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. 1,925 recalls have been distributed to New Mexico in the last 12 months.
Showing 15721–15740 of 27,850 recalls
Recalled Item: Immunoglobulin M is an in vitro diagnostic assay for the Recalled by Abbott...
The Issue: An update to the Reagents and Specimen Collection and Handling/Preparation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAREstream ProNox Nitrous Oxide Delivery System labeled as the following:...
The Issue: Two analgesic gas delivery system oxygen/nitrous oxide mixers were reported...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MegaPower Electrosurgical Generator Recalled by Megadyne Medical Products,...
The Issue: If two devices are plugged into the same channel/port in the generator, both...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Draeger Jaundice Meter JM-103 The device is intended for use in hospitals...
The Issue: Users have misinterpreted the display for out of range measurement indicated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Draeger Jaundice Meter JM-105 The device is intended for use in hospitals...
The Issue: Users have misinterpreted the display for out of range measurement indicated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AdvanDx QuickFISH Slides Recalled by Opgen Inc Due to Possible diminished...
The Issue: Possible diminished performance prior to its established expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Minicon Clinical Sample Concentrators for In Vitro Diagnostic Use 9031...
The Issue: In vitro diagnostic devices, used greater than 6 months after date of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safety Sideport Knife 1.0mm 45¿ Recalled by Beaver Visitec Due to Blades are...
The Issue: Blades are loose in handles and may fall out due to non cured epoxy
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard Knee System PS Tibial Bearing Recalled by Zimmer Biomet, Inc. Due...
The Issue: The label master file was errantly set up as a 63/37mm instead of a 63/67mm....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus JF-160F duodenoscopes (Model NumberJF-160F) Recalled by Olympus...
The Issue: Issuance of validated, new reprocessing procedures. The new cleaning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus JF-140F duodenoscopes (Model NumberJF-140F) Recalled by Olympus...
The Issue: Issuance of validated, new reprocessing procedures. This corrective action...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RS 5F DL XPP KIT Recalled by Angiodynamics Inc. (Navilyst Medical Inc.) Due...
The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bio-Stable 5F SL-55CM IR-145 Kit Valved with Nitinol GW PG Recalled by...
The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XCELA PASV 5F SL 55CM IR-145 Nitinol Wire KIT PG Recalled by Angiodynamics...
The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: microTargeting" STar" Drive System (Motorized) Recalled by FHC, Inc. Due to...
The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: microTargeting" STar" Drive System (Motorized) Recalled by FHC, Inc. Due to...
The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: microTargeting" Drive System Distributed by Medtronic Recalled by FHC, Inc....
The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: microTargeting" Drive System Recalled by FHC, Inc. Due to The FHC Depth Stop...
The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: microTargeting" Lead Adapter for STar" Drive Recalled by FHC, Inc. Due to...
The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: microTargeting" STar" Drive System (Manual) Distributed by Medtronic...
The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.