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 3472134740 of 50,591 recalls

Medical DeviceApril 6, 2016· Pentax Medical Company

Recalled Item: Gastroscope Product Usage: Intended to provide optical visualization of and...

The Issue: Pentax Medical Video Processor EPK-i5010 has been shipped with a reusable...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2016· Pentax Medical Company

Recalled Item: Duodenoscope Product Usage: Intended to provide optical visualization of and...

The Issue: Pentax Medical Video Processor EPK-i5010 has been shipped with a reusable...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2016· Pentax Medical Company

Recalled Item: Signmoidoscope Product Usage: Intended to provide optical visualization of...

The Issue: Pentax Medical Video Processor EPK-i5010 has been shipped with a reusable...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2016· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5600 Integrated System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Ortho Clinical Diagnostics confirmed a software timing anomaly in which the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2016· Ortho-Clinical Diagnostics

Recalled Item: VITROS 3600 Immunodiagnostic System Recalled by Ortho-Clinical Diagnostics...

The Issue: Ortho Clinical Diagnostics confirmed a software timing anomaly in which the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2016· Skytron, Div. The KMW Group, Inc

Recalled Item: EZ Slide Battery/line powered hydraulic table with removable leg section...

The Issue: The potential exists within the identified tables that incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2016· Pentax Medical Company

Recalled Item: Colonoscope Product Usage: Intended to provide optical visualization of and...

The Issue: Pentax Medical Video Processor EPK-i5010 has been shipped with a reusable...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2016· Pentax Medical Company

Recalled Item: Ultrasound Gastroscope Product Usage: Intended to provide optical...

The Issue: Pentax Medical Video Processor EPK-i5010 has been shipped with a reusable...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2016· Ceg Enterprises Llc

Recalled Item: Germ Terminator Recalled by Ceg Enterprises Llc Due to CEG Enterprises, LLC...

The Issue: CEG Enterprises, LLC is recalling Germ Terminator Toothbrush Sanitizer GT100...

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

Class II — Potential Health HazardOngoing
FoodApril 5, 2016· Empirical Laboratories, Incorporated

Recalled Item: Liposomal Magnesium Nutritional Supplement. 6 FL. OZ (180 ml) The Recalled...

The Issue: Empirical Labs is recalling Liposomal Magnesium because of the potential for...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 5, 2016· Fresenius Kabi USA, LLC

Recalled Item: Cisatracurium Besylate Injection Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Incorrect/ Undeclared Excipient: Firm is recalling product due to an...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 4, 2016· Lupin Pharmaceuticals Inc.

Recalled Item: Lisinopril & Hydrochlorothiazide Tables Recalled by Lupin Pharmaceuticals...

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
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: Merge Cardio software. The firm name on the label is Merge Healthcare...

The Issue: When taking measurements from images on the Cardio workstation or from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: iConnect Enterprise Archive (ICEA) software. iConnect Enterprise Archive is...

The Issue: The study is archived but cannot be opened in iConnect Access and cannot...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: Merge Cardio software. Recalled by Merge Healthcare, Inc. Due to Cardio...

The Issue: Cardio study list does not show STAT studies without .

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: iConnect Enterprise Archive software. Recalled by Merge Healthcare, Inc. Due...

The Issue: The versions allow images to be stored without pixel data, resulting in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Mesa Laboratories Inc

Recalled Item: ProSpore 4 mL Ampoule Biological indicator for steam sterilization Recalled...

The Issue: Product resistance has fallen outside of label claim within expiry.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: MasimoSET LNOP DCI adult SpO2 reusable sensor Recalled by Merge Healthcare,...

The Issue: Under certain conditions, the cables used with the Hemo system during a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: Merge Eye Care Systems Recalled by Merge Healthcare, Inc. Due to The system...

The Issue: The system will completely stop allowing the downloading or acquisition of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: MasimoSET LNOP DCIP pediatric/slender digit SpO2 reusable sensor Recalled by...

The Issue: Under certain conditions, the cables used with the Hemo system during a...

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

Class II — Potential Health HazardOngoing