State

Alabama product recalls

73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

33526–33550 of 80114

SevereFDA (Drugs)·D-0524-2020·2019-12-04
AVKARE Recalls Ranitidine Tablets Due to NDMA Impurity
AVKARE Inc. is recalling specific lots of Ranitidine Tablets 150 mg because the active ingredient contained the impurity N-nitrosodimethylamine (NDMA).
Product
AVKARE Ranitidine Tablets, USP 150 mg Rx Only Manufactured for: AvKARE, Inc. Pulaski, TN 38478 Manufactured by: Amneal Pharmaceuticals of NY Hauppauge, NY 11788 a) 1000 tablets NDC 42291-724-10; b) 180 tablets NDC 42291-724-18; c) 60 tablets NDC 42291-724-60
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0526-2020·2019-12-04
AuroMedics Recalls Ranitidine Tablets Due to NDMA Detection
AuroMedics Pharma LLC is recalling DG Health Acid Reducer Ranitidine Tablets 150 mg because N-nitrosodimethylamine (NDMA) was detected in the product.
Product
DG Health Acid Reducer Ranitidine Tablets 150 mg, 8-count carton, Distributed by: Dolgencorp LLC 100 Mission Ridge Goodletville TN 37072 NDC 55910-092-79
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0529-2020·2019-12-04
AuroMedics Recalls Ranitidine Syrup Due to NDMA Contamination
AuroMedics Pharma LLC is recalling Ranitidine Syrup because N-nitrosodimethylamine (NDMA) has been detected in the product.
Product
Ranitidine Syrup (Ranitidine Oral Solution, USP), 15 mg/mL (75 mg/5mL) 474 mL bottle, Rx only Distributed by: Aurobindo Pharma USA Inc. 279 Princeton-Hightstown Road East Windsor, NJ 08520 Made in India NDC 65862-431-74
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0573-2020·2019-12-04
AuroMedics Recalls MARLIDO KIT Vials Due to Foreign Material Presence
AuroMedics Pharma LLC is recalling MARLIDO KIT vials because foreign material was found inside the vials. The affected product is Lidocaine HCl Injection, USP, 2%.
Product
MARLIDO KIT — MARLIDO KIT (MARCAINE, LIDOCAINE, POVIDONE IODINE)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·19V860000·2019-12-04
REV Recalls Fleetwood and Holiday Rambler Motorhomes Due to Exhaust Defect
REV Recreation Group is recalling 3,241 Fleetwood and Holiday Rambler motorhomes because the generator exhaust pipe placement may allow carbon monoxide to enter the vehicle.
Product
HOLIDAY RAMBLER — HOLIDAY RAMBLER, FLEETWOOD VACATIONER, BOUNDER, SOUTHWIND
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0521-2020·2019-12-04
Zimmer Biomet Recalls Acromium Flange Sets Due to Cleaning Issues
Zimmer Biomet is recalling Acromium Flange Sets because elevated levels of bacterial endotoxin and residual debris remain on the devices due to a cleaning issue.
Product
ACROMIUM FLANGE SET (Custom product) Item No. PM555148 - Product Usage: Arcomium replacement.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0530-2020·2019-12-04
Aurobindo Ranitidine Capsules Recalled for NDMA Contamination
AuroMedics Pharma LLC is recalling Aurobindo Ranitidine Capsules 150 mg because N-nitrosodimethylamine (NDMA) was detected in the product.
Product
Aurobindo Ranitidine Capsules 150 mg, 500 count bottle, Rx Only Distributed by: Aurobindo Pharma USA, Inc. 279 Princeton-Hightstown Road East Windsor, NJ 08520 NDC 59651-144-05
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·19V859000·2019-12-04
Ford Recalls 2020 Explorer and Lincoln Aviator for Fuel Leak Risk
Ford is recalling 2020 Explorer and Lincoln Aviator vehicles because a chafing fuel line may cause a leak, increasing the risk of fire.
Product
FORD — FORD, LINCOLN EXPLORER, AVIATOR
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0527-2020·2019-12-04
Aurobindo Ranitidine Capsules Recalled for NDMA Contamination
AuroMedics Pharma LLC is recalling Aurobindo Ranitidine Capsules 150 mg because N-nitrosodimethylamine (NDMA) was detected in the product.
Product
Aurobindo Ranitidine Caspules 150 mg, 60-count bottle, Rx Only Distributed by: Aurobindo Pharma USA, Inc. 279 Princeton-Hightstown Road East Windsor, NJ 08520 NDC 59651-144-60
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·19V862000·2019-12-04
Volkswagen Recalls Diesel Vehicles for Air Bag Inflator Defect
Volkswagen is recalling certain 2011-2015 Golf, Passat, and Audi A3 diesel vehicles because the driver's side air bag inflator may explode.
Product
VOLKSWAGEN — VOLKSWAGEN, AUDI GOLF, A3, PASSAT
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·19V863000·2019-12-04
Bentley Recalls 2017-2018 Continental Supersports for Steering Fluid Leak Risk
Bentley is recalling 2017-2018 Continental Supersports vehicles because a power steering cooler pipe may be the incorrect size, allowing the hose to detach and leak fluid.
Product
BENTLEY — BENTLEY CONTINENTAL
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0519-2020·2019-12-04
Zimmer Biomet Recalls Compress Mini Compress Devices Due to Cleaning Issues
Zimmer Biomet is recalling Compress Mini Compress devices because elevated bacterial endotoxin and residual debris remain on the devices due to a cleaning issue.
Product
Compress, Mini Compress; Item Nos. 178350 178351 178352 178353 178354 178355 178356 178357 178358 178359 178360 178361 178362 178363 178364 178365 178366 178367 178368 178369 178370 178371 178372 178373 178464 178472 178480 178488 178496 178504…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0581-2020·2019-12-04
Siemens Atellica CH 930 Analyzer Recalled for Calibration Error
Siemens Healthcare Diagnostics is recalling 1,432 Atellica CH 930 Analyzers due to a potential calibration error that may cause results to be five times higher than expected.
Product
Atellica CH 930 Analyzer
Category
Medical Device
Distribution
35 states
HighNHTSA·19V861000·2019-12-04
Fleetwood and Holiday Rambler Motorhomes Recalled for Fire Risk
REV is recalling 2020 Fleetwood and Holiday Rambler motorhomes because an improperly secured wire harness may cause a fire.
Product
FLEETWOOD — FLEETWOOD, HOLIDAY RAMBLER DISCOVERY, NAVIGATOR, ENDEAVOR, DISCOVERY LXE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0526-2020·2019-12-04
Zimmer Biomet Recalls Custom Medical Devices Due to Cleaning Issues
Zimmer Biomet is recalling various custom medical devices because elevated levels of bacterial endotoxin and residual debris remain on the products due to a cleaning issue.
Product
Various Custom Products, Item Nos. CP102940 CP102941 CP102942 CP102943 CP102944 CP102945 CP102946 CP102947 CP102948 CP112662 CP112663 CP112664 CP112674 CP112675 CP113771 CP113777 CP113778 CP113782 CP113783 CP114083 CP114090 CP114112 CP114118 CP114148…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0584-2020·2019-12-04
GN Hearing Recalls In-the-Ear Hearing Aids Due to Software Bug
GN Hearing is recalling 285 in-the-ear hearing aids because a software bug in a repair tool altered sound amplification specifications, potentially increasing gain.
Product
In-the-Ear hearing aids, Model Numbers: T9ITC-DW-LP, FT6ITC-D-MP, FT6ITE-D-MP, FT8CIC-MP, FT8ITC-W-HP, FT8ITC-W-LP, FT8ITC-W-MP, FT8ITE-DW-HP, FT8MIH-W-HP, FT8MIH-W-MP, LT5CIC-MP, LT5CIC-UP, LT5IIC-LP, LT5ITC-DW-MP, LT5ITC-DW-UP, LT5ITE-DW-HP, LT5ITE-DW-MP, LT5ITE-DW-UP…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0520-2020·2019-12-04
Zimmer Biomet Recalls Shoulder Baseplates Due to Cleaning Issues
Zimmer Biomet is recalling COMP RVRS Shoulder Baseplates because elevated levels of bacterial endotoxin and residual debris remain on the devices due to a cleaning issue.
Product
COMP RVRS Shoulder Baseplates, including Custom Products, Item numbers 115331S 115331 115330S 115330 110040610 110040620 010000589 CP561861 PM0001456 PM551047 PM551063 PM555137 PM555160 PM555209 PM555322 PM555406 PM555415 UDI…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0533-2020·2019-12-04
Zimmer Biomet Recalls Custom Shoulder Implants Due to Cleaning Issues
Zimmer Biomet is recalling specific custom shoulder replacement implants because elevated levels of bacterial endotoxin and residual debris remain on the devices due to a cleaning issue.
Product
BIOMOD PORCOAT HA GLENTRAY; Custom Shoulder Products Item Nos. PM0000097 PM555140 PM555147 PM555319 PM555418 113867 113865 113863 Product Usage: Total Shoulder Replacement
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0528-2020·2019-12-04
Zimmer Biomet Recalls HA Pins and Hoffman/Colles Pins Due to Cleaning Issues
Zimmer Biomet is recalling HA Pins and Hoffman/Colles Pins because elevated bacterial endotoxin and residual debris remain on the devices due to a cleaning issue.
Product
HA Pins (DFS HA Cort Screw), Hoffman/Colles Pins (Colles CSER Sterile w/ Pin Kit) Item Nos: HAA60-09030 HAA60-09040 HAA60-10030 HAA60-10040 HAA60-11030 HAA60-11040 HAA60-11050 HAA60-12040 HAA60-12060 HAA60-13030 HAA60-13040 HAA60-13050 HAA60-13060 HAA60-13070…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0523-2020·2019-12-04
Zimmer Biomet Recalls Hip Systems Due to Cleaning Issues
Zimmer Biomet is recalling various hip arthroplasty systems because elevated levels of bacterial endotoxin and residual debris remain on the devices due to a cleaning issue.
Product
Various Hip systems, Item Nos. 104207 104212 104215 11-162809 11-162810 11-162811 11-162812 11-162813 21-103202 21-103203 21-103204 21-103205 21-103206 21-103207 21-103208 21-103209 21-103210 21-103211 21-103212 21-103215 21-104109 21-104110 21-104111…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0522-2020·2019-12-04
Zimmer Biomet Recalls Hennessy Left Constrained Glenoid Shoulder Implants
Zimmer Biomet is recalling Hennessy Left Constrained Glenoid Humeral Shoulder Implants due to elevated bacterial endotoxin and residual debris caused by a cleaning issue.
Product
HENNESSY LEFT CONST GLENOID HA, Item No. PM555360 UDI (01)00880304819597(17)260425(10)664030 Product Usage: Constrained Shoulder.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0531-2020·2019-12-04
Zimmer Biomet Recalls Guide Wires Due to Bacterial Endotoxin and Debris
Zimmer Biomet is recalling 2.0mm Ball Nose Guide Wires because elevated levels of bacterial endotoxin and residual debris remain on the devices due to a cleaning issue.
Product
2.0MM BALL NOSE GUIDE WIRE, Item Nos. 281017006 - Product Usage: These instruments and delivery systems are used to facilitate implantation of orthopedic medical devices.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0530-2020·2019-12-04
Zimmer Biomet Recalls Ball Nose Guide Wires Due to Cleaning Issues
Zimmer Biomet is recalling Ball Nose Guide Wires because elevated levels of bacterial endotoxin and residual debris remain on the devices due to a cleaning issue.
Product
BALL NOSE GUIDE WIRE 80CM, 100CM. Item Nos. 281001080 281001100 Product Usage: These instruments and delivery systems are used to facilitate implantation of orthopedic medical devices.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0580-2020·2019-12-04
Boston Scientific Recalls Rebel Monorail Coronary Stent Systems
Boston Scientific is recalling 14,145 Rebel Monorail PtCr Coronary Stent Systems because they may be missing a hydrophilic coating step.
Product
Rebel Monorail PtCr Coronary Stent System, REF / Catalog No. H7493927324300, Rebel MR OUS 3.0mm x 24mm. The Rebel Monorail (MR) Stent System is a balloon expandable Platinum Chromium (PtCr) Alloy stent pre-mounted on a Monorail Catheter.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0583-2020·2019-12-04
GN Hearing Recalls Behind-the-Ear Hearing Aids Due to Software Bug
GN Hearing is recalling 590 behind-the-Ear hearing aids because a software bug in a repair tool altered sound amplification specifications, potentially increasing gain.
Product
Behind-the-Ear hearing aids, Model Numbers: Q962-DRW, T561-DRW, T562-DRW, T762-DRW, T777-DW, AMZ964-DRW, ET588-DWH, ET598-DW, ET788-DWH, ET798-DW, ET988-DWH, ET998-DW, FT861-DRW, FT862-DRW, RE561-DRWC, RE762-DRW, RE961-DRWC, RE962-DRW, PZ862-DRW, LT561-DRW, LT561-DRWZ…
Category
Medical Device
Distribution
Distributed nationwide