State

Alabama product recalls

73,824 recalls have nationwide distribution and so reach Alabama. 6,378 additional recalls listed Alabama specifically in their distribution scope.

What the numbers show

Total: 6,378
Critical: 1,129
Severe: 1,605
Most recent: 2026-11-04

Of the 6,378 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 1,605 (25%) are Severe.

Which agencies issued them

These figures cover only the 6,378 recalls whose distribution notice names Alabama specifically. The 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

48726–48750 of 80202

SevereFDA (Devices)·Z-1133-2017·2017-02-08
Medtronic Intact Disposable Wands Recalled for Sterility Compromise
Medtronic is recalling Intact Disposable Wands because the sterile barrier was breached, compromising sterility. The recall covers 275 units distributed worldwide.
Product
Intact Disposable Wands (part of the Intact System) 900-120: 5 Pack 20mm Disposable Product Usage: The Intact Medical disposable wands are intended to provide breast tissue for histologic examination with partial or complete removal of an imaged abnormality and to provide…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0459-2017·2017-02-08
VistaPharm Recalls Metoclopramide Oral Solution Due to Potential Water Contamination
VistaPharm is recalling specific lots of Metoclopramide Oral Solution because the purified water used in manufacturing may have been contaminated with Burkholderia cepacia.
Product
Metoclopramide Oral Solution, USP 10 mg/ 10 mL, 50 unit dose cups of 10 mL per case, Rx only, Manufactured by VistaPharm, Largo, FL 33771, NDC No. 66689-031-50.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1108-2017·2017-02-08
PerkinElmer Spare Disk Remover Module Recall Due to Corrosion Risk
PerkinElmer is recalling Spare Disk Remover Modules because defective axles may corrode in humid conditions, potentially contaminating test plates.
Product
Spare Disk Remover Module; Product Number: 61001820 Intended for in vitro quantitative and qualitative determination of analytes in body fluids.
Category
Medical Device
Distribution
4 states
HighNHTSA·17V080000·2017-02-08
Mercedes-Benz Recalls 2017 Models for Air Bag Ignition Failure
Mercedes-Benz is recalling 2017 E300, E400, E550, GLA 250, and CLA250 vehicles because the pelvis or front passenger air bag inflator may fail to ignite in a crash.
Product
MERCEDES-BENZ — MERCEDES-BENZ E300, E400, GLA 250, CLA250
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1107-2017·2017-02-08
PerkinElmer Genetic Screening Processor Recalled for Corroding Axles
PerkinElmer is recalling 24 Genetic Screening Processor instruments because defective ball bushing axles may corrode in humid conditions, risking contamination of sample wells.
Product
Genetic Screening Processor (GSP); PerkinElmer Part Number= 2021-0010 Intended for in vitro quantitative and qualitative determination of analytes in body fluids.
Category
Medical Device
Distribution
4 states
HighFDA (Devices)·Z-1122-2017·2017-02-08
Mevion S250 Proton Therapy Units Recalled for Data Loss Error
Mevion Medical Systems is recalling two S250 Proton Radiation Therapy units because a software error can cause Delta corrections to be lost.
Product
MEVION S250-Proton Radiation Therapy Product Usage: Proton Radiation Therapy
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1364-2017·2017-02-08
Rich Products Recalls Ice Cream Layer Cakes Due to Undeclared Walnuts
Rich Products Corp. is recalling specific Jon Donaire Ice Cream Layer Cakes because they may contain undeclared walnuts from a supplier.
Product
Jon Donaire Ice Cream Layer Cake, Deliciously moist white cake with rich, creamy vanilla ice cream, NET WT 4 LB 8 OZ, KEEP FROZEN, UPC 0 49800 62878 6 (retail), Product Code 62878, and UPC 0 49800 02453 3 (retail), Product Code 02453 --- Rich Products Corp., Buffalo, NY 14213…
Category
Food
Distribution
35 states
HighFDA (Devices)·Z-1128-2017·2017-02-08
Medtronic Intact Disposable Wands Recalled for Sterility Compromise
Medtronic is recalling Intact Disposable Wands because the sterile barrier was breached, compromising sterility. The recall affects 180 units distributed worldwide.
Product
Intact Disposable Wands (part of the Intact System) 777-112: 5 Pack 12mm Disposable Product Usage: The Intact Medical disposable wands are intended to provide breast tissue for histologic examination with partial or complete removal of an imaged abnormality and to provide…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1127-2017·2017-02-08
Medtronic Intact Disposable Wands Recalled Due to Sterility Compromise
Medtronic is recalling Intact Disposable Wands because the sterile barrier was breached, compromising sterility. The recall covers 155 units distributed worldwide.
Product
Intact Disposable Wands (part of the Intact System) 900-112: 5 Pack 12mm Disposable Product Usage: The Intact Medical disposable wands are intended to provide breast tissue for histologic examination with partial or complete removal of an imaged abnormality and to provide…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·17V075000·2017-02-08
Volkswagen Recalls 2017 Passat Vehicles Due to Brake Fluid Leak Risk
Volkswagen is recalling 2017 Passat vehicles because brake fluid may leak from line connections, potentially increasing stopping distance and crash risk.
Product
VOLKSWAGEN — VOLKSWAGEN PASSAT
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1124-2017·2017-02-08
Synthes Radial Head Prosthesis Recalled for Potential Stem Loosening
Synthes (USA) Products LLC is recalling 50,311 units of the Radial Head Prosthesis System because the radial stem may loosen post-operatively at the stem bone interface.
Product
Synthes Radial Head Prosthesis System, Surgical instrument motors and accessories Product Usage: Intended for primary and revision joint replacement of the radial head.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1135-2017·2017-02-08
Medtronic Intact Disposable Wands Recalled for Sterility Compromise
Medtronic is recalling Intact Disposable Wands because the sterile barrier was breached, compromising product sterility.
Product
Intact Disposable Wands (part of the Intact System) 777-120BT: 5 Pack 20mm Disposable Product Usage: The Intact Medical disposable wands are intended to provide breast tissue for histologic examination with partial or complete removal of an imaged abnormality and to provide…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1111-2017·2017-02-08
Organ Preservation Solution Recalled for Potential Bacterial Contamination
Organ Recovery Systems is recalling SPS-1 Static Preservation Solution bags due to potential bacterial contamination.
Product
SPS-1, Static Preservation Solution [1 or 2 liter bags], Sterile; Organ Recovery Systems, One Pierce Place, Itasca, IL 60143
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0450-2017·2017-02-08
Dr. Reddy's Recalls Flucanazole Tablets for Dissolution Failures
Dr. Reddy's is recalling Flucanazole tablets that failed dissolution and stability specifications. Patients should stop using the affected lots and consult their healthcare provider.
Product
FLUCONAZOLE — FLUCONAZOLE (FLUCONAZOLE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1121-2017·2017-02-08
Medtronic Strata II Valves Recalled for Pressure Discrepancies
Medtronic is recalling Strata II and Strata NSC valves used for hydrocephalus management due to reported discrepancies between the set pressure level and x-ray readings.
Product
Medtronic Strata II / Strata NSC Valves (includes Burr Hole and Lumbar Peritoneal. All Catalog Numbers. Strata-type valves are used in the management of hydrocephalus. The Strata II/Strata NSC valve is a shunt component designed to allow for continuous flow of cerebrospinal…
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·17083·2017-02-08
La-Z-Boy Recalls Lift Chair Power Supplies Due to Shock Hazard
La-Z-Boy is recalling specific power supplies sold with lift chairs because the covers can crack and detach, exposing electrical components and posing a shock hazard.
Product
Power supplies sold with lift chairs
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1120-2017·2017-02-08
Siemens IMMULITE PSA Kit Recall Due to Negative Bias Results
Siemens is recalling two lots of IMMULITE PSA kits because they produce negative bias results, potentially affecting prostate cancer screening accuracy.
Product
IMMULITE/IMMULITE 1000 Systems, Third Generation PSA, Catalog Number/REF LK3PS1, SMN 10706293 (US Kit Catalog) Product Usage: For in vitro diagnostic use with the IMMULITE¿ and IMMULITE 1000 Analyzers for the quantitative measurement of prostate-specific antigen (PSA) in…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1363-2017·2017-02-08
Rich Products Recalls Ice Cream Layer Cakes Due to Undeclared Walnuts
Rich Products Corp is recalling Jon Donaire Ice Cream Layer Cakes because they may contain undeclared walnuts from a supplier.
Product
Jon Donaire Ice Cream Layer Cake, Deliciously moist white cake with rich, creamy strawberries & cream ice cream, NET WT 4 LB 8 OZ, KEEP FROZEN, UPC 0 49800 04776 1 (retail), Product Code 04776 --- Rich Products Corp., Buffalo, NY 14213
Category
Food
Distribution
35 states
HighFDA (Devices)·Z-1125-2017·2017-02-08
Covidien Nellcor SpO2 Forehead Sensor Recalled for Latex Labeling Error
FDA is recalling 7,453 units of the Covidien Nellcor SpO2 Forehead Sensor because the label incorrectly states the product is latex-free, while the headband contains latex.
Product
Covidien Nellcor SpO2 Forehead Sensor Item Code: RS10; The Covidien Nellcor¿ Forehead SpO2Sensor, model RS10, is indicated for use when continuous non-invasive arterial oxygen saturation and pulse rate monitoring are required for patients weighing more than 40 kg.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1129-2017·2017-02-08
Medtronic Intact Disposable Wands Recalled for Sterility Compromise
Medtronic is recalling 252 Intact Disposable Wands because the sterile barrier was breached, compromising sterility. The devices are used for breast tissue removal.
Product
Intact Disposable Wands (part of the Intact System) 777-112BT: 5 Pack 12mm Disposable Product Usage: The Intact Medical disposable wands are intended to provide breast tissue for histologic examination with partial or complete removal of an imaged abnormality and to provide…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0465-2017·2017-02-08
VistaPharm Recalls Methadone Hydrochloride Due to Potential Bacterial Contamination
VistaPharm is recalling Methadone Hydrochloride Oral Concentrate because purified water used in manufacturing may have been contaminated with Burkholderia cepacia.
Product
METHADONE HYDROCHLORIDE — METHADONE HYDROCHLORIDE (METHADONE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·17V078000·2017-02-08
Mercedes-Benz Recalls 2017 E300 Models Due to Shift Lever Module Defect
Mercedes-Benz is recalling 2017 E300 and E300 4Matic vehicles because a damaged shift lever module may prevent gear selection, increasing crash risk.
Product
MERCEDES-BENZ — MERCEDES-BENZ E300
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1134-2017·2017-02-08
Medtronic Intact Disposable Wands Recalled for Sterility Compromise
Medtronic is recalling 326 Intact Disposable Wands because the sterile barrier was breached, compromising sterility. The recall covers units distributed in the US and several international countries.
Product
Intact Disposable Wands (part of the Intact System) 777-120: 5 Pack 20mm Disposable Product Usage: The Intact Medical disposable wands are intended to provide breast tissue for histologic examination with partial or complete removal of an imaged abnormality and to provide…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1366-2017·2017-02-08
Rich's White Cake with Vanilla Ice Cream Recalled for Undeclared Walnuts
Rich Products Corp is recalling specific lots of Rich's 1/4 Sheet White Cake with Vanilla Ice Cream because the product may contain undeclared walnuts.
Product
RICH'S 1/4 Sheet White Cake with Vanilla Ice Cream Cake, KEEP FROZEN, UNIT NET WT: 60 OZ (3 LB 12 OZ), COUNT: 4 x 1/4 SHEET CAKES, NET CASE WT: 15 LB, UPC 049800 290013 (retail), Product Code 29001 --- RICH PRODUCTS CORP BUFFALO, NY 14213
Category
Food
Distribution
35 states
HighFDA (Devices)·Z-1119-2017·2017-02-08
Siemens Recalls IMMULITE PSA Kits Due to Negative Bias
Siemens Healthcare Diagnostics is recalling IMMULITE PSA kits worldwide because patient samples show an average negative bias of approximately -22%.
Product
IMMULITE/IMMULITE 1000 Systems, Third Generation PSA, Catalog Number/REF LKUP1, SMN 10380956 (OUS Kit Catalog) Product Usage: For in vitro diagnostic use with the IMMULITE¿ and IMMULITE 1000 Analyzers for the quantitative measurement of prostate-specific antigen (PSA) in…
Category
Medical Device
Distribution
Distributed nationwide