FoodNov 16, 2022
DA CHENG VEGETARIAN FOOD Vegan Golden Nuggets recall — FDA F-0138-2023
Vegan Golden Nuggets were sampled by the FDA and found to contain egg that is not declared on the label.
Class IFDA: TerminatedDA CHENG VEGETARIAN FOOD 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 19
Records are ordered by the best available source date.
FoodNov 16, 2022
RIVER CITY SEAFOOD INTERNATIONAL La Rosa Brand BluCrab Pasteurized Crabmeat recall — FDA F-0178-2023
Defective seal in cans containing pasteurized crabmeat.
Class IIFDA: TerminatedRIVER CITY SEAFOOD INTERNATIONAL LLC
FoodNov 16, 2022
Albertsons Companies Chicken Salad Sandwich Club 18 Inch Tray, Black tray with 16 recall — FDA F-0149-2023
Store printed label on products does not include Tree Nuts (Cashews) in the ingredient statement and the contains statement.
Class IFDA: TerminatedAlbertsons Companies LLC
FoodNov 16, 2022
Taylor Farms Retail BabyBel Snacker recall — FDA F-0143-2023
Allergens of almonds and milk not declared on the product ingredient label
Class IIFDA: TerminatedTaylor Farms Retail, Inc.
FoodNov 16, 2022
JLM Manufacturing JLM Sesame Sticks Mix in clear plastic 11oz recall — FDA F-0144-2023
Undeclared cashew
Class IIFDA: TerminatedJLM Manufacturing LLC
FoodNov 16, 2022
Shemshad Food Products 2 oz recall — FDA F-0134-2023
FDA sample revealed the product had higher than declared sodium content (131% of the net contents).
Class IIFDA: TerminatedShemshad Food Products, Inc.
FoodNov 16, 2022
Hammond's Candies Since 1920 II NET WT recall — FDA F-0146-2023
Peanut Butter Chocolate Chip Cookies mispacked in Salted Caramel Cookies Box creating undeclared peanut allergen.
Class IFDA: TerminatedHammond's Candies Since 1920 II, LLC
FoodNov 16, 2022
DA CHENG VEGETARIAN FOOD Vegan Golden Nuggets recall — FDA F-0139-2023
Vegan Golden nuggets were sampled by the FDA and found to contain egg that is not declared on the label.
Class IFDA: TerminatedDA CHENG VEGETARIAN FOOD Inc.
FoodNov 16, 2022
Bakkavor USA H-E-B Meal Simple Tomato Basil Soup 32 oz recall — FDA F-0135-2023
Bakkavor USA has initiated a recall of H-E-B Meal Simple Tomato Basil Soup, 32 oz. Plastic containers, 6 containers per case because of undeclared milk allergen.
Class IFDA: TerminatedBakkavor USA, Inc.
DrugNov 16, 2022
Octreotide Acetate Injection 500 mcg/mL, 10 x 1 mL Single-Dose Unit-of-Use Syringes, For recall — FDA D-0058-2023
Presence of Particulate Matter: Product complaint for the presence of glass particles in a syringe.
Class IFDA: TerminatedViatris Inc.
VehicleNov 15, 2022
Model X air bag control module software recall — NHTSA campaign 22V843000
Tesla, Inc. (Tesla) is recalling certain 2021-2023 Model X vehicles. The restraint control module (RCM) calibration may cause the front passenger air bag to deploy incorrectly during…
air bag control module softwareTesla, Inc.
VehicleNov 15, 2022
F-150 motor recall — NHTSA campaign 22V842000
Ford Motor Company (Ford) is recalling certain 2021-2022 F-150 vehicles. The front windshield wiper motor may become inoperative, causing the wipers to fail.
motorFord Motor Company
VehicleNov 15, 2022
Tesla tail lights recall — NHTSA campaign 22V844000
Tesla, Inc. (Tesla) is recalling certain 2023 Model 3 and 2020-2023 Model Y vehicles. One or both taillights may intermittently fail to illuminate.
tail lightsTesla, Inc.
VehicleNov 10, 2022
Chrysler automatic transmission recall — NHTSA campaign 22V835000
FCA US, LLC (Chrysler) is recalling certain 2020-2023 Ram 2500 and 2020-2022 Ram 3500 vehicles. A build-up of pressure and heat inside the transmission may result in a transmission fluid…
automatic transmissionChrysler (FCA US, LLC)
Medical DeviceNov 9, 2022
Becton, Dickinson and Company, BD Biosciences BD Trucount Tubes recall — FDA Z-0171-2023
Due to partial label detachment on tubes. This can cause tubes to become stuck together in the pouch or cause automation errors when used with the automated loader for the wash assistant.…
Class IIFDA: OngoingBecton, Dickinson and Company, BD Biosciences
Medical DeviceNov 9, 2022
Edwards Lifesciences Fogarty Biliary Balloon Probes recall — FDA Z-0147-2023
Due to an increase of confirmed latex deterioration complaints for arterial embolectomy catheters packaged in pouches.
Class IIFDA: OngoingEdwards Lifesciences, LLC
Medical DeviceNov 9, 2022
Baxter Healthcare Beach Chair Clamp, BEACH CHAIR SHLDER POSITIONER CMPT, REF A-90013 recall — FDA Z-0178-2023
the adhesive, applied to screws and bolts as an additional holding force, may not cure correctly, and as a result, could result in a loss of holding and reduced mechanical integrity.
Class IIFDA: TerminatedBaxter Healthcare Corporation
Medical DeviceNov 9, 2022
Baxter Healthcare C-Flex Polar Head Positnr-Device Only, SSP-NEUROSURGICAL HEADREST, REF recall — FDA Z-0176-2023
the adhesive, applied to screws and bolts as an additional holding force, may not cure correctly, and as a result, could result in a loss of holding and reduced mechanical integrity.
Class IIFDA: TerminatedBaxter Healthcare Corporation
Medical DeviceNov 9, 2022
Baxter Healthcare Hillrom Hospital Bed Accessory, WatchCare Incontinence Management System recall — FDA Z-0144-2023
Radio frequency emission from a functioning WatchCare device may potentially impact other devices (including, but not limited to telemetry devices, bladder scanner, fetal monitor/doppler,…
Class IFDA: OngoingBaxter Healthcare Corporation
Medical DeviceNov 9, 2022
Baxter Healthcare Allen Life Assist Beach Chair, BCSSP-BEACH CHAIR , REF A-91501, #104002 recall — FDA Z-0179-2023
the adhesive, applied to screws and bolts as an additional holding force, may not cure correctly, and as a result, could result in a loss of holding and reduced mechanical integrity.
Class IIFDA: TerminatedBaxter Healthcare Corporation
Medical DeviceNov 9, 2022
Baxter Healthcare Allen Advance Table, RSP-ADVANCE TABLE: a) REF A-71100-US, #107003, b) recall — FDA Z-0175-2023
the adhesive, applied to screws and bolts as an additional holding force, may not cure correctly, and as a result, could result in a loss of holding and reduced mechanical integrity.
Class IIFDA: TerminatedBaxter Healthcare Corporation
Medical DeviceNov 9, 2022
Baxter Healthcare Hillrom Hospital Bed Accessory, Watch Care Incontinence Management System recall — FDA Z-0145-2023
Radio frequency emission from a functioning WatchCare device may potentially impact other devices (including, but not limited to telemetry devices, bladder scanner, fetal monitor/doppler,…
Class IFDA: OngoingBaxter Healthcare Corporation
Medical DeviceNov 9, 2022
MEDLINE INDUSTRIES, LP - Northfield BAUSCH + LOMB EYE MUSCLE, REF VAL036EMESB recall — FDA Z-0159-2023
Medline received complaints on some of the breather pouches with in the sterile surgical kits show openings in the seal.
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceNov 9, 2022
MEDLINE INDUSTRIES, LP - Northfield BAUSCH + LOMB CATARACT PACK, REF VAL009CTSGA recall — FDA Z-0158-2023
Medline received complaints on some of the breather pouches with in the sterile surgical kits show openings in the seal.
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
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.