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. 1,046 recalls have been distributed to New Mexico in the last 12 months.
Showing 14701–14720 of 48,595 recalls
Recalled Item: f'real Made to Order Shake Base - 8 fl oz Recalled by Rich Products Corp Due...
The Issue: Shake base contains undeclare milk due to wrong outer-label stating product...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ALPHA MALE+ Male Enhancer Recalled by Alpha-Tek LLC Due to Marketed Without...
The Issue: Marketed Without an Approved NDA/ANDA: FDA analysis determined the presence...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: RUSCH Endotracheal Tube oral/nasal Magill Recalled by Teleflex Medical...
The Issue: The firm received reports that the endotracheal tube cuff could be inflated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH Slick Set Cuffed Endotracheal Tube and Stylet Set Recalled by Teleflex...
The Issue: The firm received reports that the endotracheal tube cuff could be inflated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH Flexi-Set Cuffed Endotracheal Tube and Stylet Set Recalled by Teleflex...
The Issue: The firm received reports that the endotracheal tube cuff could be inflated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Recalled by Philips North America LLC Due to Infant/Child...
The Issue: Infant/Child defibrillator pads contain incorrect labeling. This could lead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH Endotracheal Tube oral/nasal Murphy Eye Recalled by Teleflex Medical...
The Issue: The firm received reports that the endotracheal tube cuff could be inflated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cell Marque Antibodies Recalled by Cell Marque Corporation Due to Mouse...
The Issue: Mouse Monoclonal Antibody labelled with an incorrect expiry date of 31 Dec...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Normand Remisol Advance Data Manager Recalled by Beckman Coulter Inc. Due to...
The Issue: There is a potential that the data management system may add additional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Ingenia Ambition X (Product Number 781356) Recalled by Philips North...
The Issue: The sealed magnet will experience uncontrolled shutdown known as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Colonoscope Family # 1-Pentax Video Colonoscopes (EC Family) with One...
The Issue: Updated Reprocessing Instruction For Use (rIFU): Impacted PENTAX Medical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smith&nephew BHR SQUARE HEADED NAIL Recalled by Smith & Nephew Orthopaedics...
The Issue: The nail head may become detached during surgery.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLASH Ostial System Recalled by Ostial Corporation Due to Angioplasty system...
The Issue: Angioplasty system has a manufacturing issue that has the potential to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gastroscope Family # 1-Gastroscopes without a Water Jet Channel Models:...
The Issue: Updated Reprocessing Instruction For Use (rIFU): Impacted PENTAX Medical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neutrogena Ultra Sheer body mist sunscreen BROAD SPECTRUM SPF 70 Recalled by...
The Issue: cGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Neutrogena Ultra Sheer body mist sunscreen BROAD SPECTRUM SPF 45 Recalled by...
The Issue: cGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Neutrogena Beach Defense water+sun protection sunscreen spray BROAD SPECTRUM...
The Issue: cGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Neutrogena COOLDRY SPORT sunscreen spray BROAD SPECTRUM SPF 100 Recalled by...
The Issue: cGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Neutrogena Ultra Sheer body mist sunscreen BROAD SPECTRUM SPF 100+ Recalled...
The Issue: cGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Neutrogena Ultra Sheer body mist sunscreen BROAD SPECTRUM SPF 30 Recalled by...
The Issue: cGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.