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. 2,708 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,708 in last 12 months

Showing 2152121540 of 55,713 recalls

DrugNovember 11, 2019· AuroMedics Pharma LLC

Recalled Item: Amiodarone Hydrochloride Injection Recalled by AuroMedics Pharma LLC Due to...

The Issue: Crystallization: Presence of visible particulate matter.

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

Class III — Low RiskOngoing
Refund
DrugNovember 11, 2019· AuroMedics Pharma LLC

Recalled Item: Amiodarone Hydrochloride Injection Recalled by AuroMedics Pharma LLC Due to...

The Issue: Crystallization: Presence of visible particulate matter.

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

Class III — Low RiskOngoing
Refund
DrugNovember 11, 2019· AuroMedics Pharma LLC

Recalled Item: Lidocaine HCl Injection Recalled by AuroMedics Pharma LLC Due to Foreign...

The Issue: Presence of Foreign Substance: Foreign material found inside the vial.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 11, 2019· AuroMedics Pharma LLC

Recalled Item: Amiodarone Hydrochloride Injection Recalled by AuroMedics Pharma LLC Due to...

The Issue: Crystallization: Presence of visible particulate matter.

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

Class III — Low RiskOngoing
Refund
FoodNovember 11, 2019· Kettle Cuisine, LLC

Recalled Item: Marketside Creamy Cauliflower Parmesan Soup 16 ounce Codes: 8113130606...

The Issue: Soup labeled Creamy Cauliflower Parmesan Soup may contain undeclared fish...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 11, 2019· Nextremity Solutions

Recalled Item: Stratum MDS Screw 3.5x46mm ST Part Number: STRM-MDS-3546ST Recalled by...

The Issue: Components 2mm shorter than indicated on the package label

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2019· Abbott Medical

Recalled Item: CLASSIC Radiofrequency Cannula - Curved Recalled by Abbott Medical Due to A...

The Issue: A manufacturing error caused a single lot of 10mm active tip length Cannulas...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2019· Smith & Nephew, Inc.

Recalled Item: smith&nephew PROFIX Mallet Recalled by Smith & Nephew, Inc. Due to There is...

The Issue: There is a a potential failure mode associated with the use of the mallet,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2019· Nextremity Solutions

Recalled Item: Stratum MDS Screw 3.5x50mm ST Part Number: STRM-MDS-3550ST Recalled by...

The Issue: Components 2mm shorter than indicated on the package label

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2019· Nextremity Solutions

Recalled Item: Stratum MDS Screw 3.5x48mm ST Part Number: STRM-MDS-3548ST Recalled by...

The Issue: Components 2mm shorter than indicated on the package label

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2019· Boston Scientific Corporation

Recalled Item: AngioJet Ultra Consoles-Thrombectomy System UPN: 105650-001D 105650-001H...

The Issue: Missing Directions for Use (DFU) - Consoles shipped to customers without the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2019· Cook Inc.

Recalled Item: CrossCath Support Catheter Recalled by Cook Inc. Due to A manufacturing...

The Issue: A manufacturing error may cause the radiopaque marker bands to be too loose...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 8, 2019· Cook Inc.

Recalled Item: CrossCath Support Catheter Recalled by Cook Inc. Due to A manufacturing...

The Issue: A manufacturing error may cause the radiopaque marker bands to be too loose...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 8, 2019· Cook Inc.

Recalled Item: CrossCath Support Catheter Recalled by Cook Inc. Due to A manufacturing...

The Issue: A manufacturing error may cause the radiopaque marker bands to be too loose...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 8, 2019· Cook Inc.

Recalled Item: CrossCath Support Catheter Recalled by Cook Inc. Due to A manufacturing...

The Issue: A manufacturing error may cause the radiopaque marker bands to be too loose...

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

Class I — Serious Health HazardOngoing
DrugNovember 8, 2019· Washington Homeopathic Products, Inc.

Recalled Item: StellaLife VEGA Oral Gel Rinse (In equal parts of: Azadirachta Indica 1x...

The Issue: CGMP Deviations: products were not manufactured under current good...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 8, 2019· Washington Homeopathic Products, Inc.

Recalled Item: Cell Salts Combination 6X Tablets Recalled by Washington Homeopathic...

The Issue: CGMP Deviations: products were not manufactured under current good...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 8, 2019· Washington Homeopathic Products, Inc.

Recalled Item: R2103 Recalled by Washington Homeopathic Products, Inc. Due to CGMP...

The Issue: CGMP Deviations: products were not manufactured under current good...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 8, 2019· Washington Homeopathic Products, Inc.

Recalled Item: Magnesia Phosphorica 6X Tablets Recalled by Washington Homeopathic Products,...

The Issue: CGMP Deviations: products were not manufactured under current good...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 8, 2019· Washington Homeopathic Products, Inc.

Recalled Item: Kali Muriaticum 6X Tablets Recalled by Washington Homeopathic Products, Inc....

The Issue: CGMP Deviations: products were not manufactured under current good...

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

Class II — Potential Health HazardOngoing
Refund