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. 2,457 recalls have been distributed to Alabama in the last 12 months.

50,591 total recalls
2,457 in last 12 months

Showing 3490134920 of 50,591 recalls

Medical DeviceMarch 25, 2016· Becton Dickinson & Company

Recalled Item: Henry Schein Single Use Syringe Luer-Lock Recalled by Becton Dickinson &...

The Issue: BD 10 mL Syringe Luer-Lok Tip with BD PrecisionGlide Needle 21G x 1 (0.8 mm...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance BigBore Oncology Computed Tomography X-ray systems Recalled by...

The Issue: Software defect causing intermittently slow response of Host.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· Abbott Laboratories

Recalled Item: CELL-DYN Emerald Cleaner Recalled by Abbott Laboratories Due to Three lots...

The Issue: Three lots of CELL-DYN Emerald Cleaner may have occurrences where the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance CT 16 Power Computed Tomography X-ray systems is intended...

The Issue: Software defect causing intermittently slow response of Host.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· Siemens Healthcare Diagnostics Inc.

Recalled Item: Dimension Vista 1500 Intelligent Lab System running on software versions...

The Issue: Discrepant patient results on Dimension Vista Intelligent Lab Systems....

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· Teleflex Medical

Recalled Item: Weck EFx Classic Fascial Closure System Recalled by Teleflex Medical Due to...

The Issue: Incorrect expiration date was printed on the product label.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 16 Computed Tomography X-ray systems is intended to produce...

The Issue: Software defect causing intermittently slow response of Host.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 64 Computed Tomography X-ray systems is intended to produce...

The Issue: Software defect causing intermittently slow response of Host.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· CareFusion 303, Inc.

Recalled Item: Alaris PC unit Recalled by CareFusion 303, Inc. Due to The Alaris PC units...

The Issue: The Alaris PC units model 8015 may display a system error code 133.6080 due...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance BigBore Radiology Computed Tomography X-ray systems Recalled by...

The Issue: Software defect causing intermittently slow response of Host.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core Computed Tomography X-ray systems is intended to produce...

The Issue: Software defect causing intermittently slow response of Host.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· Abbott Laboratories

Recalled Item: The ARCHITECT Estradiol Kit Intended to measure estradiol Recalled by Abbott...

The Issue: Interaction of Fulvestrant with the ARCHITECT Estradiol assay, leading to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core 128 Computed Tomography X-ray systems is intended to Recalled...

The Issue: Software defect causing intermittently slow response of Host.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· Siemens Healthcare Diagnostics Inc.

Recalled Item: Dimension Vista 500 Intelligent Lab System running on software versions...

The Issue: Discrepant patient results on Dimension Vista Intelligent Lab Systems....

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

Class II — Potential Health HazardOngoing
FoodMarch 24, 2016· Nestle Infant Nutrition

Recalled Item: GERBER Organic 2ND FOODS Pears Recalled by Nestle Infant Nutrition Due to...

The Issue: Gerber is voluntarily recalling two batches of GERBER¿ Organic 2ND FOODS¿...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodMarch 24, 2016· Nestle Infant Nutrition

Recalled Item: GERBER Organic 2ND FOODS¿ Carrots Recalled by Nestle Infant Nutrition Due to...

The Issue: Gerber is voluntarily recalling two batches of GERBER¿ Organic 2ND FOODS¿...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 24, 2016· AbbVie Inc.

Recalled Item: Zemplar (paricalcitol) capsules Recalled by AbbVie Inc. Due to Failed...

The Issue: Failed Content Uniformity Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugMarch 24, 2016· Lupin Limited

Recalled Item: Escitalopram Tablets USP 20 mg Recalled by Lupin Limited Due to Labeling:...

The Issue: Labeling: Incorrect or Missing Lot and/or Expiration Date

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugMarch 23, 2016· Akorn, Inc.

Recalled Item: ORIS (chlorhexidine gluconate) Recalled by Akorn, Inc. Due to Failed...

The Issue: Failed impurities/degradation specifications: Out-of-specification result...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 23, 2016· Hospira Inc.

Recalled Item: Magnesium Sulfate Inj. Recalled by Hospira Inc. Due to Failed pH...

The Issue: Failed pH Specifications: Confirmed high out of specification (OOS) results...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund