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. 2,585 recalls have been distributed to New Mexico in the last 12 months.
Showing 4961–4980 of 27,850 recalls
Recalled Item: Impella Connect Recalled by Abiomed, Inc. Due to The following features have...
The Issue: The following features have been disabled from the web-based portal because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vascu-Guard Peripheral Vascular Patch (GLOBAL) Recalled by Baxter Healthcare...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter FloSeal Hemostatic Matrix NL Recalled by Baxter Healthcare...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Flo-Rester Recalled by Baxter Healthcare Corporation Due to...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Coseal Premix Recalled by Baxter Healthcare Corporation Due to...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Peri-Guard Repair Patch Recalled by Baxter Healthcare Corporation Due to...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Flo-Thru Intraluminal Shunt Recalled by Baxter Healthcare Corporation...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERI-GUARD SUPPLE Recalled by Baxter Healthcare Corporation Due to...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Vascular Probe Recalled by Baxter Healthcare Corporation Due to...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter FloSeal Hemostatic Matrix RECOTHROM Recalled by Baxter Healthcare...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Neurovascular Recalled by Stryker, Inc. Due to The microcatheter IFU...
The Issue: The microcatheter IFU contains an intended use that has not been evaluated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Ostene Hemostasis Material Recalled by Baxter Healthcare Corporation...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Peri-Guard Repair Patch Recalled by Baxter Healthcare Corporation Due to...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Preveleak Surgical Sealant Recalled by Baxter Healthcare Corporation...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vascu-Guard Peripheral Vascular Patch (US) Recalled by Baxter Healthcare...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Neurovascular Recalled by Stryker, Inc. Due to The microcatheter IFU...
The Issue: The microcatheter IFU contains an intended use that has not been evaluated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ambu aView 2 A Monitor Recalled by Ambu Inc. Due to Instructions for Use...
The Issue: Instructions for Use have been updated to add the following warning: Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultrasound EA (Ergonomic Advantage) table versions Recalled by Oakworks Inc...
The Issue: Backrest platform stress fracture - the table is not operational in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultrasound EA (Ergonomic Advantage) table version Recalled by Oakworks Inc...
The Issue: Backrest platform stress fracture - the table is not operational in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultrasound EA (Ergonomic Advantage) table versions Recalled by Oakworks Inc...
The Issue: Backrest platform stress fracture - the table is not operational in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.