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 2924129260 of 50,591 recalls

Medical DeviceJune 12, 2017· Zimmer Biomet, Inc.

Recalled Item: DRILL BIT MINI QUICK CONNECT 1.0MM Recalled by Zimmer Biomet, Inc. Due to A...

The Issue: A raw material anomaly was discovered in four lots of raw material and has...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2017· Arrow International Inc

Recalled Item: Arrow EVOLUTION Pressure Injectable PICC with Chlorag+ard Antimicrobial and...

The Issue: Arrow is recalling additional lots that were identified as part of an active...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2017· Arrow International Inc

Recalled Item: Arrow Glide Thru Peel-Away Sheath/Dilator Introducer Recalled by Arrow...

The Issue: Arrow is recalling additional lots that were identified as part of an active...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2017· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek Aviva II Meter - Product Usage: a. The Accu-Chek Recalled by Roche...

The Issue: Meters may contain a damaged C29 capacitor resulting in issues with power...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2017· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek Performa II Meter - Product Usage: a. The Accu-Chek Recalled by...

The Issue: Meters may contain a damaged C29 capacitor resulting in issues with power...

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

Class II — Potential Health HazardOngoing
DrugJune 12, 2017· Vi-Jon, Inc.

Recalled Item: Magnesium Citrate Saline Laxative Cherry Flavored Recalled by Vi-Jon, Inc....

The Issue: Presence of foreign substance: glass particle

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 12, 2017· Sanofi-Aventis U.S. LLC

Recalled Item: Gaviscon (Alumina & Magnesium Trisilicate) Regular Strength Original Flavor...

The Issue: Superpotent Drug: high out-of-specification result for magnesium.

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 11, 2017· Tosoh Bioscience Inc

Recalled Item: Tosoh¿Automated Enzyme Immunoassay Analyzer AIA-900 Recalled by Tosoh...

The Issue: This recall has been initiated due to a potential malfunction of the photo...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2017· Tosoh Bioscience Inc

Recalled Item: Tosoh¿Sorter 9tray Recalled by Tosoh Bioscience Inc Due to This recall has...

The Issue: This recall has been initiated due to a potential malfunction of the photo...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2017· Kelyniam Global, Inc.

Recalled Item: Kelyniam Custom Skull Implant (CSI) Recalled by Kelyniam Global, Inc. Due to...

The Issue: Significant design changes made to the Custom Skull Implant (CSI) devices,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2017· Kelyniam Global, Inc.

Recalled Item: Kelyniam Custom Skull Implant (CSI) Recalled by Kelyniam Global, Inc. Due to...

The Issue: Significant design changes made to the Custom Skull Implant (CSI) devices,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2017· Kelyniam Global, Inc.

Recalled Item: Kelyniam Custom Skull Implant (CSI) Recalled by Kelyniam Global, Inc. Due to...

The Issue: Significant design changes made to the Custom Skull Implant (CSI) devices,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2017· Kelyniam Global, Inc.

Recalled Item: Kelyniam Custom Skull Implant (CSI) Recalled by Kelyniam Global, Inc. Due to...

The Issue: Significant design changes made to the Custom Skull Implant (CSI) devices,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2017· Sorin Group USA, Inc.

Recalled Item: Sorin Group Aortic Arch Cannula Recalled by Sorin Group USA, Inc. Due to...

The Issue: Identification of excess plastic on the tip of the cannula.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2017· Natus Neurology Inc

Recalled Item: Nicolet¿ Elite¿ 3 MHz OB Probe Recalled by Natus Neurology Inc Due to Some...

The Issue: Some of the Elite 2 and 3 Obstetric probes and 5 MHz Vascular Probes may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2017· Natus Neurology Inc

Recalled Item: Nicolet¿ Elite¿ 2 MHz OB Probe Recalled by Natus Neurology Inc Due to Some...

The Issue: Some of the Elite 2 and 3 Obstetric probes and 5 MHz Vascular Probes may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2017· Penumbra Inc.

Recalled Item: Penumbra 3D Revascularization Device It is indicated for used in Recalled by...

The Issue: Penumbra has identified an issue in these four lots involving a raw material...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 9, 2017· Natus Neurology Inc

Recalled Item: Nicolet¿ Elite¿ 2 MHz OB Water Proof Probe Recalled by Natus Neurology Inc...

The Issue: Some of the Elite 2 and 3 Obstetric probes and 5 MHz Vascular Probes may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2017· Natus Neurology Inc

Recalled Item: Nicolet¿ Elite¿ 5 MHz Vascular Probe Recalled by Natus Neurology Inc Due to...

The Issue: Some of the Elite 2 and 3 Obstetric probes and 5 MHz Vascular Probes may...

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

Class II — Potential Health HazardOngoing
DrugJune 9, 2017· Advanced Pharma Inc.

Recalled Item: NitroGlycerin (2 mg/10 mL in 5% Dextrose Inj Recalled by Advanced Pharma...

The Issue: Stability Data Does Not Support Expiry: lots do not have stability that...

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

Class II — Potential Health HazardOngoing
Refund