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.

43026–43050 of 80187

SevereFDA (Devices)·Z-1171-2018·2018-03-07
Circulatory Technology Recalls Cardiopulmonary Bypass Blood Reservoirs
Circulatory Technology Inc is recalling specific models of cardiopulmonary bypass blood reservoirs because they may collapse during use, potentially causing a drop in circuit blood flow.
Product
**Recall Expanded to add these models: Bigger Better-Bladder cardiopulmonary bypass blood reservoir; Models: BBB38 (individual, sterile, pouched) and BBB38NS (sold bulk to kit manufacturers)
Category
Medical Device
Distribution
20 states
SevereNHTSA·18V155000·2018-03-07
New Flyer Recalls Transit Buses Due to Drive Shaft End-Cap Failure Risk
New Flyer is recalling 2016-2018 XDE40, XDE60, and 2017 XDE35 buses because plastic drive shaft end-caps may crack, causing loss of drive power and increasing crash risk.
Product
NEW FLYER — NEW FLYER XDE40, XDE60, XDE35
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18E012000·2018-03-07
S&B Filters Recalls Cold Air Intake Kits for Ford Trucks
S&B Filters is recalling specific Cold Air Intake Kits for Ford Super Duty trucks because a missing hole in the battery tray may prevent proper grounding, increasing fire risk.
Product
EQUIPMENT recall
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0547-2018·2018-03-07
Fagron Recalls SyrSpend SF Suspending Base Due to Microbial Contamination
Fagron, Inc. is recalling SyrSpend SF Suspending Base because the product was found to be contaminated with yeast and mold.
Product
SyrSpend SF Suspending Base, a) 500 mL (NDC 51552-1079-5) and b) 4 L (NDC 51552-1079-9), Rx Only, Manufactured by Fagron Inc. St. Paul, MN 55120
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0732-2018·2018-03-07
Ventana ultraView SISH Detection Kit Recalled for Leaking Reagent Dispensers
Ventana Medical Systems is recalling 6 units of the ultraView SISH Detection Kit due to increased reports of leaking and sticking reagent dispensers.
Product
ultraView SISH Detection Kit, Ventana Part Number 780-001, Roche GMMI 05271967001 in vitro diagnostic
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0774-2018·2018-03-07
Zimmer Biomet Recalls Antegrade Femoral Nail Instrument Kits
Zimmer Biomet is recalling 337 Antegrade Femoral Nail Instrument Kits because a bolt may fracture during use, potentially affecting patients undergoing orthopedic surgery.
Product
14-442000S Antegrade Femoral Nail Instrument Kit, orthopedic instrument
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0740-2018·2018-03-07
Ventana Medical Systems Recalls NEXES VEN IVIEW DAB DET KT JPN-US EXPORT
Ventana Medical Systems is recalling NEXES VEN IVIEW DAB DET KT JPN-US EXPORT in vitro diagnostic kits due to increased reports of leaking and sticking reagent dispensers.
Product
NEXES VEN IVIEW DAB DET KT JPN-US EXPORT, Ventana Part Number 760-041, Roche GMMI 05266084001 in vitro diagnostic
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·18E013000·2018-03-07
Norcold Recalls RV Refrigerators Due to Propane Leak Risk
Norcold is recalling specific RV refrigerators because loose gas valve screws may allow propane to leak into the passenger compartment, creating a fire risk.
Product
EQUIPMENT:RECREATIONAL VEHICLE/TRAILER recall
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0739-2018·2018-03-07
Ventana ultraView SISH DNP Detection Kit Recalled for Leaking Reagent Dispensers
Ventana Medical Systems Inc is recalling 358 units of the ultraView SISH DNP Detection Kit due to increased reports of leaking and sticking reagent dispensers.
Product
ultraView SISH DNP Detection Kit, Ventana Part Number 800-098, Roche GMMI 05907136001 in vitro diagnostic
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0817-2018·2018-03-07
Circulatory Technology Recalls Better-Bladder ECMO Blood Reservoirs
Circulatory Technology Inc is recalling Better-Bladder cardiopulmonary bypass blood reservoirs because they may collapse during use, potentially causing a drop in circuit blood flow.
Product
Better-Bladder cardiopulmonary bypass blood reservoir; Models: BB14 (individual, sterile, pouched) and BB14NS (sold bulk to kit manufacturers)
Category
Medical Device
Distribution
20 states
SevereNHTSA·18V156000·2018-03-07
Nissan Recalls 2011-2012 Juke Vehicles for Fuel Leak Risk
Nissan is recalling 2011-2012 Juke vehicles because a previous repair may have left the fuel pressure sensor loose, creating a potential fire hazard.
Product
NISSAN — NISSAN JUKE
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0544-2018·2018-03-07
Acyclovir Tablets Recalled Due to Presence of Torsemide Tablets
Apace KY LLC is recalling 630 cartons of Acyclovir 400 mg tablets because some blister cavities may contain Torsemide tablets instead.
Product
ACYCLOVIR — ACYCLOVIR (ACYCLOVIR)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0549-2018·2018-03-07
B. Braun Recalls Sodium Chloride Irrigation Due to Particulate Matter
B. Braun Medical Inc. is recalling 17,360 units of 0.9% Sodium Chloride Irrigation USP due to the presence of polyethylene particulate matter.
Product
SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0734-2018·2018-03-07
Ventana Recalls CINtec PLUS Cytology Kit Due to Leaking Reagent Dispensers
Ventana Medical Systems is recalling 748 units of the CINtec PLUS Cytology Kit due to increased reports of leaking and sticking reagent dispensers.
Product
CINtec PLUS Cytology Kit (CE-IVD), Ventana Part Number 605-100, Roche GMMI 06889565001 in vitro diagnostic
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0713-2018·2018-03-07
Siemens SOMATOM Go.Up CT Table Recall for Potential Instability
Siemens Medical Solutions is recalling six SOMATOM Go.Up CT system tables because improperly tightened bolts may loosen, causing the table to become unstable.
Product
SOMATOM Go.Up computed tomography (CT) x-ray system table, Model Number: 11061628 Product Usage: Intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data. The images delivered by these systems can be used by a…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0715-2018·2018-03-07
Mobius AIRO Mobile CT System Recalled for Unintended Motion Risk
Mobius Imaging is recalling 105 AIRO Mobile CT Systems due to a risk of unintended device motion during startup or scan preparation.
Product
AIRO Mobile CT System, Model Number: MobiCT-32 Product Usage: The AIRO¿ is intended to be used for X-ray computed tomography applications for anatomy that can be imaged in the 107cm aperture excluding pediatric patients and patients weighing over 400 lbs. (182 kg).
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0736-2018·2018-03-07
Ventana OptiView Amplification Kit Recalled for Leaking and Sticking Reagent Dispensers
Ventana Medical Systems is recalling OptiView Amplification Kits due to increased reports of leaking and sticking reagent dispensers.
Product
OptiView Amplification Kit, Ventana Part Number 760-099, Roche GMMI 06396518001 in vitro diagnostic
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0731-2018·2018-03-07
Ventana iView DAB IHC Detection Kit Recalled for Leaking and Sticking
Ventana Medical Systems is recalling iView DAB IHC Detection Kits due to increased reports of leaking and sticking reagent dispensers.
Product
iView DAB IHC Detection Kit, Ventana part Number 760-091, Roche GMMI 05266157001 in vitro diagnostic
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0729-2018·2018-03-07
Ventana OptiView DAB IHC Detection Kit Recalled for Leaking and Sticking
Ventana Medical Systems is recalling OptiView DAB IHC Detection Kits due to increased reports of leaking and sticking reagent dispensers.
Product
OptiView DAB IHC Detection Kit, Ventana Part Number 760-700, Roche GMMI 06396500001 in vitro diagnostic
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0737-2018·2018-03-07
Ventana OptiView Amplification Kit Recalled for Leaking and Sticking Reagent Dispensers
Ventana Medical Systems is recalling OptiView Amplification Kits due to increased reports of leaking and sticking reagent dispensers.
Product
OptiView Amplification Kit (250 Test), Ventana Part Number 860-099, Roche GMMI 06718663001 in vitro diagnostic
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0733-2018·2018-03-07
Ventana ultraView SISH DNP Detection Kit Recalled for Leaking Reagent Dispensers
Ventana Medical Systems is recalling 20 units of the ultraView SISH DNP Detection Kit due to increased reports of leaking and sticking reagent dispensers.
Product
ultraView SISH DNP Detection Kit US, Ventana Part Number 760-098, Roche GMMI 05572037001 in vitro diagnostic
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0730-2018·2018-03-07
Ventana ultraView Universal DAB Detection Kit Recalled for Leaking Reagent Dispensers
Ventana Medical Systems is recalling ultraView Universal DAB Detection Kits due to increased reports of leaking and sticking reagent dispensers.
Product
ultraView Universal DAB Detection Kit, Ventana part Number 760-500, Roche GMMI 05269806001 in vitro diagnostic
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0735-2018·2018-03-07
Ventana Recalls CINtec PLUS Cytology Kits Due to Leaking Reagent Dispensers
Ventana Medical Systems is recalling 18 units of the CINtec PLUS Cytology Kit due to increased reports of leaking and sticking reagent dispensers.
Product
CINtec PLUS Cytology Kit (Canada/Japan), Ventana Part Number 805-100, Roche GMMI 06889549001 in vitro diagnostic
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0714-2018·2018-03-07
Siemens CT Table Recalled Due to Potential Bolt Loosening and Instability
Siemens Medical Solutions is recalling SOMATOM Go.Now CT system tables because bolts may loosen, causing the table to become unstable.
Product
SOMATOM Go.Now computed tomography (CT) x-ray system table, Model Number: 11061618 Product Usage: Intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data. The images delivered by these systems can be used by a…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0710-2018·2018-03-07
Siemens Medical Solutions Recalls Artis zee and Artis zeego Foot Switches
Siemens Medical Solutions is recalling 510 foot switch accessories for Artis zee and Artis zeego x-ray systems because they may fail to release radiation.
Product
Artis zee and Artis zeego model Interventional fluoroscopic x-ray foot switch accessory; Model Numbers: 4787797, 4787805, and 4787813.
Category
Medical Device
Distribution
52 states