FoodApr 19, 2023
Wellness Natural USA SimplyProtein Peanut Butter Chocolate Crispy 15-1.41 OZ recall — FDA F-0803-2023
Undeclared cashew
Class IIFDA: TerminatedWellness Natural USA Inc.
April 2023 recalls — page 4
These records include useful source details for the selected month.
FoodApr 19, 2023
Mutual Trading Company Kagome Worcester Sauce 6/60 fl oz recall — FDA F-0742-2023
Undeclared allergen; soy.
Class IFDA: TerminatedMutual Trading Company Inc.
FoodApr 19, 2023
Hiland Fat Free Chocolate Milk Vitamin A&D Naturally Flavored recall — FDA F-0716-2023
A small number of cartons may contain food grade sanitizer
Class IIFDA: TerminatedHiland Dairy Foods Company LLC
FoodApr 19, 2023
Scenic Fruit Company Simply Nature Organic Strawberries, frozen, net wt recall — FDA F-0705-2023
Potential to be contaminated with hepatitis A.
Class IFDA: TerminatedScenic Fruit Company, LLC
FoodApr 19, 2023
Scenic Fruit Company Frozen Organic Strawberries, Kirkland Signature, frozen, net recall — FDA F-0703-2023
Potential to be contaminated with hepatitis A.
Class IFDA: TerminatedScenic Fruit Company, LLC
FoodApr 19, 2023
Mutual Trading Company Kagome Chuno Sauce 30/10 fl oz Stock#24269 Ingredients recall — FDA F-0743-2023
Undeclared allergen; soy.
Class IFDA: TerminatedMutual Trading Company Inc.
FoodApr 19, 2023
Impossible Chicken Nuggets Made From Plants packaged in the recall — FDA F-0706-2023
Foreign Material (wood)
Class IIFDA: TerminatedImpossible Foods Inc.
FoodApr 19, 2023
Abbott Laboratories Zone Perfect Fudge Graham bar 50g bars packaged in foil recall — FDA F-0698-2023
Potential of foreign material (hard plastic) within product
Class IIFDA: TerminatedAbbott Laboratories
FoodApr 19, 2023
White Castle Chicken Slider Individual sandwiches packaged as recall — FDA F-0714-2023
Product packaged in incorrect labeling resulting in undeclared soy lecithin allergen
Class IIFDA: TerminatedWhite Castle System
DrugApr 19, 2023
Norepinephrine Bitartrate Injection, USP, 4 mg/4 mL* (1 mg/mL), 4 mL Single-dose Fliptop recall — FDA D-0529-2023
Failed Impurities/Degradation Specifications: Above the specification limits yielded for related substance norepinephrine sulfonic acid impurity during routine product monitoring.
Class IIIFDA: TerminatedSUN PHARMACEUTICAL INDUSTRIES Inc.
DrugApr 19, 2023
MEKTOVI (binimetinib) tablets, 15 mg, 180-count bottle recall — FDA D-0532-2023
Labeling: Incorrect or Missing Lot and/or Exp Date: The carton and bottle labels state an expiry date of March 2026; the correct expiration date is February 2025.
Class IIIFDA: OngoingPfizer Inc.
DrugApr 19, 2023
Pine Pharmaceuticals Bevacizumab 2.5 mg/0.1 mL, Solution for Injection in 1mL, silicone free recall — FDA D-0531-2023
Labeling: Incorrect or Missing Lot and/or Exp Date: Lot code on primary packaging is incorrect.
Class IIIFDA: TerminatedPine Pharmaceuticals, LLC
DrugApr 19, 2023
Epinephrine Professional EMS, Epinephrine Convenience Kit, Epinephrine 1 mg/mL recall — FDA D-0535-2023
Labeling; Incorrect NDC number on outer carton of product.
Class IIIFDA: OngoingFocus Health Group Inc.
VehicleApr 18, 2023
Mazda North American Operations control unit/module recall — NHTSA campaign 23V275000
Mazda North American Operations (Mazda) is recalling certain 2022-2023 CX-30 and 2023 CX-50 vehicles. The anti-lock brake system (ABS) Hydraulic Control Unit (HCU) may be damaged, which can…
control unit/moduleMazda North American Operations
VehicleApr 17, 2023
Nissan bead recall — NHTSA campaign 23V273000
Nissan North America, Inc. (Nissan) is recalling certain 2023 Titan and Frontier vehicles. The tires may have a tear in the inner bead which can cause a rapid loss of tire pressure.
beadNissan North America, Inc.
VehicleApr 13, 2023
Nissan critical fasteners recall — NHTSA campaign 23V268000
Nissan North America, Inc. (Nissan) is recalling certain 2023 Rogue, Pathfinder, and Infiniti QX60 vehicles. The driver's powered seat may not be fully secured to the seat frame, causing…
critical fastenersNissan North America, Inc.
VehicleApr 13, 2023
Ram 1500 control module (tcm/pcm/tecm) recall — NHTSA campaign 23V265000
Chrysler (FCA US, LLC) is recalling certain 2021 Ram 1500 vehicles equipped with 5.7L eTorque engines. The powertrain control module software may cause an incorrect fuel mixture condition…
control module (tcm/pcm/tecm)Chrysler (FCA US, LLC)
VehicleApr 13, 2023
Ram 1500 side impact recall — NHTSA campaign 23V264000
Chrysler (FCA US, LLC) is recalling certain 2022 Ram 1500 vehicles. The B-pillar impact sensors may be missing, which can result in delayed air bag deployment or non-deployment.
side impactChrysler (FCA US, LLC)
VehicleApr 13, 2023
Chrysler fuel pump recall — NHTSA campaign 23V263000
Chrysler (FCA US, LLC) is recalling certain 2021-2023 Jeep Wrangler, Gladiator, and 2022-2023 Ram 1500 vehicles equipped with a 3.0L diesel engine. The high pressure fuel pump (HPFP) may…
fuel pumpChrysler (FCA US, LLC)
Medical DeviceApr 12, 2023
Stryker Color Cuff Non-Sterile Disposable Tourniquet Cuff -NS DISP 18X4,1BLA,2PRT QUICK recall — FDA Z-1344-2023
Not able to achieve desired pressure and not holding pressure result from two different causes which have been reported to occur during initial set-up of the cuff onto the patient, may lead…
Class IIFDA: OngoingStryker Corporation
Medical DeviceApr 12, 2023
Medtronic Grafton Flex: a) DBM S42090 GRAFTON 1.5CM X 1.5CM FLEX, REF S42090 recall — FDA Z-1325-2023
Potential for packaging non-conformances directly related to the dual-barrier, sterile pouch packaging system. Non-conforming packaging may lead to a breach in the sterile barrier.
Class IIFDA: OngoingMedtronic Sofamor Danek USA Inc.
Medical DeviceApr 12, 2023
Philips Respironics Trilogy Evo O2 and LifeVentEVO2 Portable Electric Ventilator, Model recall — FDA Z-1287-2023
The accuracy of delivered oxygen may deviate below the required tolerance of 5% from setpoint when providing high concentration oxygen therapy. Additionally, if equipped, the internal FiO2…
Class IFDA: OngoingPhilips Respironics, Inc.
Medical DeviceApr 12, 2023
Stryker Color Cuff Non-Sterile Disposable Tourniquet Cuff -NS DISP 34X4,1BLA,2PRT QUICK recall — FDA Z-1342-2023
Not able to achieve desired pressure and not holding pressure result from two different causes which have been reported to occur during initial set-up of the cuff onto the patient, may lead…
Class IIFDA: OngoingStryker Corporation
Medical DeviceApr 12, 2023
Medtronic Accelerate Grafton DBF a) ACCELERATE BG SET T50203 GRAFTON DBF 3CC, REF T50203 recall — FDA Z-1332-2023
Potential for packaging non-conformances directly related to the dual-barrier, sterile pouch packaging system. Non-conforming packaging may lead to a breach in the sterile barrier.
Class IIFDA: OngoingMedtronic Sofamor Danek USA Inc.
How to use this monthly recall archive
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.