FoodDec 15, 2021
Oregon Lox Company North Coast Traditional Nova Lox, cold smoked salmon, various recall — FDA F-0244-2022
Listeria monocytogenes.
Class IFDA: TerminatedOregon Lox Company
Latest records
Latest recalls — page 791
The newest recall records with useful source details are listed here.
FoodDec 15, 2021
Gerber Products Company dba Nestle Infant 6.6 oz recall — FDA F-0271-2022
Beetles were found in the pea ingredient used in the side compartment of the tray.
Class IIIFDA: TerminatedGerber Products Company dba Nestle Infant Nutrition
FoodDec 15, 2021
Cargill Cocoa & Chocolate Wilbur Dark Chocolate Triple Covered Malted Milk Balls recall — FDA F-0274-2022
Product recalled because of the presence of undeclared peanuts.
Class IFDA: TerminatedCargill Cocoa & Chocolate, Inc.
DrugDec 15, 2021
Fexofenadine HCl, 60 mg & Pseudoephedrine HCl 120 mg, Extended Release Tablets USP, Allergy recall — FDA D-0275-2022
Failed dissolution specifications
Class IIIFDA: TerminatedDr. Reddy's Laboratories, Inc.
DrugDec 15, 2021
American Screening AmericanScreening HAND SANITIZER (ethyl alcohol 70%) ANTIMICROBIAL recall — FDA D-0266-2022
Labeling Not Elsewhere Classified: Hand sanitizer packaged in containers resembling drinking water bottles.
Class IFDA: CompletedAmerican Screening LLC
DrugDec 15, 2021
Apollo Care VANComycin 1g added to 250mL of 0.9% Sodium Chloride recall — FDA D-0277-2022
Crystallization: Product appears to be turbid.
Class IIFDA: TerminatedApollo Care
DrugDec 15, 2021
Dr. Reddy's Laboratories Antihistamine & Nasal Decongestant, Fexofenadine HCl 60 mg and recall — FDA D-0270-2022
Failed dissolution specifications
Class IIIFDA: TerminatedDr. Reddy's Laboratories, Inc.
DrugDec 15, 2021
Dr. Reddy's Laboratories Antihistamine & Nasal Decongestant, Fexofenadine HCl 60 mg and recall — FDA D-0271-2022
Failed dissolution specifications
Class IIIFDA: TerminatedDr. Reddy's Laboratories, Inc.
VehicleDec 13, 2021
Toyota 4Runner headlights recall — NHTSA campaign 21V963000
Southeast Toyota Distributors, LLC (SET) is recalling certain 2022 Toyota 4Runner vehicles. The driver's side high beam may be inoperable after the installation of accessory fog lights. As…
headlightsSoutheast Toyota Distributors, LLC
VehicleDec 9, 2021
Frontier critical fasteners recall — NHTSA campaign 21V958000
Nissan North America, Inc. (Nissan) is recalling certain 2022 Frontier vehicles. The seat belt bracket mounting bolts on the left-rear seat may have been incorrectly tightened. As such,…
critical fastenersNissan North America, Inc.
VehicleDec 9, 2021
Rogue fuel pump recall — NHTSA campaign 21V957000
Nissan North America, Inc. (Nissan) is recalling certain 2021 Rogue vehicles. Abnormal wear inside the fuel pump may cause it to overheat and fail.
fuel pumpNissan North America, Inc.
VehicleDec 9, 2021
Ascent tie rod recall — NHTSA campaign 21V954000
Subaru of America, Inc. (Subaru) is recalling certain 2020 Ascent vehicles. Due to an incorrect tapered hole in the housing, the front tie rod ends may not fit properly. The improper fit…
tie rodSubaru of America, Inc.
VehicleDec 9, 2021
Jeep Grand Cherokee L lighting control module software recall — NHTSA campaign 21V950000
Chrysler (FCA US, LLC) is recalling certain 2021 Jeep Grand Cherokee L vehicles equipped with smart lighting modules (SLM). An incomplete SLM software update may cause one or both…
lighting control module softwareChrysler (FCA US, LLC)
VehicleDec 9, 2021
Subaru of control module (tcm/pcm/tecm) recall — NHTSA campaign 21V955000
Subaru of America, Inc. (Subaru) is recalling certain 2019-2020 Ascent, 2020 Legacy and Outback vehicles. A programming error in the Transmission Control Unit (TCU) may allow the clutch to…
control module (tcm/pcm/tecm)Subaru of America, Inc.
Medical DeviceDec 8, 2021
Cardiac Assist SHIP KIT, PROCEDURE KIT, PROTEKDUO LS - DL31 for temporary Cardiopulmonary recall — FDA Z-0311-2022
Top label of the outer package of the collection kit Item 5820-3118 showed expiration date of 2022/05/01 (correct expiration date) while side label showed expiration date of 2021/05/01…
Class IIIFDA: OngoingCardiac Assist, Inc.
Medical DeviceDec 8, 2021
GE Healthcare GE Centricity Universal Viewer Zero Footprint Client recall — FDA Z-0329-2022
There is a potential to display incomplete patient imaging study.
Class IIFDA: TerminatedGE Healthcare, LLC
Medical DeviceDec 8, 2021
NUVASIVE PRECICE Intramedullary Limb Lengthening (IMLL) and (Short) System: Model recall — FDA Z-0319-2022
The Instructions for Use have been updated to include: (1) Clarification that the device is intended for use only in patients 18 years and older, (2) That patients should weigh 50 lbs. or…
Class IIFDA: OngoingNuVasive Specialized Orthopedics, Inc.
Medical DeviceDec 8, 2021
Thoratec Abbott HeartMate Touch Communication System, REF: HMT1100 (US), HMT1100-R recall — FDA Z-0308-2022
If LVAS communication system is trying to establish Bluetooth connection and another Bluetooth-enabled device is nearby and advertising for Bluetooth connection, the Bluetooth connectivity…
Class IIFDA: OngoingThoratec Corp.
Medical DeviceDec 8, 2021
Boston Scientific HURRICANE RX DILATION BALLOON 8MM 4CM -for endoscopic dilatation of recall — FDA Z-0325-2022
Balloon pinhole results in losss pressure or fails to gain or maintain pressure, causing prolonged procedure
Class IIFDA: OngoingBoston Scientific Corporation
Medical DeviceDec 8, 2021
Boston Scientific HURRICANE RX DILATION BALLOON 8MM 2CM -for endoscopic dilatation of recall — FDA Z-0324-2022
Balloon pinhole results in losss pressure or fails to gain or maintain pressure, causing prolonged procedure
Class IIFDA: OngoingBoston Scientific Corporation
Medical DeviceDec 8, 2021
Magnolia Medical Technologies The Steripath Gen2 Blood Collection System Model recall — FDA Z-0318-2022
Due to an uptick of complaints associated with premature needle retraction of blood collection system.
Class IIFDA: TerminatedMagnolia Medical Technologies, Inc.
Medical DeviceDec 8, 2021
O&M HALYARD HALYARD STERLING ZERO NITRILE POWDER-FREE EXAM GLOVES, Sizes XS, S, M, L, and XL recall — FDA Z-0317-2022
All lots of the glove may discolor and lose elasticity upon aging, resulting in the inability of the user to don the gloves without tearing.
Class IIFDA: OngoingO&M HALYARD Inc.
Medical DeviceDec 8, 2021
BioFire Blood Culture Identification 2 (BCID2) Panel Part No: RFIT-ASY-0147 UDI recall — FDA Z-0312-2022
Due to an increased risk of false positive Acinetobacter calcoaceticus- baumannii complex results. The cause may be as a due to non-viable contamination in the blood culture vials.
Class IIFDA: TerminatedBioFire Diagnostics, LLC
Medical DeviceDec 8, 2021
RANDOX CHOL-cholesterol (total) test system intended to measure cholesterol in plasma and recall — FDA Z-0328-2022
When calibrating using the standard provided in the kit, the change in absorbance is lower than expected generating internal quality control results high outside range
Class IIFDA: TerminatedRandox Laboratories Ltd.
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Recent recall archives
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