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. 2,442 recalls have been distributed to Alabama in the last 12 months.

50,591 total recalls
2,442 in last 12 months

Showing 3784137860 of 50,591 recalls

Medical DeviceJuly 1, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: GEMINI TF Ready CT/PET System. The Philips GEMINI PET/CT Imaging Recalled by...

The Issue: Philips has identified four (4) software defects in the Tumor LOC software...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: GEMINI LXL CT/PET System. The Philips GEMINI PET/CT Imaging Systems Recalled...

The Issue: Philips has identified four (4) software defects in the Tumor LOC software...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/ zeego systems Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: in case a system error occurs and the system enters the "Bypass Fluoro" mode...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2015· Remel Inc

Recalled Item: PathoDx Strep B Grouping Latex Recalled by Remel Inc Due to A reagent...

The Issue: A reagent present may produce weak or slow reactions; continued use may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2015· BIOTRONIK, Inc.

Recalled Item: PSW 1203.U/1 Recalled by BIOTRONIK, Inc. Due to Ventricular packing: LV...

The Issue: Ventricular packing: LV software programming versions for BIOTRONIK CRT-P...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2015· Remel Inc

Recalled Item: PathoDx Strep Grouping Kit Recalled by Remel Inc Due to A reagent present...

The Issue: A reagent present may produce weak or slow reactions; continued use may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2015· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Chemistry Acetaminophen reagents Recalled by Siemens Healthcare...

The Issue: A change in the concentration of N-acetylcysteine (NAC) that may cause...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2015· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to Software anomaly may...

The Issue: Software anomaly may occur during the installation of an Assay Data Diskette...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2015· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Fujinon/Fujifilm Processor EPX 2500 Operation Manual. For use in endoscopic...

The Issue: The EPX-2500 Operation Manual and sales brochure incorrectly identify that...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2015· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Fujifilm Processor EPX 2500 High Definition Endoscopy Recalled by Fujifilm...

The Issue: The EPX-2500 Operation Manual and sales brochure incorrectly identify that...

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

Class II — Potential Health HazardOngoing
FoodJune 30, 2015· Michael Foods, Inc.

Recalled Item: Crystal Farms Simply Potatoes Shredded Hash Browns packaged as individual...

The Issue: Product may contain small slivers of shredded golf ball.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 30, 2015· Hospira Inc.

Recalled Item: KETOROLAC Tromethamine Inj. Recalled by Hospira Inc. Due to Crystallization;...

The Issue: Crystallization; identified as calcium salt of Ketorolac

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 30, 2015· Hospira Inc.

Recalled Item: KETOROLAC Tromethamine Inj. Recalled by Hospira Inc. Due to Crystallization;...

The Issue: Crystallization; identified as calcium salt of Ketorolac

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 30, 2015· Mylan Pharmaceuticals Inc

Recalled Item: Capecitabine Tablets Recalled by Mylan Pharmaceuticals Inc Due to Failed...

The Issue: Failed Dissolution Specifications: low out-of-specification (OOS) results...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 29, 2015· Qualitest Pharmaceuticals

Recalled Item: HydrOXYzine Hydrochloride Tablets Recalled by Qualitest Pharmaceuticals Due...

The Issue: Failed Tablet/Capsule Specifications; The identification codes on some...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 29, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Artis zee systems Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: The possibility exists for a large amount of liquid to seep through the top...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2015· Covidien LP (formerly Nellcor Puritan Bennett Inc.)

Recalled Item: OxiMax N-560 Pulse Oximeter. For continuous or spot check monitoring...

The Issue: Potential missing segments on the display that can result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q systems Recalled by Siemens Medical Solutions USA, Inc Due to The...

The Issue: The possibility exists for a large amount of liquid to seep through the top...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2015· Covidien LP (formerly Nellcor Puritan Bennett Inc.)

Recalled Item: OxiMax N-65 Handheld Pulse Oximeter. N65 Recalled by Covidien LP (formerly...

The Issue: Potential missing segments on the display that can result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: Axiom Artis systems Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: The possibility exists for a large amount of liquid to seep through the top...

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

Class II — Potential Health HazardOngoing