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 3502135040 of 50,591 recalls

Medical DeviceMarch 14, 2016· Terumo Cardiovascular Systems Corporation

Recalled Item: CDI Blood Parameter Monitoring System 500 Cardiopulmonary bypass on-line...

The Issue: Specific CDI¿ Blood Parameter Monitoring System 500 devices are being...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Navilyst Medical, Inc., an AngioDyamics Company

Recalled Item: BioFlo PICC with ENDEXO and PASV Valve Technology Recalled by Navilyst...

The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Navilyst Medical, Inc., an AngioDyamics Company

Recalled Item: Xcela PICC with PASV Valve Technology Catheter Kit Recalled by Navilyst...

The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Navilyst Medical, Inc., an AngioDyamics Company

Recalled Item: BioFlo PICC with ENDEXO and PASV Valve Technology Recalled by Navilyst...

The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Navilyst Medical, Inc., an AngioDyamics Company

Recalled Item: BioFlo PICC with ENDEXO and PASV Valve Technology Recalled by Navilyst...

The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Navilyst Medical, Inc., an AngioDyamics Company

Recalled Item: Vaxcel PICC with PASV MST-60 Kit under the following labels: 1) 3F Recalled...

The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Navilyst Medical, Inc., an AngioDyamics Company

Recalled Item: Xcela PICC with PASV Valve Technology Recalled by Navilyst Medical, Inc., an...

The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Navilyst Medical, Inc., an AngioDyamics Company

Recalled Item: Vaxcel PICC with PASV Intermediate Safety MST Kit under the Recalled by...

The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2016· RESEARCH INSTRUMENTS LTD - SITE B

Recalled Item: Integra 3 Recalled by RESEARCH INSTRUMENTS LTD - SITE B Due to The units...

The Issue: The units have been fitted with a potentially faulty power supply cable.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2016· Integra York PA, Inc

Recalled Item: Miltex Premium Grade Self-Lock Chisel Blade Handle Recalled by Integra York...

The Issue: One lot of self-lock chisel blade handles have a wider slot that holds the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2016· Integra LifeSciences Corporation

Recalled Item: Integra Meshed Dermal Regeneration Template 5 cmx 5 cm (2 Recalled by...

The Issue: Integra's post QA release review of historical product release test results...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Artis One Recalled by Siemens Medical Solutions USA, Inc Due to After...

The Issue: After importing segmentation results of the left atrium created on the Artis...

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

Class II — Potential Health HazardOngoing
DrugMarch 11, 2016· Lupin Pharmaceuticals Inc.

Recalled Item: Ceftriaxone for Injection USP Recalled by Lupin Pharmaceuticals Inc. Due to...

The Issue: CGMP Deviations: finished products manufactured using active pharmaceutical...

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

Class III — Low RiskOngoing
Refund
DrugMarch 11, 2016· Jubilant Draximage Inc

Recalled Item: SODIUM IODIDE I 131 CAPSULE Recalled by Jubilant Draximage Inc Due to...

The Issue: Labeling: Label Error on Declared Strength

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

Class III — Low RiskOngoing
Refund
DrugMarch 11, 2016· Lupin Pharmaceuticals Inc.

Recalled Item: Ceftriaxone for Injection USP Recalled by Lupin Pharmaceuticals Inc. Due to...

The Issue: CGMP Deviations: finished products manufactured using active pharmaceutical...

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

Class III — Low RiskOngoing
Refund
DrugMarch 11, 2016· Lupin Pharmaceuticals Inc.

Recalled Item: Ceftriaxone for Injection USP Recalled by Lupin Pharmaceuticals Inc. Due to...

The Issue: CGMP Deviations: finished products manufactured using active pharmaceutical...

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

Class III — Low RiskOngoing
Refund
DrugMarch 11, 2016· Lupin Pharmaceuticals Inc.

Recalled Item: Ceftriaxone for Injection USP Recalled by Lupin Pharmaceuticals Inc. Due to...

The Issue: CGMP Deviations: finished products manufactured using active pharmaceutical...

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

Class III — Low RiskOngoing
Refund
DrugMarch 11, 2016· Lupin Pharmaceuticals Inc.

Recalled Item: Ceftriaxone Sodium (Sterile) USP active pharmaceutical ingredient Recalled...

The Issue: CGMP Deviations: active pharmaceutical ingredient intermediates failed...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 11, 2016· Datascope Corporation

Recalled Item: Maquet Cardiopulmonary Bypass Custom Tubing kit BEQ-T 5208 ECC SET Recalled...

The Issue: There is a potential problem with the cuvette where failure of the cuvette...

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

Class III — Low RiskOngoing
Medical DeviceMarch 11, 2016· Datascope Corporation

Recalled Item: Maquet Cardiopulmonary Bypass Custom Tubing kit BEQ-TOP 5909 14 Pack QPID...

The Issue: There is a potential problem with the cuvette where failure of the cuvette...

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

Class III — Low RiskOngoing