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. 1,049 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
1,049 in last 12 months

Showing 31641–31660 of 55,713 recalls

Medical DeviceJune 7, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity CT (Model No. 728326) Recalled by Philips Medical Systems...

The Issue: It was reported that scanners running certain software versions provide...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance Big Bore Radiology CT (Model No. 728244) software version...

The Issue: It was reported that scanners running certain software versions provide...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: IQon Spectral CT (Model No. 728332) Recalled by Philips Medical Systems...

The Issue: It was reported that scanners running certain software versions provide...

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

Class II — Potential Health HazardOngoing
FoodJune 6, 2017· Morris J. Golombeck, Inc.

Recalled Item: BIRDS EYE CHILIES MJG # 8178 Recalled by Morris J. Golombeck, Inc. Due to...

The Issue: Product may contain peanuts

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 6, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Zee and Zeego Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Potential for liquid entry

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q and Q.Zen Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Potential for liquid entry

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2017· Draegar Medical Systems, Inc.

Recalled Item: Draeger Medical Systems Infinity Acute Care System (M540) Catalog Numbers:...

The Issue: Cockpits with revision index 06 or higher that contain 4GB RAM modules may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2017· Spectranetics Corporation

Recalled Item: Spectranetics Turbo-Elite Laser Atherectomy Catheter Peripheral Rapid...

The Issue: Potential for flouroscopially visible marker band at the tip of the Rapid...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: Axiom Artis Recalled by Siemens Medical Solutions USA, Inc Due to Potential...

The Issue: Potential for liquid entry

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

Class II — Potential Health HazardOngoing
DrugJune 6, 2017· Bausch & Lomb, Inc.

Recalled Item: NasalCrom (cromolyn sodium) Nasal Spray Recalled by Bausch & Lomb, Inc. Due...

The Issue: CGMP Deviations: Possibility of the presence of microbial contamination in...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 6, 2017· Microbiologics Inc

Recalled Item: Helix Elite" Molecular Standards: Inactivated Standard. Inactivated...

The Issue: Real-time shelf life testing failed at 24 months

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2017· Microbiologics Inc

Recalled Item: Helix Elite" Molecular Standards: Inactivated Standard. Inactivated...

The Issue: Real-time shelf life testing failed at 24 months

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2017· Microbiologics Inc

Recalled Item: Helix Elite" Molecular Standards: Inactivated Standard. Inactivated...

The Issue: Real-time shelf life testing failed at 24 months

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2017· Microbiologics Inc

Recalled Item: Microbiologics QC Sets and Panels: Helix Elite. Extended Enteric Bacterial...

The Issue: Real-time shelf life testing failed at 24 months

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2017· Microbiologics Inc

Recalled Item: Microbiologics QC Sets and Panels. BD MAX" CT/GC/TV Verification and...

The Issue: Real-time shelf life testing failed at 24 months

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2017· Angiodynamics, Inc.

Recalled Item: Accu2i pMTA Applicator Recalled by Angiodynamics, Inc. Due to The firm is...

The Issue: The firm is recalling product that has the potential to not function during...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2017· Zimmer Biomet, Inc.

Recalled Item: ECHO POR FMRL NC 9X125 Recalled by Zimmer Biomet, Inc. Due to Possibility...

The Issue: Possibility that the patient label inside the product box was incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2017· Zimmer Biomet, Inc.

Recalled Item: Lateral Troch Plate Full Crimp - 254mm Recalled by Zimmer Biomet, Inc. Due...

The Issue: Possibility that the patient label inside the product box was incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2017· Zimmer Biomet, Inc.

Recalled Item: CER BIOLOXD OPTION HD 32MM Recalled by Zimmer Biomet, Inc. Due to...

The Issue: Possibility that the patient label inside the product box was incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2017· Zimmer Biomet, Inc.

Recalled Item: COMP PRIMARY STEM 8MM MINI Recalled by Zimmer Biomet, Inc. Due to...

The Issue: Possibility that the patient label inside the product box was incorrectly...

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

Class II — Potential Health HazardOngoing