Product Recalls in Alabama

Product recalls affecting Alabama — including food, drugs, consumer products, medical devices, and vehicles distributed to Alabama. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,467 recalls have been distributed to Alabama in the last 12 months.

50,591 total recalls
2,467 in last 12 months

Showing 2706127080 of 28,641 recalls

Medical DeviceDecember 20, 2012· Medisystems a NX Stage Company

Recalled Item: Medisystems 17 Gauge x 1" inch AV Fistula Needle Product Recalled by...

The Issue: Single needle packs in each case ( 10 needles per case) are mislabeled on...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2012· Carefusion 303 Inc

Recalled Item: CareFusion SmartSite Gravity Blood Set Model 42082E. Used to administer...

The Issue: CareFusion is recalling the SmartSite¿ Gravity Blood Set as a result of a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2012· Abbott Medical Optics Inc (AMO)

Recalled Item: AMO Sensar Intraocular Lenses (IOLs) Recalled by Abbott Medical Optics Inc...

The Issue: Two production orders of these IOLs that contain mislabeled IOLs.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2012· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Total Iron Binding Capacity (IBCT) Flex Reagent Cartridge. An...

The Issue: The analytical sensitivity claim of 6 ug/dL (1.1 umol/L) in the Instructions...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceDecember 20, 2012· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 6 Recalled by Philips Medical Systems (Cleveland) Inc Due to...

The Issue: Philips Healthcare received reports from the field stating the patient table...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2012· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension(R) IRON Calibrator (DC85) Recalled by Siemens Healthcare...

The Issue: Siemens Healthcare Diagnostics has received complaints of IRON calibrations...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceDecember 19, 2012· Elekta, Inc.

Recalled Item: Elekta Synergy XVI. Radiation Therapy Digital Imager. Product XVI R3.5.1...

The Issue: The DICOM tags do not contain sufficient information for XVI to identify the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2012· Philips Medical Systems (Cleveland) Inc

Recalled Item: Philips MX 16-Slice CT Scanner System Recalled by Philips Medical Systems...

The Issue: The four screws that secure the patient table top to the carrier became...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2012· Hamilton Medical Inc

Recalled Item: HAMILTON-T1 Ventilator with software versions 1.1.2 or lower. The HAMILTON...

The Issue: Analysis of a customer complaint has shown that during ventilation of small...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2012· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista (R) Urinary/Cerebrospinal Fluid Protein (UCFP) Flex (R)...

The Issue: Siemens has confirmed an increase on absorbance errors when calibrating...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2012· Leica Microsystems (Schweiz) Ag

Recalled Item: Surgical microscope The device is used to improve the visibility Recalled by...

The Issue: The brake in the Z axis and/or brakes in the AB and C axes failed during...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2012· Leica Microsystems (Schweiz) Ag

Recalled Item: Surgical microscope The device is used to improve the visibility Recalled by...

The Issue: The brake in the Z axis and/or brakes in the AB and C axes failed during...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2012· Cardinal Health

Recalled Item: Needle Counters with Blade Disarmer Recalled by Cardinal Health Due to Small...

The Issue: Small holes (approximately 1 mm or less) found in device unit level...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2012· Cardinal Health

Recalled Item: Needle Counters Recalled by Cardinal Health Due to Small holes...

The Issue: Small holes (approximately 1 mm or less) found in device unit level...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2012· Cardinal Health

Recalled Item: Needle Counters with Blade Disarmer Recalled by Cardinal Health Due to Small...

The Issue: Small holes (approximately 1 mm or less) found in device unit level...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2012· Cardinal Health

Recalled Item: Needle Counters Recalled by Cardinal Health Due to Small holes...

The Issue: Small holes (approximately 1 mm or less) found in device unit level...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2012· Cardinal Health

Recalled Item: Needle Counters Recalled by Cardinal Health Due to Small holes...

The Issue: Small holes (approximately 1 mm or less) found in device unit level...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2012· Cardinal Health

Recalled Item: Needle Counters with Blade Disarmer Recalled by Cardinal Health Due to Small...

The Issue: Small holes (approximately 1 mm or less) found in device unit level...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2012· Stryker Medical Division of Stryker Corporation

Recalled Item: Medical Surgical Bed Recalled by Stryker Medical Division of Stryker...

The Issue: Stryker Medical Model 3002S3EX and Model 3005S3EX beds built between March...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2012· Stryker Medical Division of Stryker Corporation

Recalled Item: Medical Surgical Bed Recalled by Stryker Medical Division of Stryker...

The Issue: Stryker Medical Model 3002S3EX and Model 3005S3EX beds built between March...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing