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 2524125260 of 28,641 recalls

Medical DeviceNovember 25, 2013· Carestream Health, Inc.

Recalled Item: DRX-Evolution with FF WS These products are permanently installed diagnostic...

The Issue: Carestream Health Inc. has issued a recall for the Carestream DRX-Evolution...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2013· Abbott Vascular, Inc.

Recalled Item: HT Connect Peripheral Guide Wire Part Number Description 1012587 018...

The Issue: Abbott Vascular has initiated a recall of the HT Connect Peripheral Guide...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2013· C.L.R. Medicals International, Inc.

Recalled Item: Viscocel and Viscocel Plus. These products are intraocular fluid devices...

The Issue: CLR Medicals International Inc., initiated a nationwide recall of Viscocel...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 25, 2013· Roche Diagnostics Operations, Inc.

Recalled Item: MagNA Pure 96 System Version 1.0 Software Version 2.0 Robotic Recalled by...

The Issue: This issue is only relevant for customers importing xml files into the MagNA...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

Recalled Item: G1469J: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue...

The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

Recalled Item: 4042LH: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue...

The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Bio-Rad Laboratories, Inc.

Recalled Item: D-10 Dual Program Recalled by Bio-Rad Laboratories, Inc. Due to D-10 A1c...

The Issue: D-10 A1c Dual Program Floppy was programmed incorrectly and cartridge...

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

Class III — Low RiskOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

Recalled Item: G1725: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue with...

The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

Recalled Item: G1762: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue with...

The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

Recalled Item: 4043-2: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue...

The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

Recalled Item: 4042E: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue with...

The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

Recalled Item: 4043W-2: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue...

The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

Recalled Item: 4043E: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue with...

The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

Recalled Item: 4040-2: Umbilical 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to...

The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

Recalled Item: 4043G-2: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue...

The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

Recalled Item: Medfusion¿ 4000 Syringe Infusion Pumps Medfusion¿ 4000 Syringe Infusion...

The Issue: Smiths Medical is conducting a recall involving all Medfusion¿ 4000 Syringe...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

Recalled Item: G2001: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue with...

The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

Recalled Item: G1777: Umbilical (2) 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due...

The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

Recalled Item: 4042-2: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue...

The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2013· Horiba Instruments, Inc dba Horiba Medical

Recalled Item: ABX PENTRA N Control Recalled by Horiba Instruments, Inc dba Horiba Medical...

The Issue: Horiba Medical is recalling the ABX PENTRA N Control because it has been...

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

Class II — Potential Health HazardOngoing