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.

39501–39525 of 80118

HighFDA (Devices)·Z-0276-2019·2018-10-31
Medtronic O-arm 1000 2nd Edition Imaging System Software Recall
Medtronic is recalling O-arm 1000 2nd Edition Imaging Systems due to software anomalies affecting startup, communication, and image acquisition.
Product
O-arm 1000 2nd Edition Imaging System, BASE BASE OARM Bl70000027120R SYSTEM 120V RWK, Model Number Bl70000027120R Product Usage: The O-arm Imaging System is a mobile x-ray system designed for 2D fluoroscopic and 3D imaging and is intended to be used where a physician…
Category
Medical Device
Distribution
45 states
HighFDA (Devices)·Z-0205-2019·2018-10-31
ESAOTE MyLab Gamma Ultrasound System Recalled for Probe Overheating Risk
ESAOTE S.P.A. is recalling 10 MyLab Gamma, Model 7410 ultrasound systems because probe power monitoring settings may cause the probe head to overheat during continuous operation.
Product
MyLab Gamma, Model 7410
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·18V767000·2018-10-31
Keystone Recalls 2019 Crossroads Cruiser Trailers Due to Gas Leak Risk
Keystone RV Company is recalling 2019 Crossroads Cruiser recreational trailers because the water heater exhaust may allow carbon monoxide or propane gas to enter the living quarters.
Product
CROSSROADS — CROSSROADS CRUISER
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0210-2019·2018-10-31
Siemens APTIO Rack Input Module Recall for Missing Pacemaker Warning
Siemens Healthcare Diagnostics is recalling 441 APTIO Rack Input Modules because they may have been shipped without a warning label regarding potential interference with pacemaker functionality.
Product
APTIO RACK INPUT MODULE
Category
Medical Device
Distribution
38 states
HighFDA (Devices)·Z-0272-2019·2018-10-31
Medtronic Recalls O-arm 1000 2nd Edition Imaging Systems Due to Software Anomalies
Medtronic is recalling 596 O-arm 1000 2nd Edition Imaging Systems worldwide due to reported software anomalies affecting startup, motion control, and image acquisition.
Product
O-arm 1000 2nd Edition Imaging System, OARM ASSY Bl70000027R SYS PRODUCT RWK, Model Number Bl70000027R Product Usage: The O-arm Imaging System is a mobile x-ray system designed for 2D fluoroscopic and 3D imaging and is intended to be used where a physician benefits from 2D…
Category
Medical Device
Distribution
45 states
HighFDA (Devices)·Z-0208-2019·2018-10-31
DePuy Mitek Screw and Washer Depth Gauge Recalled for Design Offset
DePuy Mitek is recalling 401 Mitek Screw and Washer Depth Gauges because a design offset causes readings to be approximately 3.2mm shorter than the actual bone hole length.
Product
Mitek Screw and Washer Depth Gauge, Product Code 219024
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·19711·2018-10-31
CFMOTO Recalls 2018 ZFORCE Recreational Off-Highway Vehicles Due to Crash Hazard
CFMOTO is recalling approximately 1,800 2018 ZFORCE recreational off-highway vehicles because the throttle pedal may fail to return to idle, posing a crash risk.
Product
Recreational off-highway vehicles (ROVs)
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0207-2019·2018-10-31
Howmedica Recalls Tritanium TL Steerable Inserter Due to Locking Mechanism Failure
Howmedica Osteonics Corp. is recalling 58 units of the Tritanium TL Steerable Inserter because the locking mechanism may fail to function as intended due to lack of lubrication.
Product
Tritanium TL Steerable Inserter, Cat. No. 48930000, UDI 07613327381900 Product Usage: The TL Steerable Inserter is a Class 1 instrument which is provided in a non-sterile condition. The inserter is designed to enter the disc space, with a fixed engagement between the…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0216-2019·2018-10-31
Siemens StreamLab Refrigerated Storage Module Recall for Missing Warning Label
Siemens Healthcare Diagnostics is recalling StreamLab Refrigerated Storage Module 9000 units because they may have been shipped without a warning label regarding potential interference with pacemaker functionality.
Product
STREAMLAB - REFRIGERATED STORAGE MODULE 9000
Category
Medical Device
Distribution
38 states
HighFDA (Devices)·Z-0212-2019·2018-10-31
Siemens APTIO 15000 Refrigerated Storage Module Recall for Missing Warning Label
Siemens Healthcare Diagnostics is recalling 441 APTIO 15000 Refrigerated Storage Modules because they may have been shipped without a warning label regarding potential interference with pacemaker functionality.
Product
APTIO 15000 REFRIGERATED STORAGE MODULE
Category
Medical Device
Distribution
38 states
HighFDA (Devices)·Z-0215-2019·2018-10-31
Siemens StreamLab Automation Modules Recalled for Missing Pacemaker Warning Label
Siemens Healthcare Diagnostics is recalling 186 StreamLab Automation Modules because they may have been shipped without a warning label regarding potential interference with pacemaker functionality.
Product
STREAMLAB CORE UNIT / LYNX WITH IOM
Category
Medical Device
Distribution
38 states
HighFDA (Devices)·Z-0278-2019·2018-10-31
Medtronic Recalls O-arm 1000 2nd Edition Imaging Systems Due to Software Anomalies
Medtronic is recalling 596 O-arm 1000 2nd Edition Imaging Systems worldwide due to software anomalies affecting startup, communication, and imaging functions.
Product
O-arm 1000 2nd Edition Imaging System, BASE OARM Bl70000027230R SYSTEM 230V RWK, Model Number Bl70000027230R Product Usage: The O-arm Imaging System is a mobile x-ray system designed for 2D fluoroscopic and 3D imaging and is intended to be used where a physician benefits…
Category
Medical Device
Distribution
45 states
HighFDA (Devices)·Z-0204-2019·2018-10-31
ESAOTE MyLab Alpha Ultrasound System Recalled for Probe Overheating Risk
ESAOTE S.P.A. is recalling 10 MyLab Alpha Model 7400 ultrasound systems because probe power monitoring settings may cause the probe head to overheat during continuous operation.
Product
MyLab Alpha, Model 7400
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0234-2019·2018-10-31
Ecolab Recalls Da Vinci Robotic System Disposable Accessory Kits
Ecolab is recalling specific lots of Disposable Accessory Kits for the Da Vinci Si Robotic system because wrinkles in the packaging seal could compromise sterility.
Product
Disposable Accessory Kit, 4-Arm (Box of 5) individually sealed in poly-Tyvek pouches / Rx Sterile / to used exclusively on the Intuitive Surgical Da Vinci Si Robotic system / Distributed by Intuitive Surgical Product Usage: Microtek Medical Equipment Drapes are intended to…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·18V771000·2018-10-31
Kia Recalls 2019 Forte Vehicles for Headlight Aiming Defect
Kia is recalling 2019 Forte vehicles with LED headlights because they may not be aimed correctly, potentially reducing driver visibility and increasing crash risk.
Product
KIA — KIA FORTE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0206-2019·2018-10-31
ESAOTE MyLab Seven Ultrasound System Recalled for Probe Overheating Risk
ESAOTE is recalling 10 MyLab Seven ultrasound systems because probe power monitoring settings may cause the probe head to overheat during continuous operation.
Product
MyLab Seven, Model 6400
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0199-2019·2018-10-31
Canon MRI Systems Recall Due to SAR Display Error
Canon Medical System is recalling 252 MRI systems because the displayed SAR value may be lower than the actual value, potentially exceeding safety limits.
Product
Nuclear Magnetic Resonance Imaging Systems that are indicated for use as a diagnostic imaging modality that produces cross-sectional transaxial, coronal, sagittal, and oblique images that display anatomic structures of the head or body.
Category
Medical Device
Distribution
41 states
HighFDA (Devices)·Z-0232-2019·2018-10-31
Ecolab Camera Arm Drapes Recalled for Potential Sterility Breach
Ecolab is recalling specific lots of Camera Arm Drapes because wrinkles in the packaging seal could compromise the product's sterility.
Product
Camera Arm Drape (Box of 20) individually sealed in poly-Tyvek pouches / Rx Sterile / to used exclusively on the Intuitive Surgical Da Vinci Si Robotic system / Distributed by Intuitive Surgical Product Usage: Microtek Medical Equipment Drapes are intended to cover/wrap…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0273-2019·2018-10-31
Medtronic Recalls O-arm 1000 2nd Edition Imaging Systems for Software Anomalies
Medtronic is recalling 596 O-arm 1000 2nd Edition Imaging Systems worldwide due to software anomalies affecting startup, communication, and imaging functions.
Product
O-arm 1000 2nd Edition Imaging System, BASE OARM Bl70000027100 SYSTEM lOOV, Model Number Bl70000027100 Product Usage: The O-arm Imaging System is a mobile x-ray system designed for 2D fluoroscopic and 3D imaging and is intended to be used where a physician benefits from 2D…
Category
Medical Device
Distribution
45 states
HighFDA (Devices)·Z-0213-2019·2018-10-31
Siemens APTIO 9000 Refrigerated Storage Module Recall for Missing Warning Label
Siemens Healthcare Diagnostics is recalling 441 APTIO 9000 Refrigerated Storage Modules because they may have been shipped without a warning label regarding potential interference with pacemaker functionality.
Product
APTIO 9000 REFRIGERATED STORAGE MODULE
Category
Medical Device
Distribution
38 states
HighFDA (Devices)·Z-0211-2019·2018-10-31
Siemens APTIO Centrifuge Module Recall for Missing Pacemaker Warning Label
Siemens is recalling 441 APTIO Centrifuge Modules because they may have been shipped without a warning label regarding potential interference with pacemaker functionality.
Product
APTIO CENTRIFUGE MODULE
Category
Medical Device
Distribution
38 states
HighFDA (Devices)·Z-0271-2019·2018-10-31
Medtronic Recalls O-arm 1000 2nd Edition Imaging Systems Due to Software Anomalies
Medtronic is recalling 596 O-arm 1000 2nd Edition Imaging Systems worldwide due to reported software anomalies affecting startup, communication, and imaging functions.
Product
O-arm 1000 2nd Edition Imaging System, OARM ASSY Bl70000027 SYSTEM PRODUCT, Model Number Bl70000027 Product Usage: The O-arm Imaging System is a mobile x-ray system designed for 2D fluoroscopic and 3D imaging and is intended to be used where a physician benefits from 2D and…
Category
Medical Device
Distribution
45 states
HighFDA (Devices)·Z-0217-2019·2018-10-31
Siemens StreamLab Refrigerated Storage Module Recall for Missing Warning Label
Siemens is recalling StreamLab Refrigerated Storage Modules because they may lack a warning label regarding potential interference with pacemaker functionality.
Product
STREAMLAB - REFRIGERATED STORAGE MODULE 15000
Category
Medical Device
Distribution
38 states
HighFDA (Devices)·Z-0209-2019·2018-10-31
Siemens APTIO Input/Output Modules Recalled for Missing Pacemaker Warning Label
Siemens Healthcare Diagnostics is recalling 441 APTIO Input/Output Modules because they may have been shipped without a warning label regarding potential interference with pacemaker functionality.
Product
APTIO INPUT/OUTPUT MODULE
Category
Medical Device
Distribution
38 states
HighFDA (Devices)·Z-0280-2019·2018-10-31
Medtronic Recalls O-arm 1000 2nd Edition Imaging Systems Due to Software Anomalies
Medtronic is recalling 596 O-arm 1000 2nd Edition Imaging Systems worldwide due to reported software anomalies affecting startup, motion control, and image acquisition.
Product
O-arm 1000 2nd Edition Imaging System, OARM ASSY Bl70000027GERR SYS PRODUCT REFURB, Model Number Bl70000027GERR Product Usage: The O-arm Imaging System is a mobile x-ray system designed for 2D fluoroscopic and 3D imaging and is intended to be used where a physician benefits…
Category
Medical Device
Distribution
45 states