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. 2,829 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,829 in last 12 months

Showing 1288112900 of 55,713 recalls

Medical DeviceMay 31, 2022· Synapse Biomedical Inc

Recalled Item: NeuRx Diaphragm Pacing System (NeuRx DPS) Recalled by Synapse Biomedical Inc...

The Issue: Firm has revised labeling to consistently call out storage conditions and...

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

Class III — Low RiskOngoing
Medical DeviceMay 31, 2022· Boston Scientific Corporation

Recalled Item: GreenLight HPSEA Laser Fibers Recalled by Boston Scientific Corporation Due...

The Issue: Several complaints were received for the affected lot; users received a...

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

Class III — Low RiskOngoing
Medical DeviceMay 31, 2022· Baxter Healthcare Corporation

Recalled Item: NaviCare Nurse Call/Voalte Nurse Call Recalled by Baxter Healthcare...

The Issue: An issue has been identified with Phillips (Emergin) and Longleaf non relay...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2022· Shanghai United Imaging Healthcare Co., Ltd.

Recalled Item: Positron Emission Tomography and Computed Tomography System Recalled by...

The Issue: The wireless VSM module of a mobile PET/CT system, operating in an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2022· Ossur Americas

Recalled Item: OSSUR VARIFLEX SUBA JUNIOR foot and ankle external prosthesis Recalled by...

The Issue: Due to receiving complaints related to broken (cracked) prosthetic foot with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2022· Medtronic Neuromodulation

Recalled Item: LEAD 3387S-40 STIMLOC DBS Recalled by Medtronic Neuromodulation Due to There...

The Issue: There are a small number of units of the DBS Lead with StimLoc kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2022· GE Healthcare, LLC

Recalled Item: GE Healthcare Avance CS2 Recalled by GE Healthcare, LLC Due to The base of...

The Issue: The base of the anesthesia system can have a crack and could potentially...

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

Class II — Potential Health HazardOngoing
DrugMay 26, 2022· Amazon.com, Inc.

Recalled Item: Artri Ajo King con Ortiga y Omega 3 tablets Recalled by Amazon.com, Inc. Due...

The Issue: Marketed Without An Approved NDA/ANDA: FDA laboratory analysis found the...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 26, 2022· Amazon.com, Inc.

Recalled Item: Ortiga mas Ajo Rey con Omega 3 Recalled by Amazon.com, Inc. Due to...

The Issue: Marketed Without An Approved NDA/ANDA: FDA laboratory analysis found the...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 26, 2022· Amazon.com, Inc.

Recalled Item: Artri King con Ortiga y Omega 3 tablets Recalled by Amazon.com, Inc. Due to...

The Issue: Marketed Without An Approved NDA/ANDA: FDA laboratory analysis found the...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 26, 2022· Albanese Confectionery Group, Inc.

Recalled Item: Rich s Milk Chocolate Giant Layered Peanut Butter and Cups Recalled by...

The Issue: Salmonella. Product made using recalled Jif peanut butter

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 26, 2022· Paragon 28, Inc.

Recalled Item: HammerTube Implant Recalled by Paragon 28, Inc. Due to Due to Titanium...

The Issue: Due to Titanium plasma coating not present implant.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2022· Ortho-Clinical Diagnostics, Inc.

Recalled Item: Anti-SARS-CoV-2 IgG Quantitative Reagent Pack- Intended for use on VITROS¿...

The Issue: On-Analyzer Stability (OAS) time, supported for 6 weeks; not 8 weeks as is...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2022· Olympus Corporation of the Americas

Recalled Item: SOLTIVE SuperPulsed Laser Fibers Recalled by Olympus Corporation of the...

The Issue: Device model and size for affected lots of Laser Fibers may be mismatched...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: SPS MEDICAL SUPPLY Crosstex International Sterilization Roll Sani-Roll...

The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...

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

Class III — Low RiskOngoing
Medical DeviceMay 25, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Absorbent dressings. a. DERMA SCIENCES Recalled by Mckesson Medical-Surgical...

The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...

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

Class III — Low RiskOngoing
Medical DeviceMay 25, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: DERMARITE INDUSTRIES SafeWash Saline Saline Wound Flush SafeWash 7.1 oz....

The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...

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

Class III — Low RiskOngoing
Medical DeviceMay 25, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: a. SporView Culture Set SporView Sterilization Biological Indicator Kit...

The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...

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

Class III — Low RiskOngoing
Medical DeviceMay 25, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: DERMARITE INDUSTRIES DermaCol 100 Collagen Powder DermaCol 100 Collagen 1...

The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...

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

Class III — Low RiskOngoing
Medical DeviceMay 25, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Skin markers: a. IZI MEDICAL PRODUCTS LLC Multi-Modality Markers SKIN...

The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...

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

Class III — Low RiskOngoing