State

Alabama product recalls

73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

39076–39100 of 80118

HighFDA (Devices)·Z-0460-2019·2018-11-21
Virtual Imaging RadPRO Mobile X-Ray System Recalled for Mount Separation Risk
Virtual Imaging is recalling 253 RadPRO Mobile 40kW Digital X-Ray Systems because the tube head may separate and fall off the unit.
Product
RadPRO(R) Mobile 40kW Digital X-Ray System - Model: SM-40HF-B-D-C Product Usage: Instrument is used to take diagnostic radiographic exposures of the skull, spinal column, chest, abdomen, extremities, and other body parts on both adult and pediatric subjects. Applications…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0438-2019·2018-11-21
Stryker Spirit Plus Bed Recall for Potential Entrapment Risk
Stryker is recalling 20,030 Spirit Plus hospital beds with high rail siderails due to non-compliance with safety standards and a potential risk of patient entrapment.
Product
The Spirit Plus Bed, Model 5600 Spirit Plus /with high rail siderail option
Category
Medical Device
Distribution
50 states
HighFDA (Devices)·Z-0441-2019·2018-11-21
R82 A/S Recalls Heron Toilet and Bath Chairs Due to Aluminum Gas Spring
R82 A/S is recalling 687 Heron toilet and bath chairs because they contain aluminum gas spring heads. The recall is a replacement campaign for these specific units.
Product
Heron toilet and bath chair Model 880505-01 & 880505-11
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0425-2019·2018-11-21
AROA Biosurgery Recalls OviTex 1S Reinforced BioScaffold Mesh Devices
AROA Biosurgery is recalling OviTex 1S Reinforced BioScaffold 16x20cm devices because the PGA suture material degraded, causing them to fail burst specifications.
Product
OviTex 1S Reinforced BioScaffold 16x20cm, Part Number F10256-1620G
Category
Medical Device
Distribution
8 states
HighFDA (Drugs)·D-0258-2019·2018-11-21
Sandoz Recalls Isosorbide Dinitrate Tablets Due to Cross Contamination
Sandoz Inc. is recalling 18,832 bottles of Isosorbide Dinitrate 20 mg tablets due to cross-contamination with other products.
Product
ISOSORBIDE DINITRATE — ISOSORBIDE DINITRATE (ISOSORBIDE DINITRATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0429-2019·2018-11-21
Wornick Company Recalls Fire Roasted Onion and Pepper Blend
The Wornick Company is recalling Chef Sensations Fire Roasted diced onion/pepper blend due to potential Salmonella and Listeria contamination.
Product
Chef Sensations Fire Roasted 1/2" diced onion/pepper blend Net Wt 20 lbs
Category
Food
Distribution
40 states
HighFDA (Devices)·Z-0422-2019·2018-11-21
AROA Biosurgery Recalls OviTex 1S Reinforced BioScaffold Devices
AROA Biosurgery is recalling OviTex 1S Reinforced BioScaffold devices because the suture material degraded, causing them to fail burst specifications.
Product
OviTex 1S Reinforced BioScaffold 6x10cm, Part Number F10256-0610G
Category
Medical Device
Distribution
8 states
HighFDA (Devices)·Z-0442-2019·2018-11-21
Arthrex Recalls 3.2mm Proximal Reamer Due to Potential Breakage During Use
Arthrex, Inc. is recalling 832 units of the 3.2mm Proximal Reamer/Cannulated Drill because the instrument may break during use.
Product
3.2mm Proximal Reamer/Cannulated Drill provided as part of the Fibulock Fibular Nail System Pack. FibuLock Nail Procedure Pack: Contains instrumentation for the implantation of the FibuLock implant. Contents include: Actuation Driver, 6.2mm Reamer, 3.2mm Reamer, 2 mm Drill…
Category
Medical Device
Distribution
30 states
HighFDA (Devices)·Z-0451-2019·2018-11-21
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Set Screw Malfunction
Zimmer Biomet is recalling 2,163 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.
Product
Affixus Hip Fracture Nail 125 Deg 10x165mm, Item Number 816710165 The Affixus Hip Fracture Nail System, comprised of short and long nails, provides surgeons with an intramedullary hip screw to stabilize fractures of the proximal femur.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0445-2019·2018-11-21
Luminex Recalls Verigene Blood Culture Gram-Positive Nucleic Acid Kits
Luminex Corporation is recalling 12,700 trays of Verigene Blood Culture Gram-Positive Nucleic Acid Kits due to a potential for false negative results.
Product
VERIGENE Blood Culture Gram-Positive Nucleic Acid Kits (packaged as five-pack carriers) Product Usage: In vitro diagnostic test for the simultaneous detection and identification of potentially pathogenic gram-positive bacteria.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0435-2019·2018-11-21
AROA Biosurgery Recalls OviTex 2S Reinforced BioScaffold Mesh Devices
AROA Biosurgery is recalling OviTex 2S Reinforced BioScaffold devices because the suture material degraded, causing them to fail burst specifications after 18 months.
Product
OviTex 2S Reinforced BioScaffold 10x12cm, Part Number F10258-1012G
Category
Medical Device
Distribution
8 states
HighFDA (Devices)·Z-0432-2019·2018-11-21
AROA Biosurgery Recalls OviTex 2S Reinforced BioScaffold Mesh Devices
AROA Biosurgery is recalling OviTex 2S Reinforced BioScaffold mesh devices because the suture material degraded, causing them to fail burst specifications.
Product
OviTex 2S Reinforced BioScaffold 18x22cm, Part Number F10258-1822G
Category
Medical Device
Distribution
8 states
HighFDA (Devices)·Z-0469-2019·2018-11-21
Tosoh AIA-900 Analyzer Recalled Due to Pickup Arm Malfunction
Tosoh Bioscience is recalling 393 AIA-900 Analyzers because a pickup arm malfunction can stop the device from testing patient samples, causing delays in results.
Product
AIA-900 Analyzer, Product code 022930, 022930R
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0449-2019·2018-11-21
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Set Screw Defect
Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.
Product
Affixus Hip Fracture Nail Left 130 Deg 11x300mm, Item Number 814611300 The Affixus Hip Fracture Nail System, comprised of short and long nails, provides surgeons with an intramedullary hip screw to stabilize fractures of the proximal femur.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0430-2019·2018-11-21
AROA Biosurgery Recalls OviTex 2S Reinforced BioScaffold Mesh Devices
AROA Biosurgery is recalling OviTex 2S Reinforced BioScaffold devices because the suture material may degrade, causing them to fail burst specifications.
Product
OviTex 2S Reinforced BioScaffold 10x20cm, Part Number F10258-1020G
Category
Medical Device
Distribution
8 states
HighFDA (Devices)·Z-0424-2019·2018-11-21
AROA Biosurgery Recalls OviTex 1S Reinforced BioScaffold Mesh Devices
AROA Biosurgery is recalling OviTex 1S Reinforced BioScaffold mesh devices because the suture material degraded, causing some units to fail burst specifications.
Product
OviTex 1S Reinforced BioScaffold 10x20cm, Part Number F10256-1020G
Category
Medical Device
Distribution
8 states
HighFDA (Devices)·Z-0421-2019·2018-11-21
AROA Biosurgery Recalls OviTex 1S Reinforced BioScaffold Mesh Devices
AROA Biosurgery is recalling OviTex 1S Reinforced BioScaffold 4x8cm devices because the PGA suture material degraded, causing the devices to fail burst specifications.
Product
OviTex 1S Reinforced BioScaffold 4x8cm, Part Number F10256-0408G
Category
Medical Device
Distribution
8 states
HighFDA (Devices)·Z-0418-2019·2018-11-21
AROA Biosurgery Recalls OviTex Reinforced BioScaffold Mesh Devices
AROA Biosurgery is recalling OviTex Reinforced BioScaffold mesh devices because the suture material degraded, causing them to fail burst specifications.
Product
OviTex Reinforced BioScaffold 10x20cm, Part Number F10254-1020G
Category
Medical Device
Distribution
8 states
HighFDA (Devices)·Z-0427-2019·2018-11-21
AROA Biosurgery Recalls OviTex 1S Reinforced BioScaffold Mesh Devices
AROA Biosurgery is recalling OviTex 1S Reinforced BioScaffold devices because the suture material degraded, causing them to fail burst specifications.
Product
OviTex 1S Reinforced BioScaffold 20x20cm, Part Number F10256-2020G
Category
Medical Device
Distribution
8 states
HighFDA (Devices)·Z-0416-2019·2018-11-21
AROA Biosurgery Recalls OviTex Reinforced BioScaffold Mesh Devices
AROA Biosurgery is recalling OviTex Reinforced BioScaffold mesh devices because the suture material degraded, causing some units to fail burst specifications.
Product
OviTex Reinforced BioScaffold 6x10cm, Part Number F10254-0610G
Category
Medical Device
Distribution
8 states
HighFDA (Devices)·Z-0428-2019·2018-11-21
AROA Biosurgery Recalls OviTex 2S Reinforced BioScaffold Devices
AROA Biosurgery is recalling OviTex 2S Reinforced BioScaffold devices because the suture material degraded, causing them to fail burst specifications.
Product
OviTex 2S Reinforced BioScaffold 6x10cm, Part Number F10258-0610G
Category
Medical Device
Distribution
8 states
HighFDA (Devices)·Z-0419-2019·2018-11-21
AROA Biosurgery Recalls OviTex Reinforced BioScaffold Mesh Devices
AROA Biosurgery is recalling OviTex Reinforced BioScaffold 16x20cm devices because the suture material degraded, causing them to fail burst specifications after 18 months.
Product
OviTex Reinforced BioScaffold 16x20cm, Part Number F10254-1620G
Category
Medical Device
Distribution
8 states
HighFDA (Devices)·Z-0423-2019·2018-11-21
AROA Biosurgery Recalls OviTex 1S Reinforced BioScaffold Mesh Devices
AROA Biosurgery is recalling OviTex 1S Reinforced BioScaffold devices because the suture material degraded, causing them to fail burst specifications.
Product
OviTex 1S Reinforced BioScaffold 10x12cm, Part Number F10256-1012G
Category
Medical Device
Distribution
8 states
HighFDA (Devices)·Z-0431-2019·2018-11-21
AROA Biosurgery Recalls OviTex 2S Reinforced BioScaffold Mesh Devices
AROA Biosurgery is recalling OviTex 2S Reinforced BioScaffold devices because the suture material degraded, causing them to fail burst specifications after 18 months.
Product
OviTex 2S Reinforced BioScaffold 16x20cm, Part Number F10258-1620G
Category
Medical Device
Distribution
8 states
HighFDA (Devices)·Z-0452-2019·2018-11-21
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Set Screw Issue
Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.
Product
Affixus Hip Fracture Nail 125 Deg 12x165mm, Item Number 816712165 The Affixus Hip Fracture Nail System, comprised of short and long nails, provides surgeons with an intramedullary hip screw to stabilize fractures of the proximal femur.
Category
Medical Device
Distribution
Distributed nationwide