of yeast and mold as well as the presence of Bacillus cereus.
Class IFDA: TerminatedBuzzagogo, LLC
DrugJul 6, 2022
Daytrana recall — FDA D-1169-2022
Defective Delivery System: Customer complaints received for ripping patches and tight release/adhesive transfer.
Class IIFDA: OngoingNoven Pharmaceuticals Inc.
DrugJul 6, 2022
Losartan Potassium Tablets, USP 100 mg, 90 Tablets bottles recall — FDA D-1163-2022
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Class IIFDA: TerminatedPD-Rx Pharmaceuticals, Inc.
DrugJul 6, 2022
Losartan Potassium Tablets, USP 50 mg, 90 Tablets bottles recall — FDA D-1162-2022
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Class IIFDA: TerminatedPD-Rx Pharmaceuticals, Inc.
DrugJul 6, 2022
Green Pharmaceuticals SnoreStop NasoSpray, 0.3 FL OZ (9 mL), Green Pharmaceuticals Inc recall — FDA D-1165-2022
Microbial contamination of non-sterile product: FDA laboratory analysis found product to contain microbial contamination identified as Providencia rettgeri.
Class IFDA: TerminatedGreen Pharmaceuticals, Inc.
VehicleJul 6, 2022
4Runner labels recall — NHTSA campaign 22V480000
Southeast Toyota Distributors, LLC (SET) is recalling certain 2020-2022 4Runner vehicles equipped with 20-inch Black Gunner Wheels. The load carrying capacity modification labels are…
labelsSoutheast Toyota Distributors, LLC
VehicleJul 1, 2022
Outback engine control module (ecu/ecm) recall — NHTSA campaign 22V473000
Subaru of America, Inc. (Subaru) is recalling certain 2022 Outback vehicles. The engine wiring harness may have been damaged, resulting in a loose electrical connection to the engine…
engine control module (ecu/ecm)Subaru of America, Inc.
VehicleJun 30, 2022
General Motors brake lights recall — NHTSA campaign 22V463000
General Motors (GM) has decided that certain 2022 model year Chevrolet Silverado, and GMC Sierra vehicles equipped with an accessory sport bar. The accessory sport bar contains a…
brake lightsGeneral Motors, LLC
Medical DeviceJun 29, 2022
Getinge Usa Sales Flow-e Anesthesia System : Intended for use in administering anesthesia recall — FDA Z-1279-2022
Potential for crack to form on the on/off switch of the suction unit, which may result in an unreasonable risk of harm to the patient. In the worst case, the switch can break, preventing…
Class IFDA: TerminatedGetinge Usa Sales Inc.
Medical DeviceJun 29, 2022
CardioTek EP-TRACER Software V2.x recall — FDA Z-1283-2022
Device did not pass electrical safety testing for adequate insulation.
Class IIFDA: CompletedCardioTek BV
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.