State

Alabama product recalls

73,722 recalls have nationwide distribution and so reach Alabama. 6,377 additional recalls listed Alabama specifically in their distribution scope.

What the numbers show

Total: 6,377
Critical: 1,129
Severe: 1,604
Most recent: 2026-10-28

Of the 6,377 recalls naming Alabama we have scored against our rubric, 1,129 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,604 (25%) are Severe.

Which agencies issued them

These figures cover only the 6,377 recalls whose distribution notice names Alabama specifically. The 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

28826–28850 of 80099

HighFDA (Devices)·Z-0613-2021·2020-12-23
Carl Zeiss Meditec VISULENS 550 Recalled for Electrical Shock Risk
Carl Zeiss Meditec is recalling VISULENS 550 refractive power measurement devices due to a defective communication board that may cause electrical shocks.
Product
Carl Zeiss Meditec Ag VISULENS 550 REF 2268-038 - Product Usage: is a device for measuring the refractive power of contact lenses and spectacle lenses and displaying measurement values for sphere, cylinder and prism.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0629-2021·2020-12-23
Biomet Recalls Sterile Trac System Thinflap Burr Hole Plates
Biomet is recalling specific lots of Sterile Trac System Thinflap 24 MM Burr Hole Plates because a breach in the sterile seal could lead to loss of sterility.
Product
Sterile Trac System Thinflap 24 MM Burr Hole Plate, Item number SP-STA-1021-12 - Product Usage: Fixation of Cranial bone
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0620-2021·2020-12-23
Biomet Shoulder System Surgical Handles Recalled for Sterile Seal Breach
Biomet is recalling specific lots of sterile shoulder system surgical instrument handles because a breach in the packaging seal could lead to loss of sterility.
Product
Comprehensive Total Shoulder System/Bio-Modular Choice Shoulder System, Item number 406669 - Product Usage: Surgical instrument handle, non-torque-limiting.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0621-2021·2020-12-23
Biomet Custom Cancellous Thread Recalled for Potential Sterile Seal Breach
Biomet is recalling specific lots of Custom Cancellous Thread devices because a breach in the sterile seal could lead to loss of sterility.
Product
Custom Cancellous Thread, Item numbers CP161941, CP161943 - Product Usage: 1. Noninflammatory degenerative joint disease including osteoarthritis and avascular necrosis. 2. Rheumatoid arthritis 3. Correction of functional deformity 4. Treatment of non-union, femoral neck…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0633-2021·2020-12-23
Maquet Cardiovascular Recalls HLS Set Advanced Due to Sterility Breach
Maquet Cardiovascular is recalling the HLS Set Advanced because of breaches in the product's sterility barrier. The device is used with the CARDIOHELP system for cardiac and pulmonary support.
Product
HLS Set Advanced, Model: BEQ-HLS 7050 USA; HLS Set Advanced 7.0 Product Code/Part Number: 70105.2794 - Product Usage: These devices are used with the CARDIOHELP system in order to provide extracorporeal circulation for cardiac support and/or pulmonary support.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0632-2021·2020-12-23
Maquet Cardiovascular Recalls HLS Set Advanced Due to Sterility Breaches
Maquet Cardiovascular is recalling HLS Set Advanced devices used for cardiac support due to breaches in the product's sterility barrier.
Product
HLS Set Advanced Model Name: BEQ-HLS 5050 USA; HLS Set Advanced 5.0, Product Code/Part Number: 70105.2797 - Product Usage: These devices are used with the CARDIOHELP system in order to provide extracorporeal circulation for cardiac support and/or pulmonary support.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0617-2021·2020-12-23
Biomet Cannulated Screw System Recalled for Potential Sterile Seal Breach
Biomet is recalling specific lots of cannulated screw systems because a breach in the sterile packaging seal could lead to loss of sterility.
Product
4.0/5.0mm Cannulated Screw System, BCS Cannulated Screw System (3.0, 4.0/5.0, 6.5/8.0mm), Item numbers 110009810, 110009821, 110009825, 110009852 - Product Usage: Fracture fixationof small bones, small bone fragements and long bones.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0628-2021·2020-12-23
Biomet Hip Prosthesis Recall for Potential Sterile Seal Breach
Biomet is recalling specific lots of RINGLOC BIPOLAR Hip System components due to a potential breach in the sterile seal, which could lead to loss of sterility.
Product
RINGLOC BIPOLAR Hip System Bi Polar Locking Ring, Item number 11-165304 - Product Usage: Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate, Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented, Prosthesis, Hip…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0588-2021·2020-12-23
BD PrecisionGlide Needles Recalled Due to Blood Contamination
Becton Dickinson is recalling BD PrecisionGlide needles because blood was found on the cannulas, posing a potential infection risk if not noticed by clinicians.
Product
BD PrecisionGlide Needle 30G x 1/2 (0.3 mm X 13mm) REF 305106 - Product Usage: used for general purpose injection and aspiration of fluids from vials, ampoules and parts of the body below the surface of the skin.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·20V810000·2020-12-23
International DuraStar and WorkStar Engine Control Software Defect Recall
Navistar recalls 17,213 2014-2021 International commercial trucks with an engine control defect. The software flaw can cause unexpected vehicle movement when parked with the PTO engaged, risking crashes and injury.
Product
INTERNATIONAL — INTERNATIONAL MV, DURASTAR, WORKSTAR, HV
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0636-2021·2020-12-23
Kowa VK-2s Software Recall for Potential Patient Data Deletion
Kowa Optimed Inc is recalling VK-2s software installed on nonmyd WX Retinal Cameras because a defect may cause the deletion of all patient information, potentially delaying treatment.
Product
Kowa VK-2s software Version 10.0.4.0, Product code 04987646809500 installed on Kowa nonmyd WX Retinal Cameras - Product Usage: is indicated for acquiring, displaying and storing image data from KOWA s mydriatic and non-mydriatic ophthalmic cameras.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·20V811000·2020-12-23
GM Recalls Bolt EV and Other Vehicles for Seat Belt Attachment Defect
General Motors is recalling multiple 2020-2021 vehicles due to incorrect bolts used to secure seat belts. Improperly fastened seat belts may fail to properly restrain occupants in a crash.
Product
CHEVROLET — CHEVROLET, CADILLAC, GMC SUBURBAN, ESCALADE NA, COLORADO, SILVERADO 3500
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0565-2021·2020-12-23
Terumo Capiox FX25 Advance Oxygenator Recall for Configuration Error
Terumo is recalling Capiox FX25 Advance Oxygenators because they may have the incorrect East or West configuration. The recall affects 5,079 units distributed in the US and abroad.
Product
(1) Capiox FX25 (West) Advance Oxygenator- with left port, 4-liter Reservoir, XC modified to Advance, Sterile Catalog Number: 3CX*FX25RWC (2) Capiox FX25 (East) Advance Oxygenator - FX25 with right port, 4-liter Reservoir, XC modified to Advance Catalog Number…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0152-2021·2020-12-23
Taro Recalls HEB Clotrimazole Cream Due to Impurity
Taro Pharmaceuticals is recalling HEB Clotrimazole Cream 1% because an unknown degradation impurity was detected slightly above the specification limit.
Product
HEB — HEB (CLOTRIMAZOLE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0634-2021·2020-12-23
Roche Recalls Tina-quant C-Reactive Protein Gen.3 Reagents Due to Cross-Contamination
Roche is recalling Tina-quant C-Reactive Protein Gen.3 reagents due to cross-contamination causing invalid calibrations and low quality control recovery.
Product
Tina-quant C-Reactive Protein Gen.3, Catalog number 05172373190 - Product Usage: the in vitro quantitative determination of CRP in human serum and plasma on Roche automated clinical chemistry analyzers.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0157-2021·2020-12-23
Taro Recalls Clotrimazole Cream Due to Unknown Degradation Impurity
Taro Pharmaceuticals is recalling Best Choice Clotrimazole Cream USP 1% because an unknown degradation impurity was detected slightly above the specification limit.
Product
Best Choice, Clotrimazole Cream, USP 1%, Antifungal, NET WT 0.5 OZ (14.2g), Distributed by: Valu Merchandisers, CO . 5000 Kansas Ave. Kansas City, KS 66106 Made in Canada. UPC 0-70038-20355-1
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0167-2021·2020-12-23
AvKARE Recalls Sildenafil Tablets Due to Packaging Mix-Up with Trazodone
AvKARE Inc. is recalling 38,715 bottles of Sildenafil 100 mg tablets because they were inadvertently packaged with trazodone at a third-party facility.
Product
Sildenafil Tablets USP 100 mg, Rx Only, 100-count Bottle, Manufactured for: AvKARE Pulaski, TN 38478, NDC 42291-748-01.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0156-2021·2020-12-23
Taro Recalls Rite Aid Clotrimazole Cream Due to Impurity
Taro Pharmaceuticals is recalling Rite Aid Clotrimazole Cream because an unknown degradation impurity was detected slightly above the specification limit.
Product
RiteAid Pharmacy RIngworm Cream, Clotrimazole Cream USP, 1%, Antifungal NET W 0.5 oz. (14.2g), Distributed by: Rite Aid, 30 Hunter Lane, Camp Hill, PA 17011 Made in Canada. UPC 0 11822 53812 1
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0155-2021·2020-12-23
Taro Recalls Kroger Clotrimazole Cream Due to Impurity
Taro Pharmaceuticals is recalling Kroger Clotrimazole Cream 1% because an unknown degradation impurity was detected slightly above the specification limit.
Product
KROGER — KROGER (CLOTRIMAZOLE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0635-2021·2020-12-23
Helena Laboratories Recalls K-ACT Actalyke Clotting Test Tubes
Helena Laboratories is recalling K-ACT Actalyke Clotting Test Tubes due to complaints of cracked or split caps.
Product
K-ACT Actalyke Clotting Test Tubes that are used in the: ACTALYKE XL ACTIVATED CLOTTING TIME ANALYZER, and ACTALYKE MINI ACTIVATED CLOTTING TIME TEST SYSTEM.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0169-2021·2020-12-23
Hikma Recalls Sodium Chloride Injection Vials Due to pH Failures
Hikma Pharmaceuticals is recalling 1.3 million vials of Sodium Chloride Injection USP 0.9% because pH test results were out of specification.
Product
SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0615-2021·2020-12-23
Medline Recalls RevMedX Trauma Dressings Due to Package Seal Integrity Issues
Medline Industries is recalling RevMedX Trauma Dressings because of package seal integrity issues. The recall affects 15,780 units distributed in the US and several international countries.
Product
RevMedX Trauma Dressings are packaged in a Tyvek Peel pouch, 1 Trauma Dressing per Tyvec Peel Pouch, 30 Pouches per Case; Sterile - Product Usage: are intended to absorb exudates.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0612-2021·2020-12-23
Medtronic Percept PC Neurostimulator Recall Due to Software Connection Failure
Medtronic is recalling 12 Percept PC Implantable Neurostimulators because a software anomaly in the A620 Patient Programmer prevents connection to the device.
Product
Percept PC Implantable Neurostimulator (INS) - Product Usage: The Percept PC is a neurostimulation device for deep brain stimulation therapy. It is indicated for DBS treatment for Parkinson s disease, essential tremor, dystonia, obsessive-compulsive disorder, and epilepsy.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0180-2021·2020-12-23
Fusion Health Recalls Pharmorigins Core Supplement for Unapproved Additive
Fusion Health and Vitality LLC is recalling Pharmorigins Core dietary supplements due to the unapproved use of a food additive and unapproved marketing statements.
Product
PHARMORIGINS CORE with Natural Orange Flavor NATURAL ENERGY and IMMUNE HEALTH Dietary Supplement 30 Servings (45g) Supplement Facts***Hordenine HCL*** Manufactured by: Fusion Health Vitality, LLC 1360 Union Hill Road, Suite 11B Alpharetta, GA 30004 888.964.5327 UPC 7 28028 21054…
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0159-2021·2020-12-23
Taro Recalls Clotrimazole Cream Due to Unknown Degradation Impurity
Taro Pharmaceuticals is recalling specific lots of Clotrimazole Cream USP 1% because an unknown degradation impurity was detected slightly above the specification limit.
Product
Athlete's Foot Cream, Clotrimazole Cream USP, 1%, Antifungal Cream, NET WT 1 oz (30 g), Distributed by: Taro Pharmaceuticals U.S.A. Inc. Hawthorne, NY 10531. Made in Canada. UPC 3 51672 20022 0
Category
Drug
Distribution
Distributed nationwide