FoodSep 13, 2023
PBM Nutritionals Parent's Choice brand Sensitivity Premium Infant Formula recall — FDA F-1493-2023
Inadvertent release of rejected product to market
Class IIIFDA: TerminatedPBM Nutritionals, LLC
Latest records
Latest recalls — page 508
The newest recall records with useful source details are listed here.
FoodSep 13, 2023
Cooperstown Cheese Company 1 recall — FDA F-1490-2023
Cheese may be contaminated with Listeria monocytogenes.
Class IIFDA: TerminatedCooperstown Cheese Company, LLC
DrugSep 13, 2023
Fosfomycin Tromethamine Granules for Oral Solution, 3 g single- dose sachet recall — FDA D-1145-2023
Failed Impurities/Degradation Specifications: Out-of-specification results observed for the organic impurities test at 6 months, RT Stability.
Class IIIFDA: TerminatedAscend Laboratories, LLC
DrugSep 13, 2023
Marlex Pharmaceuticals Digoxin Tablets, USP 0.125mg, 100-count bottles recall — FDA D-1169-2023
Labeling: Label Mix-Up- Bottles labeled as Digoxin Tablets, USP 0.125 mg contain Digoxin Tablets, USP 0.25mg and bottles labeled as Digoxin Tablets, USP 0.25mg contain Digoxin Tablets, USP…
Class IFDA: TerminatedMarlex Pharmaceuticals, Inc.
DrugSep 13, 2023
Marlex Pharmaceuticals Digoxin Tablets, USP 0.25mg, 100-count bottles recall — FDA D-1170-2023
Labeling: Label Mix-Up- Bottles labeled as Digoxin Tablets, USP 0.125 mg contain Digoxin Tablets, USP 0.25mg and bottles labeled as Digoxin Tablets, USP 0.25mg contain Digoxin Tablets, USP…
Class IIFDA: TerminatedMarlex Pharmaceuticals, Inc.
DrugSep 13, 2023
Sodium Fluoride 1.1%, SODIUM FLUORIDE Prescription Dental Toothpaste, 5000 ppm Fluoride Plus recall — FDA D-1146-2023
Cases of Sodium Fluoride 1.1% Prescription Dental Toothpaste may contain cartons labeled as Capsaicin Cream 0.025% but contain correctly labeled tubes of Sodium Fluoride 1.1% Prescription…
Class IIFDA: TerminatedAVKARE LLC
DrugSep 13, 2023
Capsaicin Cream 0.025%, External Analgesic Cream, Penetrating Pain Relief, NET WT. 2.1 OZ. recall — FDA D-1147-2023
Product mix-up: Cartons labeled Capsaicin Cream 0.025% may contain tubes of Sodium Fluoride 1.1% Prescription Dental Toothpaste
Class IIFDA: TerminatedAVKARE LLC
DrugSep 13, 2023
Milrinone Lactate Injection, USP 20mg/20 mL (1mg/mL) recall — FDA D-1144-2023
Failed Impurities/Degradation Specifications
Class IIIFDA: TerminatedCaplin Steriles Limited
VehicleSep 8, 2023
Ford traction battery recall — NHTSA campaign 23V626000
Ford Motor Company (Ford) is recalling certain 2020-2022 Lincoln Aviator and Ford Explorer vehicles equipped with 3.0L PHEV engines. A manufacturing defect in one or more of the high…
traction batteryFord Motor Company
VehicleSep 8, 2023
Nissan camera recall — NHTSA campaign 23V628000
Nissan North America, Inc. (Nissan) is recalling certain 2019-2021 Altima and 2020-2021 Sentra vehicles. Damage to the camera harness can cause distortion or loss of the rearview camera…
cameraNissan North America, Inc.
Medical DeviceSep 6, 2023
Datascope Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP), Part Numbers 0998-00-0800-31 recall — FDA Z-2486-2023
Users were experiencing a failure in the IAB Fiber Optic Sensor input on the IABP when inserting the Intra-Aortic Balloon Fiber Optic connector.
Class IIFDA: OngoingDatascope Corp.
Medical DeviceSep 6, 2023
RAYSEARCH LABORATORIES AB RayCare software, include version number 5A, 5B, 6A, including recall — FDA Z-2464-2023
An issue was found in Software RayCare 5A, 5B, 6A, including service packs, where an allergy warning against medication substance (drug ingredient) will not be displayed as expected under…
Class IIFDA: OngoingRAYSEARCH LABORATORIES AB
Medical DeviceSep 6, 2023
Siemens Healthcare Diagnostics epoc BGEM BUN Test Card with epoc Host SW v3.37.3, epoc NXS recall — FDA Z-2476-2023
There is potential for discrepant high glucose results in samples with glucose results on the lower end of the reportable range.
Class IIFDA: OngoingSiemens Healthcare Diagnostics Inc.
Medical DeviceSep 6, 2023
Accuray Upper roller bracket (part number 1088370) for the Gen2 gantry enclosure for the recall — FDA Z-2489-2023
It is possible the upper roller bracket in the Radixact System gantry enclosure may not provide enough clearance for service personnel to use a jib crane for moving components while…
Class IIFDA: CompletedAccuray Inc.
Medical DeviceSep 6, 2023
Oculus Pentacam AXL Wave, Ref 70020, CE 0123 recall — FDA Z-2482-2023
Their is a potential that optical devices with insufficient anti-reflective coating may lead to incorrect axial length measurements.
Class IIFDA: OngoingOculus Optikgeraete GMBH
Medical DeviceSep 6, 2023
Datascope Cardiosave Rescue Intra-Aortic Balloon Pumps (IABP), Part Numbers 0998-00-0800-75 recall — FDA Z-2436-2023
Users were reporting instances of "Gas Loss in IAB Circuit" and "Gas Gain in IAB Circuit" alarms while providing therapy. An internal investigation of the complaints determined that there…
Class IFDA: OngoingDatascope Corp.
Medical DeviceSep 6, 2023
Siemens Healthcare Diagnostics epoc BGEM Test Card (BUN & TCO2),Veterinary with epoc Host SW recall — FDA Z-2478-2023
There is potential for discrepant high glucose results in samples with glucose results on the lower end of the reportable range.
Class IIFDA: OngoingSiemens Healthcare Diagnostics Inc.
Medical DeviceSep 6, 2023
Beckman Coulter, IVD, REF: OSR61171, IgA, 4 x 14 mL R1, 4 x 11 mL R2 recall — FDA Z-2488-2023
Lipemic interference failed to meet the performance specification listed within the IFU.
Class IIFDA: OngoingBeckman Coulter Inc.
Medical DeviceSep 6, 2023
Skytron GS70 Salus Surgical Table, Product Code 18-070-70 recall — FDA Z-2469-2023
When the control of the operating table was used in Bluetooth mode, the operating table continued moving even after releasing the button on the control. Originally, the root cause was…
Class IIFDA: OngoingSkytron, LLC
Medical DeviceSep 6, 2023
LeMaitre Vascular The Chevalier Valvulotome is a device used to disrupt the valves of veins recall — FDA Z-2468-2023
Burrs (molding flash) on the cutter may tear the harvested vien
Class IIFDA: OngoingLeMaitre Vascular, Inc.
Medical DeviceSep 6, 2023
Siemens Healthcare Diagnostics Atellica CH Triglycerides_2: in vitro diagnostic use in the recall — FDA Z-1271-2023
Reagent Carryover from LDL Cholesterol Direct (DLDL), Total Protein II (TP), Triglycerides (Trig), and Triglycerides_2 (Trig_2) Impacting Magnesium (Mg) Results
Class IIFDA: OngoingSiemens Healthcare Diagnostics, Inc.
Medical DeviceSep 6, 2023
Reichert PHOROPTOR VRX DIGITAL REFRACTION SYSTEM-Digital refractor intended for the recall — FDA Z-2512-2023
Phoroptor VRx Head may detach from the bracket that connects the Phoroptor VRx Head to an ophthalmic stand. If the Phoroptor VRx Head detaches from the bracket, it can fall onto a patient…
Class IIFDA: OngoingReichert, Inc.
Medical DeviceSep 6, 2023
Siemens Healthcare Diagnostics Atellica CH LDL Cholesterol- In vitro diagnostic use in the recall — FDA Z-2472-2023
Potential for reagent carryover on the Atellica CH 930 resulting in a positive bias that could impact quality control (QC), patient samples, and calibrator results with from Atellica CH…
Class IIFDA: OngoingSiemens Healthcare Diagnostics, Inc.
Medical DeviceSep 6, 2023
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V Wireless Foot Switch distributed with Philips Allura recall — FDA Z-2485-2023
Loss of availability of the wireless foot switch during procedures.
Class IIFDA: OngoingPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
September 2026364 records · 4 categoriesAugust 2026302 records · 4 categoriesJuly 2026370 records · 4 categoriesJune 2026376 records · 4 categoriesMay 2026340 records · 4 categoriesApril 2026415 records · 4 categoriesMarch 2026190 records · 4 categoriesFebruary 2026331 records · 4 categoriesJanuary 2026212 records · 4 categoriesDecember 2025389 records · 4 categoriesNovember 2025326 records · 4 categoriesOctober 2025455 records · 4 categories