FoodNov 2, 2022
Cuisine Innovations Unlimited Earth Grown Vegan Traditional Falafel NET WT 12 OZ recall — FDA F-0140-2023
Possible presence of Shiga toxin-producing E. coli.
Class IFDA: TerminatedCuisine Innovations Unlimited, 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 25
Records are ordered by the best available source date.
FoodNov 2, 2022
Secrets Of The Tribe Indian Gooseberry Alcohol-Free Extract, 2 oz recall — FDA F-0073-2023
Product has elevated level of lead.
Class IIFDA: TerminatedSecrets Of The Tribe
FoodNov 2, 2022
Cuisine Innovations Unlimited Earth Grown Vegan Garlic & Herb Falafel NET WT 12 OZ recall — FDA F-0141-2023
Possible presence of Shiga toxin-producing E. coli.
Class IFDA: TerminatedCuisine Innovations Unlimited, LLC
FoodNov 2, 2022
Tomoorona Qassim Mix for Coffee, Net Weight 125g, packaged in a plastic recall — FDA F-0077-2023
The product is labeled to contain sodium caseinate, a milk derivative, but the label does not declare the product contains "milk."
Class IIFDA: TerminatedTomoorona LLC
DrugNov 2, 2022
Ultra Chem Labs Proton Armor, Anti-Microbial Alcohol-Free Foaming Hand Sanitizer, kills recall — FDA D-0016-2023
Chemical Contamination and CGMP Deviations: trace amounts of methanol found in one of the components during the manufacturing process.
Class IIFDA: TerminatedUltra Chem Labs Corp
DrugNov 2, 2022
Exela Pharma Sciences 8.4% Sodium Bicarbonate Injection, USP 50 mEq/50 mL (1 mEq/mL) 50 mL recall — FDA D-0023-2023
Defective Container: Complaints received of vial breakage and glass flying when pressurized while preparing the product for administration
Class IFDA: TerminatedExela Pharma Sciences LLC
DrugNov 2, 2022
SODIUM BICARBONATE 8.4% Sodium Bicarbonate Injection, USP 50 mEq/50 mL (1 mEq/mL) 50 mL recall — FDA D-0022-2023
Defective Container: Complaints received of vial breakage and glass flying when pressurized while preparing the product for administration
Class IFDA: TerminatedExela Pharma Sciences LLC
DrugNov 2, 2022
Ultra Chem Labs Proton Armor, Anti-Microbial Alcohol-Free Foaming Hand Sanitizer, kills recall — FDA D-0017-2023
Chemical Contamination and CGMP Deviations: trace amounts of methanol found in one of the components during the manufacturing process.
Class IIFDA: TerminatedUltra Chem Labs Corp
DrugNov 2, 2022
Fondaparinux Sodium Injection, USP, 7.5 mg per 0.6 mL, Single Dose, Prefilled Syringe recall — FDA D-0020-2023
Subpotent Drug: Out of specification for assay
Class IIFDA: TerminatedAuroMedics Pharma LLC
VehicleNov 2, 2022
BMW windshield recall — NHTSA campaign 22V820000
BMW of North America, LLC (BMW) is recalling certain 2023 X5 sDrive40i, xDrive40i, xDrive45e, and X7 xDrive40i vehicles. The windshield may not have been properly bonded to the vehicle…
windshieldBMW of North America, LLC
VehicleNov 1, 2022
Tesla exterior recall — NHTSA campaign 22E092000
Tesla, Inc. (Tesla) is recalling certain 2021 Model S exterior side rearview mirrors, part numbers: 1622232-00-B and 1622233-00-B. The driver side exterior rearview mirrors are convex…
exteriorTesla, Inc.
VehicleNov 1, 2022
Tesla electric power assist system recall — NHTSA campaign 22V818000
Tesla, Inc. (Tesla) is recalling certain 2017-2021 Model S and Model X vehicles. The electronic power assist steering (EPAS) system may experience a loss of power steering assist when…
electric power assist systemTesla, Inc.
VehicleOct 31, 2022
Volkswagen Group of pressure monitoring and regulating systems recall — NHTSA campaign 22V815000
Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2019 Volkswagen Tiguan LWB, Golf Sportswagen A7, Golf Alltrack, Golf R GP, Audi Q3, Audi A3 Cabriolet, 2019-2020 Jetta…
pressure monitoring and regulating systemsVolkswagen Group of America, Inc.
Medical DeviceOct 26, 2022
Synthes (USA) Products SPEED 15X12X12mm Continuous Compression Implant, Product No recall — FDA Z-0099-2023
The subject products are being recalled because they contain the incorrect size drill guide and will not prepare the bone correctly for the size of the implant included in the sterile kit.…
Class IIFDA: OngoingSynthes (USA) Products LLC
Medical DeviceOct 26, 2022
B. Braun Medical Extension Set, EXT SET W/CARESITE, 6IN., Product Code 470169, 50 units per recall — FDA Z-0091-2023
The extension set has a high probability of failure which could lead to possible leakage or detachment at the device's bonded joint during use. The issue may result in delay of therapy,…
Class IIFDA: OngoingB. Braun Medical, Inc.
Medical DeviceOct 26, 2022
Becton Dickinson & Company BD Vacutainer Tube Sodium Fluoride: 100 mg, Potassium Oxalate: 20 recall — FDA Z-0095-2023
The affected product contains isobutylene which has recently demonstrated potential interference in determination of methanol by gas chromatography methods. The interference may lead to…
Class IIFDA: OngoingBecton Dickinson & Company
Medical DeviceOct 26, 2022
Abbott Vascular Product/Part: MitraClip G4 CDS NT REPAIR-MR Clinical/CDS0704-NT, MitraClip recall — FDA Z-0117-2023
An increase in clip locking malfunctions, Establish Final Arm Angle and Clip Opening While Locked, have been observed. Contributing causes may be clip locking component material properties…
Class IIFDA: OngoingAbbott Vascular
Medical DeviceOct 26, 2022
B. Braun Medical ULTRASITE US04TL Smallbore T-Port Extension Set, Product Code 474515, 100 recall — FDA Z-0090-2023
The extension set has a high probability of failure which could lead to possible leakage or detachment at the device's bonded joint during use. The issue may result in delay of therapy,…
Class IIFDA: OngoingB. Braun Medical, Inc.
Medical DeviceOct 26, 2022
Abbott Vascular Product/Part: MitraClip NTR Clip Delivery System US/CDS0601-NTR, MitraClip recall — FDA Z-0116-2023
An increase in clip locking malfunctions, Establish Final Arm Angle and Clip Opening While Locked, have been observed. Contributing causes may be clip locking component material properties…
Class IIFDA: OngoingAbbott Vascular
Medical DeviceOct 26, 2022
Intersurgical Solus Standard, laryngeal mask airway, size 3, small adult, 30-50kg recall — FDA Z-0096-2023
Printing error on the device, size 3 Solus Standard laryngeal mask airway has been incorrectly marked with size 4 information (includes the number 4 as a size identifier, patient weight and…
Class IIFDA: TerminatedIntersurgical Inc.
Medical DeviceOct 26, 2022
Synthes (USA) Products SPEEDSHIFT20x20x20 Offset 10mm Implant Drill Kit, Product No recall — FDA Z-0098-2023
The subject products are being recalled because they contain the incorrect size drill guide and will not prepare the bone correctly for the size of the implant included in the sterile kit.…
Class IIFDA: OngoingSynthes (USA) Products LLC
Medical DeviceOct 26, 2022
B. Braun Medical CARESITE SMALLBORE EXT SET T-PORT 5 IN., Product Code 470114, 100 units per recall — FDA Z-0092-2023
The extension set has a high probability of potential failure which could lead to possible leakage or detachment at the device's bonded joint during use. The issue may result in delay of…
Class IIFDA: OngoingB. Braun Medical, Inc.
Medical DeviceOct 26, 2022
Siemens Healthcare Diagnostics Atellica CH Lithium_2 (LITH_2), Siemens Material Number recall — FDA Z-0104-2023
Potential for falsely elevated LITH_2 and Li results on the Atellica CH 930 Analyzer. In the worst case, there is a potential for erroneously elevated lithium patient results, which may…
Class IIFDA: OngoingSiemens Healthcare Diagnostics, Inc.
Medical DeviceOct 26, 2022
Synthes (USA) Products DePuy Synthes Hammertoe Continuous Compression Implants, Product No. recall — FDA Z-0101-2023
The subject products are being recalled because they contain the incorrect size drill guide and will not prepare the bone correctly for the size of the implant included in the sterile kit.…
Class IIFDA: OngoingSynthes (USA) Products LLC
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.