FoodApr 6, 2022
Tova Industries Carbquik Mug Cakes Cinnamon Spice, Net Wt recall — FDA F-0914-2022
Undeclared Allergen- Milk
Class IIFDA: TerminatedTova Industries 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 109
Records are ordered by the best available source date.
FoodApr 6, 2022
Suntree Snack Foods Good & Gather Dried Sweetened Strawberries recall — FDA F-0960-2022
Product contains undeclared Sulfites.
Class IIFDA: TerminatedSuntree Snack Foods, LLC
FoodApr 6, 2022
Lehi Valley Trading Co Woody's Smokehouse brand Yogurt Raisins, 12.3 oz recall — FDA F-0910-2022
Bags and tubs of yogurt covered raisins contained undeclared peanuts.
Class IFDA: TerminatedLehi Valley Trading Co, Inc.
DrugApr 6, 2022
Clotrimazole and Betamethasone Dipropionate Cream USP, 1%/0.05%,15 g tubes recall — FDA D-0727-2022
Failed Content Uniformity Specifications: Out-of-specification result for the Betamethasone Dipropionate assay of a stability sample
Class IIIFDA: TerminatedTaro Pharmaceuticals U.S.A., Inc.
DrugApr 6, 2022
Glycopyrrolate Tablets, USP, 1 mg, 100-count bottle recall — FDA D-0736-2022
Presence of Foreign Substance: Complaint for pieces of glass discovered in a sealed bottle which came from equipment within the packaging room.
Class IIFDA: TerminatedAurolife Pharma, LLC
DrugApr 6, 2022
Meclizine Hydrochloride Tablets USP, 12.5 mg recall — FDA D-0767-2022
Labeling: Label mix-up: Incorrect label placed on product. Shipper cases labeled Meclizine Hydrochloride Tablets contain bottles incorrectly labeled as PredniSONE Tablets. The tablets in…
Class IFDA: TerminatedJubilant Cadista Pharmaceuticals, Inc.
DrugApr 6, 2022
Drug Depot, Inc., dba APS Pharmacy TESTOSTERONE CYPIONATE/ ANASTROZOLE *GS* OIL (10ML) recall — FDA D-0731-2022
Lack of sterility assurance.
Class IIFDA: TerminatedDrug Depot, Inc., dba APS Pharmacy
VehicleApr 6, 2022
Volkswagen Group of body recall — NHTSA campaign 22V226000
Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2022 Tiguan and 2018-2021 Tiguan long wheel base (LWB) vehicles. Due to incorrect installation instructions, the…
bodyVolkswagen Group of America, Inc.
VehicleApr 1, 2022
Hyundai Motor front recall — NHTSA campaign 22V218000
Hyundai Motor America (Hyundai) is recalling certain 2021-2022 Elantra and 2020 Accent vehicles. In the event of a crash, the front driver and passenger-side seat belt pretensioners may…
frontHyundai Motor America
VehicleMar 31, 2022
General Motors curtain recall — NHTSA campaign 22V210000
General Motors, LLC (GM) is recalling certain 2020-2022 Chevrolet Traverse and 2021-2022 Buick Enclave vehicles. The harness connector to the left or right side roof rail air bag may have…
curtainGeneral Motors, LLC
Medical DeviceMar 30, 2022
Dignitana DigniCap Delta Scalp Cooling System, Product Number: 900-1001, Labeling: The recall — FDA Z-0825-2022
Instructions for Use (IFUs) updated to include use of a headband is now recommended for all patients and instructions for the application of the headband. Additionally, IFU updated to…
Class IIFDA: TerminatedDignitana, Inc.
Medical DeviceMar 30, 2022
Philips Respironics Trilogy 100, Trilogy 200, Garbin Plus, Aeris, LifeVent Continuous recall — FDA Z-0785-2022
In 2018, Philips Respironics added foam replacement to the preventive maintenance schedule for these devices after discovering the polyester-based polyurethane (PE-PUR) foam may degrade…
Class IFDA: OngoingPhilips Respironics, Inc.
Medical DeviceMar 30, 2022
Philips Healthcare Azurion systems with software release R2.0.x recall — FDA Z-0734-2022
In the Azurion system, the user can add a new study to a patient by selecting the option "Add Study". The Add Study dialogue box is then displayed where the Patient Type is selected to…
Class IIFDA: CompletedPhilips Healthcare
Medical DeviceMar 30, 2022
Baxter Healthcare Compella Bariatric Bed System recall — FDA Z-0820-2022
Potential damage to the power cord may cause the power conductors to be exposed, thereby creating a risk of shock from the power mains.
Class IIFDA: TerminatedBaxter Healthcare Corporation
Medical DeviceMar 30, 2022
B Braun Medical PERFUSOR SPACE - US VERSION recall — FDA Z-0819-2022
Units not properly inspected prior to release to the market, may not function as indicated in the product labeling, resulting in syringe detection and infusion accuracy that can result in…
Class IIFDA: TerminatedB Braun Medical Inc.
Medical DeviceMar 30, 2022
Integra LifeSciences Codman Cranial Access Kits- indicated when a craniotomy is required for recall — FDA Z-0817-2022
Incorrect extended expiration dates identified on the outer box label only, if product is used past the correct expiration date there is a potential for pain, infection, or adverse tissue…
Class IIFDA: TerminatedIntegra LifeSciences Corp.
Medical DeviceMar 30, 2022
Outset Tablo Console recall — FDA Z-0813-2022
Due to a component in the hemodialysis console there is the possibility of heat-related damage that may occur with the device.
Class IIFDA: OngoingOutset Medical, Inc.
Medical DeviceMar 30, 2022
BIOMET Trauma, [Item # 13182-22-26, DVR CROSSLOCK EXTRA LONG PLATE LEFT], [Item # recall — FDA Z-0810-2022
Packaging of various implants may not have sufficient adhesion on all sides, leading to loss of sterile barrier integrity. Use of product poses risk of infection, leading to surgical…
Class IIFDA: TerminatedBiomet, Inc.
Medical DeviceMar 30, 2022
BIOMET TRAUMA Drill Bit, Tap, Guide Pin: [DVR Drill Bit, Item # 212000022, DVR 2.2MM DRILL recall — FDA Z-0812-2022
Packaging of various implants may not have sufficient adhesion on all sides, leading to loss of sterile barrier integrity. Use of product poses risk of infection, leading to surgical…
Class IIFDA: TerminatedBiomet, Inc.
Medical DeviceMar 30, 2022
BIOMET Sports Medicine JUGGERLOC SLOTTED REAMER: [Item # 110010371, 6MM], [Item #110010372 recall — FDA Z-0809-2022
Packaging of various implants may not have sufficient adhesion on all sides, leading to loss of sterile barrier integrity. Use of product poses risk of infection, leading to surgical…
Class IIFDA: TerminatedBiomet, Inc.
Medical DeviceMar 30, 2022
Ace Surgical Supply Co NuOss Collagen Block Size 8mm x 9mm x 9mm- used in filling recall — FDA Z-0823-2022
NuOss Collagen (dental) was packaged with a Collatene Fibrillar Collagen(for oral wounds) rather than NuOss Collagen Block, may result in suboptimal bone repair
Class IIFDA: OngoingAce Surgical Supply Co., Inc.
Medical DeviceMar 30, 2022
BIOMET TRAUMA A.L.P.S recall — FDA Z-0811-2022
Packaging of various implants may not have sufficient adhesion on all sides, leading to loss of sterile barrier integrity. Use of product poses risk of infection, leading to surgical…
Class IIFDA: TerminatedBiomet, Inc.
Medical DeviceMar 30, 2022
Integra LifeSciences Codman Cranial Access Kits- indicated when a craniotomy is required for recall — FDA Z-0818-2022
Incorrect extended expiration dates identified on the outer box label only, if product is used past the correct expiration date there is a potential for pain, infection, or adverse tissue…
Class IIFDA: TerminatedIntegra LifeSciences Corp.
Medical DeviceMar 30, 2022
Dollar Tree Distribution Medical Device products purchased from Family Dollar retail stores recall — FDA Z-0822-2022
Potential exposure to rodents and rodent activity in the distribution center.
Class IIFDA: OngoingDollar Tree Distribution, 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.