State

Alabama product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

42876–42900 of 80187

ModerateFDA (Devices)·Z-1042-2018·2018-03-21
Zimmer Biomet Recalls Hip and Knee Implants Due to Packaging Residue
Zimmer Biomet is recalling 13,227 hip and knee implants because LDPE packaging may leave residue on the polished surfaces.
Product
CR OPTION FEM COMP SIZE C/L CR OPTION FEM COMP SIZE C/R CR OPTION FEM COMP SIZE D/L CR OPTION FEM COMP SIZE D/R CR OPTION FEM COMP SIZE E/L CR OPTION FEM COMP SIZE E/R CR OPTION FEM COMP SIZE F/L CR OPTION FEM COMP SIZE F/R CR OPTION FEM COMP SIZE G/L CR OPTION FEM COMP…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1044-2018·2018-03-21
Zimmer Biomet Recalls LPS-FLEX Knee Implants Due to Packaging Residue
Zimmer Biomet is recalling 13,227 LPS-FLEX knee implants because LDPE packaging may leave residue on the polished surface.
Product
LPS-FLEX PRECOAT FEMORAL B-R LPS-FLEX PRECOAT FEMORAL C-L LPS-FLEX PRECOAT FEMORAL C-R LPS-FLEX PRECOAT FEMORAL D-L LPS-FLEX PRECOAT FEMORAL D-R LPS-FLEX PRECOAT FEMORAL E-L LPS-FLEX PRECOAT FEMORAL E-R LPS-FLEX PRECOAT FEMORAL F-L LPS-FLEX PRECOAT FEMORAL F-R LPS-FLEX…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1039-2018·2018-03-21
Zimmer Biomet Recalls Hip and Knee Implants Due to Packaging Residue
Zimmer Biomet is recalling specific hip and knee implants because LDPE packaging may leave residue on the polished surfaces.
Product
LPS PRECOAT SRF HDN FEM SZ D-L LPS PRECOAT SRF HDN FEM SZ D-R LPS PRECOAT SRF HDN FEM SZ E-L LPS POROUS SRF HDN FEM SZ D-LT LPS POROUS SRF HDN FEM SZ E-LT This device is indicated for patients with severe knee pain and disability
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1032-2018·2018-03-21
Zimmer Biomet Recalls Hip and Knee Implants Due to Packaging Residue
Zimmer Biomet is recalling 13,227 hip and knee implants because LDPE packaging may leave residue on the polished surfaces.
Product
CR-FLEX POR HATCP FEM C-L CR-FLEX POR HATCP FEM C-R CR-FLEX POR HATCP FEM D-L CR-FLEX POR HATCP FEM D-R CR-FLEX POR HATCP FEM E-L CR-FLEX POR HATCP FEM E-R CR-FLEX POR HATCP FEM F-L CR-FLEX POR HATCP FEM F-R CR-FLEX POR HATCP FEM G-L CR-FLEX POR HATCP FEM G-R This…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1058-2018·2018-03-21
Zimmer Biomet Recalls Knee Implants Due to Packaging Residue
Zimmer Biomet is recalling 13,227 CR-FLEX knee implants because LDPE packaging may leave residue on the polished surface.
Product
CR-FLEX GSF PCT SZ C-R MINUS¿ CR-FLEX GSF PCT SZ D-L MINUS¿ CR-FLEX GSF PCT SZ D-R MINUS¿ CR-FLEX GSF PCT SZ E-L MINUS¿ CR-FLEX GSF PCT SZ E-R MINUS¿¿ CR-FLEX GSF PCT SZ F-L MINUS¿ CR-FLEX GSF PCT SZ F-R MINUS¿ CR-FLEX GSF PCT SZ G-L MINUS¿ CR-FLEX GSF PCT SZ G-R MINUS¿…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0599-2018·2018-03-21
Novel Laboratories Recalls Hydrocodone Bitartrate and Homatropine Methylbromide Tablets
Novel Laboratories is recalling specific lots of Hydrocodone Bitartrate and Homatropine Methylbromide tablets due to failed impurities and degradation specifications.
Product
HYDROCODONE BITARTRATE AND HOMATROPINE METHYLBROMIDE — HYDROCODONE BITARTRATE AND HOMATROPINE METHYLBROMIDE (HYDROCODONE BITARTRATE AND HOMATROPINE METHYLBROMIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1057-2018·2018-03-21
Zimmer Biomet Recalls NEXGEN GSF Porous Femoral LPS Flex Implants
Zimmer Biomet is recalling NEXGEN GSF Porous Femoral LPS Flex implants because LDPE packaging may leave residue on the polished surface.
Product
NEXGEN GSF POROUS FEMORAL LPS FLEX SIZE F, RIGHT¿ " These devices are indicated for patients with: - Painful and/or disabling knee joints due to osteoarthritis or traumatic arthritis. - Previous tibial condyle or plateau fractures with loss of anatomy or function. - Varus or…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0969-2018·2018-03-21
Randox Recalls Immunoassay Premium Controls Due to Stability Claim Failure
Randox Laboratories is recalling 117 kits of Immunoassay Premium Controls because the ACTH component does not meet the stated reconstituted stability claim in the product instructions for use.
Product
Immunoassay Premium Controls (3x4x5mL and 12x5mL packages)
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0936-2018·2018-03-21
Medtronic Recalls Argyle Suction Tubing Due to Incorrect Packaging Labeling
Medtronic is recalling 58,954 units of Argyle Suction Tubing because some pouches may be incorrectly labeled as Salem Sump Dual Lumen Stomach Tubes.
Product
Argyle Suction Tubing (Product # 8888301515) Argyle Suction Tubing is an extruded tube used as an extension for different types of devices in an operating room, bonded with 2 female sure grip connectors at each end of the tube to facilitate the plug/ insertion of the device…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0598-2018·2018-03-21
Dr. Reddy's Recalls Clocortolone Pivalate Cream Due to Stability Issues
Dr. Reddy's Laboratories is recalling Clocortolone Pivalate Cream, 0.1%, 90-gram tubes because viscosity failed stability specifications.
Product
Clocortolone Pivalate Cream, 0.1%, 90-gram tube, Rx only, Distributed by: Dr. Reddy's Laboratories, Inc. Princeton, NJ 08540, Manufactured by: DPT, Laboratories Ltd. San Antonio, TX 78215, NDC 43598-341-90
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0589-2018·2018-03-21
Psoriasin Daytime Relief Cream Recalled for Subpotent Coal Tar Content
Alva-Amco Pharmacal Companies is recalling Psoriasin Daytime Relief Cream because it failed to maintain its label claim of coal tar throughout its expiry period.
Product
Psoriasin Daytime Relief Cream with Vitamin D & Oatmeal, (Coal Tar 1.25%), packagedin 57 g plastic tubes, Distributed by: ALVA-AMCO Pharmacal Cos., Inc., Niles, IL 60714, USA. NDC 52389-745-56, UPC 0 72959 01045 4.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0970-2018·2018-03-21
Randox Immunoassay Premium Plus Controls Recalled for Stability Issues
Randox Laboratories is recalling Immunoassay Premium Plus Controls because the ACTH component does not meet the stability claims in the product instructions.
Product
Immunoassay Premium Plus Controls (3x4x5mL and 12x5mL packages)
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·18127·2018-03-20
Briggs & Stratton Recalls Riding Mowers Due to Reverse Mow Malfunction
Briggs & Stratton is recalling Snapper, Simplicity, and Massey Ferguson riding mowers because a malfunctioning switch may allow the mower to mow while reversing, posing a risk of injury.
Product
Snapper, Simplicity, and Massey Ferguson riding mowers
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·18V179000·2018-03-19
Forest River Recalls Motorhomes Due to Power Steering Hose Fire Risk
Forest River is recalling specific 2012-2017 motorhomes because an incorrectly routed power steering hose may rub against the starter motor, causing electrical arcing and a fire risk.
Product
FOREST RIVER — FOREST RIVER, COACHMEN, GLAVAL BUS CHARLESTON, BERKSHIRE, PATHFINDER, CROSS COUNTRY
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V182000·2018-03-19
McElrath Trailers Recalling 2013-2018 Models Due to Weld Failure Risk
McElrath Trailers is recalling specific 2013-2018 models because a weld on the trailer neck may fail, potentially causing loss of control and a crash.
Product
MCELRATH TRAILERS — MCELRATH TRAILERS VX50-800, 818I, VX30-800
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V181000·2018-03-19
Entegra Aspire Recalled for Power Steering Hose Fire Risk
Entegra Coach is recalling 2011-2012 and 2015-2016 Aspire motorhomes because an incorrectly routed power steering hose may cause electrical arcing and a fire.
Product
ENTEGRA — ENTEGRA ASPIRE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V183000·2018-03-19
REV Recalls 2018 Motorhomes Due to HVAC Fire Risk
REV Recreation Group is recalling 600 2018 motorhomes because HVAC wires may disconnect, creating a fire risk if reconnected incorrectly.
Product
MONACO — MONACO, AMERICAN COACH, FLEETWOOD SIGNATURE, MARQUIS, AMERICAN REVOLUTION, AMERICAN DREAM
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·18V180000·2018-03-19
Forest River Recalls 2018 No Boundaries Trailers Due to Spare Tire Mount Defect
Forest River is recalling 2018 No Boundaries recreational trailers because the spare tire mount may be too weak, risking tire detachment and road hazards.
Product
FOREST RIVER — FOREST RIVER NO BOUNDARIES
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·18731·2018-03-19
Carrier Recalls Commercial Rooftop HVAC Units Due to Fire Hazard
Carrier is recalling about 530 commercial rooftop HVAC units because a humidifier fan may fail to shut off, posing a fire hazard. No injuries have been reported.
Product
Carrier WeatherExpert commercial packaged rooftop HVAC units with humidimizer option
Category
Consumer Product
Distribution
Distributed nationwide
CriticalUSDA FSIS·023-2018·2018-03-16
Stampede Meat Recalls Beef Steaks Due to Salmonella Risk
Stampede Meat is recalling approximately 484,800 pounds of frozen raw beef top sirloin steaks because a seasoning ingredient tested positive for Salmonella.
Product
Stampede Culinary Partners, Inc. — SMI Holdings, Inc Recalls Beef Products Due to Possible Salmonella Contamination
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·18T002000·2018-03-16
Les Schwab Recalls Retreaded Truck Tires Due to Adhesion Defect
Les Schwab is recalling specific retreaded steel-belted radial truck tires because the vulcanizing compound may not have fully cured, increasing the risk of tread separation and crashes.
Product
TIRES recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V178000·2018-03-15
Hino Recalls 2018-2019 Trucks Due to Engine Valve Train Defect
Hino is recalling 2018-2019 NE8J, NJ8J, and NV8J trucks because engine valve train lock nuts may be loose, potentially causing engine damage and shutdown.
Product
HINO — HINO NJ8J, NV8J, NE8J
Category
Vehicle
Distribution
Distributed nationwide
SevereUSDA FSIS·022-2018·2018-03-15
Standard Meat Company Recalls Raw Beef Steaks Due to Salmonella Risk
Standard Meat Company is recalling raw beef top sirloin steaks that may be contaminated with Salmonella. The products were shipped to restaurants nationwide.
Product
Standard Meat Company — Standard Meat Company Recalls Beef Products Due to Possible Salmonella Contamination
Category
Food
Distribution
Distributed nationwide
SevereUSDA FSIS·021-2018·2018-03-15
Johnsonville Recalls Smoked Pork Sausage Due to Possible Plastic Contamination
Johnsonville is recalling approximately 109,603 pounds of smoked pork sausage products that may contain hard, green plastic pieces.
Product
Johnsonville, LLC — Johnsonville, LLC Recalls Smoked Pork Sausage Products due to Possible Foreign Matter Contamination
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·18V171000·2018-03-15
E-One Recalls Typhoon, Cyclone II, and Quest II Vehicles for Spindle Defect
E-One is recalling 2008-2015 Typhoon, Cyclone II, and Quest II vehicles because front axle spindles may crack and fail, potentially causing a wheel to separate.
Product
E-ONE — E-ONE TYPHOON, CYCLONE II, QUEST II
Category
Vehicle
Distribution
Distributed nationwide