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. 913 recalls have been distributed to New Mexico in the last 12 months.
Showing 44961–44980 of 48,595 recalls
Recalled Item: 8mm Precise Bipolar Forceps used in conjunction with the da Recalled by...
The Issue: Reports of dislodging of the Cautery Plug Insert from the Cautery Plug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GlideScope Video Laryngoscope (GVL) 3 Recalled by Verathon, Inc. Due to...
The Issue: Verathon GlideScope Reusable GVL and AVL Blades are being recalled due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Air Dermatome II Recalled by Zimmer Surgical Inc Due to This removal...
The Issue: This removal is in response to complaints alleging that the Zimmer Air...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Zimmer Air Dermatome Recalled by Zimmer Surgical Inc Due to This removal...
The Issue: This removal is in response to complaints alleging that the Zimmer Air...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Air Dermatome II Recalled by Zimmer Surgical Inc Due to This removal...
The Issue: This removal is in response to complaints alleging that the Zimmer Air...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InSpan Inserter Recalled by SpineFrontier, Inc. Due to Potential for set...
The Issue: Potential for set screw to be come deformed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Benefiber Plus Heart Health Non-Thickening Powder Recalled by Novartis...
The Issue: The products are being recalled due to the receipt of a relatively high...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Benefiber Fiber Supplement Plus Calcium Recalled by Novartis Consumer Health...
The Issue: The products are being recalled due to the receipt of a relatively high...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Benefiber Fiber Drink Mix Recalled by Novartis Consumer Health Due to The...
The Issue: The products are being recalled due to the receipt of a relatively high...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Benefiber Fiber Drink Mix Recalled by Novartis Consumer Health Due to The...
The Issue: The products are being recalled due to the receipt of a relatively high...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Benefiber Non-Thickening Powder Recalled by Novartis Consumer Health Due to...
The Issue: The products are being recalled due to the receipt of a relatively high...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Benefiber Fiber Supplement Recalled by Novartis Consumer Health Due to The...
The Issue: The products are being recalled due to the receipt of a relatively high...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Derma-Smoothe/FS (fluocinolone acetonide) Topical Oil (SCALP OIL) Recalled...
The Issue: Subpotent Drug: the active ingredient, fluocinolone acetonide, was found to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lightning ROD capsules Recalled by Chang Kwung Products Due to Undeclared...
The Issue: Marketed Without An Approved NDA/ANDA: Lightning Rod capsules are being...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lightning ROD capsules Recalled by Chang Kwung Products Due to Undeclared...
The Issue: Marketed Without An Approved NDA/ANDA: Lightning Rod capsules are being...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VITROS 5600 Integrated System (product code 6802413) Product Usage: For...
The Issue: There is evidence that an electrical short within the systems connector has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Versaport Bladeless Optical Trocar With Fixation Cannula - 5mm Product...
The Issue: Seals may disengage from the cannula which may result in a component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to There is evidence...
The Issue: There is evidence that an electrical short within the systems connector has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Versaport Bladeless Optical Trocar With Fixation Cannula - 5mm Short...
The Issue: Seals may disengage from the cannula which may result in a component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 3600 Immunodiagnostic System (product code 6802783) Product Usage:...
The Issue: There is evidence that an electrical short within the systems connector has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.