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. 1,056 recalls have been distributed to Alabama in the last 12 months.

50,591 total recalls
1,056 in last 12 months

Showing 17521–17540 of 50,591 recalls

Medical DeviceSeptember 24, 2020· Zimmer Biomet, Inc.

Recalled Item: ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene Recalled by...

The Issue: Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2020· Zimmer Biomet, Inc.

Recalled Item: ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene Recalled by...

The Issue: Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2020· Zimmer Biomet, Inc.

Recalled Item: ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene Recalled by...

The Issue: Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2020· Zimmer Biomet, Inc.

Recalled Item: ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene Recalled by...

The Issue: Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2020· Zimmer Biomet, Inc.

Recalled Item: ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene Recalled by...

The Issue: Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2020· Zimmer Biomet, Inc.

Recalled Item: ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene Recalled by...

The Issue: Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2020· Zimmer Biomet, Inc.

Recalled Item: ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene Recalled by...

The Issue: Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2020· Zimmer Biomet, Inc.

Recalled Item: ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene Recalled by...

The Issue: Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2020· Zimmer Biomet, Inc.

Recalled Item: ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene Recalled by...

The Issue: Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis...

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

Class II — Potential Health HazardOngoing
DrugSeptember 23, 2020· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: RIOMET ER (metformin hydrochloride for extended-release oral suspension)...

The Issue: CGMP Deviations: Detection of N-nitrosodimethylamine (NDMA) impurity in...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 22, 2020· Pentax of America Inc

Recalled Item: 9372HD Digital Capture (ver. 1.1.0 + w/ 9263 endoPortal) Recalled by Pentax...

The Issue: There is an intermittent software issue that could affect the systems, in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2020· Gordian Surgical

Recalled Item: TroClose 1200 - Product Usage: intended for use in a variety of gynecologic...

The Issue: Endotoxin test results found above the acceptable levels in LAL test (above...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2020· Cardinal Health 200, LLC

Recalled Item: Kangaroo Connect 1000ml Bag Set Recalled by Cardinal Health 200, LLC Due to...

The Issue: The feeding spike sets may leak at the interface of the tube and spike...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2020· Boston Scientific Corporation

Recalled Item: Visual-ICE MRI Cryoablation System Mobile Connection Panel (Visual-ICE MRI...

The Issue: Incorrectly installed base.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2020· Flexicare Medical Ltd.

Recalled Item: ProVu Single Use Video Stylet with ET Tube Recalled by Flexicare Medical...

The Issue: When the video stylet cuff is over-inflated there is potential for occlusion...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 22, 2020· Pentax of America Inc

Recalled Item: 9310HD Digital Video Capture Module with software version 3.4.0 or Recalled...

The Issue: There is an intermittent software issue that could affect the systems, in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2020· Cardinal Health 200, LLC

Recalled Item: Kangaroo Connect 500ml Bag Set Recalled by Cardinal Health 200, LLC Due to...

The Issue: The feeding spike sets may leak at the interface of the tube and spike...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2020· Stryker Neurovascular

Recalled Item: Trevo XP ProVue Retriever Recalled by Stryker Neurovascular Due to Increase...

The Issue: Increase in fracture complaints of the flexible, tapered core wire,...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 21, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Artis one systems with a Display Port transceiver-Fluoroscopic X-Ray...

The Issue: Potential malfunction in which the examination room monitor may become...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2020· Smith & Nephew, Inc.

Recalled Item: Genesis (GII) - Product Usage: designed for use in patients Recalled by...

The Issue: The anterior locking detail does not meet its design specifications.

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

Class II — Potential Health HazardOngoing