Product Recalls in Texas

Product recalls affecting Texas — including food, drugs, consumer products, medical devices, and vehicles distributed to Texas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,692 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,692 in last 12 months

Showing 2142121440 of 30,921 recalls

Medical DeviceJuly 7, 2016· Siemens Medical Solutions USA, Inc

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

The Issue: Due to an error in the 19 Live Display, image reproduction may fail in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2016· Bard Peripheral Vascular Inc

Recalled Item: Bard TruGuide Disposable Coaxial Biopsy Needle  Mixed Product Part Recalled...

The Issue: May contain two trocar tip stylets with coaxials or two blunt tip stylets...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2016· Smith & Nephew, Inc.

Recalled Item: SPHERICAL HEAD (R) 6.5 MM CANCELLOUS SCREW Recalled by Smith & Nephew, Inc....

The Issue: The labels correctly state that the product should be a 25mm screw, but the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 5, 2016· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDPoint¿ 500 v2.2.2A Software Upgrade Kit Recalled by Siemens...

The Issue: Some v2.2.2 upgrade kits include a dialysate mode which not cleared/approved...

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

Class III — Low RiskOngoing
Medical DeviceJuly 5, 2016· Implant Direct Sybron Manufacturing, LLC

Recalled Item: RePlant¿ Angled Abutment Part Number 6050-52-60 Recalled by Implant Direct...

The Issue: Issue with design specification; oversized condition.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 5, 2016· Branan Medical Corporation

Recalled Item: AmediCheck Instant Test Cup Recalled by Branan Medical Corporation Due to...

The Issue: Branan Medical is recalling the AmediCheck Instant Test Cup, a 5 panel drug...

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

Class III — Low RiskOngoing
Medical DeviceJuly 4, 2016· Zimmer Surgical Inc

Recalled Item: Zimmer¿ Air Dermatome II Handpiece Loaner Recalled by Zimmer Surgical Inc...

The Issue: Zimmer Biomet Surgical has received product complaints reporting that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2016· Zimmer Surgical Inc

Recalled Item: Zimmer¿ Air Dermatome II Handpiece w/o Hose Recalled by Zimmer Surgical Inc...

The Issue: The surface coating applied to the device is blistering, peeling and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2016· Zimmer Surgical Inc

Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...

The Issue: The surface coating applied to the device is blistering, peeling and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2016· Zimmer Surgical Inc

Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...

The Issue: The surface coating applied to the device is blistering, peeling and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2016· Zimmer Surgical Inc

Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...

The Issue: The surface coating applied to the device is blistering, peeling and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2016· Zimmer Surgical Inc

Recalled Item: Zimmer¿ Air Dermatome II Handpiece Recalled by Zimmer Surgical Inc Due to...

The Issue: The surface coating applied to the device is blistering, peeling and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2016· Zimmer Surgical Inc

Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...

The Issue: The surface coating applied to the device is blistering, peeling and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2016· Zimmer Surgical Inc

Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...

The Issue: The surface coating applied to the device is blistering, peeling and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2016· Mentor Texas, LP.

Recalled Item: Mentor MemoryGel Breast Implant Recalled by Mentor Texas, LP. Due to The box...

The Issue: The box of 300cc MemoryGel Breast Implant was labeled with null...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2016· Sysmex America Inc

Recalled Item: Fluorocell PLT reagent Recalled by Sysmex America Inc Due to There is a...

The Issue: There is a potential that fluorescent platelet (PLT-F) and immature platelet...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Orthopedic manual surgical instrument Usage: Exeter Rasp Handle is a...

The Issue: Malfunctioning of the Exeter Rasp/trial introducer/extractor Handle.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2016· Circulatory Technology Inc

Recalled Item: The Bigger-Better-Bladder Recalled by Circulatory Technology Inc Due to The...

The Issue: The seal between the balloon and the housing may leak.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2016· Nidek Inc

Recalled Item: OPTICAL BIOMETER AL-Scan: Software Version: 1.09 and earlier. Ophthalmic:...

The Issue: Nidek Inc. received information from our manufacturer NIDEK CO. Japan that...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2016· Circulatory Technology Inc

Recalled Item: The Better-Bladder With 14" ID tubing Recalled by Circulatory Technology Inc...

The Issue: Twisted or wrinkled balloon components which are considered a cosmetic...

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

Class III — Low RiskOngoing