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.

42026–42050 of 80187

SevereFDA (Devices)·Z-1554-2018·2018-05-16
Vyaire Medical Recalls Pediatric AirLife Resuscitation Devices Due to Mask Sticking
Vyaire Medical is recalling 8,058 pediatric AirLife resuscitation devices because the mask may stick to the elbow, making it difficult or impossible to disconnect.
Product
AirLife Resuscitation, Pediatric, with mask, 40inch oxygen reservoir tubing, pressure-relief valve Product Usage: The AirLife Resuscitation devices are manual resuscitation devices that are used to provide positive pressure ventilation to patients who are not breathing or…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1714-2018·2018-05-16
Datascope recalls Better Bladder device due to seal separation risk
Datascope is recalling the Better Bladder device because seal separation may allow air to enter the housing, potentially collapsing the balloon and reducing ECMO blood flow.
Product
BEQ-TOP 22701, Catalog No. 701050790
Category
Medical Device
Distribution
13 states
SevereFDA (Devices)·Z-1556-2018·2018-05-16
Vyaire Medical Recalls AirLife Infant Resuscitation Devices Due to Mask Sticking
Vyaire Medical is recalling 180 AirLife Infant Resuscitation devices because the mask may stick to the elbow, making it difficult to disconnect.
Product
AirLife Resuscitation, Infant, with mask, 40inch oxygen reservoir tubing, pressure-relief valve, manometer Product Usage: The AirLife Resuscitation devices are manual resuscitation devices that are used to provide positive pressure ventilation to patients who are not…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1483-2018·2018-05-16
Draeger Fabius Tiro Anesthesia Machines Recalled for Ventilation Failure Risk
Draeger Medical is recalling 26 Fabius Tiro anesthesia machines because automatic ventilation may fail if motor position detection is disturbed.
Product
Fabius Tiro, anesthesia machine, catalog no. 8606000 Product Usage: The products are inhalation anesthesia machines for use in operating, induction and recovery rooms. They may be used with O2, N2O, and AIR supplied by a medical gas pipeline system or by externally mounted…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1716-2018·2018-05-16
Datascope Recalls Custom Tubing Packs Due to Potential Seal Separation
Datascope is recalling 22 units of BEQ-TOP 33700 ECC 3/8" PACK custom tubing kits because a seal defect may cause balloon collapse and reduced blood flow.
Product
BEQ-TOP 33700 ECC 3/8" PACK, Custom Tubing Pack with Bioline Coating, Catalog No. 701053845
Category
Medical Device
Distribution
13 states
SevereFDA (Food)·F-1391-2018·2018-05-16
Labrada Nutrition Recalls Lean Pro 8 Vanilla Protein Powder for Undeclared Egg
Labrada Nutrition is recalling specific lots of Lean Pro 8 Vanilla protein powder due to undeclared egg, a major food allergen.
Product
Lean Pro 8 Vanilla 2,268g (5lb) Tub
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1568-2018·2018-05-16
Vyaire Medical Recalls AirLife Resuscitation Devices Due to Mask Sticking
Vyaire Medical is recalling AirLife Resuscitation devices because the mask may stick to the elbow, making it difficult to disconnect.
Product
AirLife Resuscitation, Adult, with mask, oxygen reservoir bag, PEEP valve Product Usage: The AirLife Resuscitation devices are manual resuscitation devices that are used to provide positive pressure ventilation to patients who are not breathing or cannot adequately breathe…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1707-2018·2018-05-16
Datascope recalls Better Bladder device in custom tubing kits
Datascope is recalling the Better Bladder device in some custom tubing kits because seal separation may cause the balloon to collapse, potentially reducing blood flow in ECMO circuits.
Product
Small Patient ECC Pack BEQ-TOP 22301, Catalog No. 701049513
Category
Medical Device
Distribution
13 states
SevereFDA (Devices)·Z-1713-2018·2018-05-16
Datascope Recalls Better Bladder Device in Custom Tubing Kits
Datascope is recalling the Better Bladder device in custom tubing kits because seal separation may cause balloon collapse and reduced blood flow.
Product
BO-TOP 20705 SMALL PATIENT 1/4, Catalog No. 701053486
Category
Medical Device
Distribution
13 states
SevereFDA (Devices)·Z-1718-2018·2018-05-16
Datascope Recalls Custom Tubing Kits Due to Potential Balloon Collapse
Datascope is recalling 10 custom tubing kits because a seal defect may allow air to enter the housing, causing the balloon to collapse and reducing blood flow in ECMO circuits.
Product
BEQ-TOP 8504 1/4X1/4 PACK W/QP, Custom Tubing Kit, Catalog No. 701066949R02
Category
Medical Device
Distribution
13 states
SevereFDA (Devices)·Z-1566-2018·2018-05-16
Vyaire Medical Recalls AirLife Infant Resuscitators Due to Mask Sticking
Vyaire Medical is recalling 3,600 AirLife Infant Resuscitators because the mask may stick to the elbow, making it difficult to disconnect.
Product
AirLife Resuscitation, Infant, with mask, oxygen reservoir bag, pressure-relief valve Product Usage: The AirLife Resuscitation devices are manual resuscitation devices that are used to provide positive pressure ventilation to patients who are not breathing or cannot…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1484-2018·2018-05-16
Draeger Fabius Tiro M Anesthesia Machine Recalled for Ventilator Failure Risk
Draeger Medical is recalling one Fabius Tiro M anesthesia machine because automatic ventilation may fail if motor position detection is disturbed.
Product
Fabius Tiro M, anesthesia machine, catalog no. 8608400 Product Usage: The products are inhalation anesthesia machines for use in operating, induction and recovery rooms. They may be used with O2, N2O, and AIR supplied by a medical gas pipeline system or by externally mounted…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1401-2018·2018-05-16
FDA Recalls Energique Herbal Supplements for Unapproved Drug Claims
Grato Holdings is recalling Energique herbal supplements because they are marketed as unapproved new drugs based on disease claims.
Product
Energique, Herbal Supplement, Octocom,; Dist. by Energique, Inc. Woodbine, IA 51579
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1730-2018·2018-05-16
Datascope Recalls Custom Tubing Kits Due to Potential Balloon Collapse
Datascope is recalling 18 custom tubing kits because a seal defect may cause the Better Bladder balloon to collapse, potentially reducing blood flow in ECMO circuits.
Product
BEQ-TOP 41201 ECC 3/8 PUMP PAC, Custom Tubing Kit, Catalog No. 701064867
Category
Medical Device
Distribution
13 states
SevereFDA (Devices)·Z-1559-2018·2018-05-16
Vyaire Medical Recalls AirLife Infant Resuscitation Devices Due to Mask Sticking
Vyaire Medical is recalling 8,124 AirLife Infant Resuscitation devices because the mask may stick to the elbow, making it difficult or impossible to disconnect.
Product
AirLife Resuscitation, Infant, with mask, 40inch oxygen reservoir tubing, pressure-relief valve, CO2 monitor, monometer Product Usage: The AirLife Resuscitation devices are manual resuscitation devices that are used to provide positive pressure ventilation to patients who…
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·18T006000·2018-05-16
Continental Recalls Specific Tires Due to Visible Cords and Crash Risk
Continental Tire is recalling specific Conti Hybrid HS3 tires because visible cords may cause sudden air loss, increasing the risk of a crash.
Product
TIRES recall
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1572-2018·2018-05-16
Vyaire Medical Recalls Pediatric AirLife Resuscitation Devices Due to Mask Sticking
Vyaire Medical is recalling 720 pediatric AirLife resuscitation devices because the mask may stick to the elbow, making it difficult to disconnect.
Product
AirLife Resuscitation, Pediatric, with mask, 40inch oxygen reservoir tubing, pressure-relief valve, PEEP valve Product Usage: The AirLife Resuscitation devices are manual resuscitation devices that are used to provide positive pressure ventilation to patients who are not…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1733-2018·2018-05-16
Datascope recalls custom pediatric ECMO tubing kits due to seal defect
Datascope is recalling two custom pediatric ECMO tubing kits because a seal defect may allow air to enter the device, potentially reducing blood flow.
Product
BEQ-TOP 50903 Custom ECC Pack-Pedriatric , Custom Tubing Kit, Catalog No. 709000078
Category
Medical Device
Distribution
13 states
SevereFDA (Devices)·Z-1711-2018·2018-05-16
Datascope Better Bladder Device Recalled Due to Seal Separation Risk
Datascope is recalling Better Bladder devices in custom tubing kits because seal separation may cause balloon collapse and reduced ECMO blood flow.
Product
BEQ-TOP 40700 HUNTINGTON, Catalog No. 701062899
Category
Medical Device
Distribution
13 states
SevereFDA (Devices)·Z-1723-2018·2018-05-16
Datascope Recalls Better Bladder Custom Tubing Kits Due to Seal Separation
Datascope Corporation is recalling 10 units of the BEQ-T 25501 Better Bladder Pack, Custom Tubing Kit. A seal defect may allow air entry, causing balloon collapse and reduced blood flow in ECMO circuits.
Product
BEQ-T 25501 3/8" Better Bladder Pack, Custom Tubing Kit, Catalog No. 709000370
Category
Medical Device
Distribution
13 states
SevereFDA (Drugs)·D-0801-2018·2018-05-16
Coast Quality Pharmacy Recalls MAA Kits Due to Sterility Concerns
Coast Quality Pharmacy LLC is recalling 52 vials of Macroaggregated albumin (MAA) kits due to a lack of assurance of sterility. The affected products were distributed to six states.
Product
Macroaggregated albumin (MAA) kit (for the preparation of Tc99m MAA), Aggregated and non-Aggregated Human Serum Albumin 2.5-5 mg Sodium Acetate Sol 200 mL/0.125 mL lyophilized powder in 10 mL glass vial, Rx only, AnazaoHealth, Tampa, FL
Category
Medical Device
Distribution
6 states
SevereFDA (Devices)·Z-1575-2018·2018-05-16
Vyaire Medical Recalls Pediatric AirLife Resuscitation Devices Due to Mask Sticking
Vyaire Medical is recalling 270 pediatric AirLife resuscitation devices because the mask may stick to the elbow, making it difficult or impossible to disconnect.
Product
AirLife Resuscitation, Pediatric, with mask, oxygen reservoir bag, manometer, pressure-relief valve, PEEP valve Product Usage: The AirLife Resuscitation devices are manual resuscitation devices that are used to provide positive pressure ventilation to patients who are not…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1558-2018·2018-05-16
Vyaire Medical Recalls AirLife Pediatric Resuscitation Devices Due to Mask Sticking
Vyaire Medical is recalling 42 AirLife Pediatric Resuscitation devices because the mask may stick to the elbow, making it difficult or impossible to disconnect.
Product
AirLife Resuscitation, Pediatric, with mask, 40inch oxygen reservoir tubing, pressure-relief valve, CO2 monitor, monometer Product Usage: The AirLife Resuscitation devices are manual resuscitation devices that are used to provide positive pressure ventilation to patients who…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1699-2018·2018-05-16
Siemens Recalls Syngo.plaza Software to Prevent Patient Misdiagnosis
Siemens Medical Solutions is recalling Syngo.plaza software due to format errors in study dates and issues with legacy presentation states that could lead to patient misdiagnosis.
Product
Syngo.plaza software VB10A model numbers: 10863171, 10863172, 10863173 Syngo.Plaza is a Picture Archiving and Communication System (PACS) intended to display, process, read, report, communicate, distribute, store and archive digital medical images. It supports the physician…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1728-2018·2018-05-16
Datascope Recalls Custom Tubing Kits Due to Potential Balloon Collapse
Datascope Corporation is recalling BEQ-TOP 22301 Custom Tubing Kits because seal separation may allow air to enter the housing, causing the balloon to collapse and reducing blood flow.
Product
BEQ-TOP 22301, Custom Tubing Kit, Catalog No. 701049513
Category
Medical Device
Distribution
13 states