Product Recalls in New Mexico
Product recalls affecting New Mexico — including food, drugs, consumer products, medical devices, and vehicles distributed to New Mexico. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 980 recalls have been distributed to New Mexico in the last 12 months.
Showing 28301–28320 of 48,595 recalls
Recalled Item: Ingenuity Core 128 (Model No. 728323) 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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Recalled Item: EliquisTablets 5mg Recalled by Bristol-myers Squibb Company Due to Labeling:...
The Issue: Labeling: Label Mix-up: One bottle of Eliquis 5 mg tablet was found to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Progesterone Injection in Olive Oil With Benzyl Alcohol 10% Recalled by...
The Issue: Lack of Processing Controls: The metal container closure adheres to the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: RED SEXP DSTL FEM 19CM LT ASSY 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.
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.
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.
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.
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.