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. 1,849 recalls have been distributed to New Mexico in the last 12 months.
Showing 24581–24600 of 27,850 recalls
Recalled Item: Ziehm Solo C-Arm Interventional Fluoroscopic X-Ray System. Mobile...
The Issue: Engineering change in 2006 resulted in a minor non-conformity of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ziehm Vista/Vista Plus C-Arm Interventional Fluoroscopic X-Ray System....
The Issue: Engineering change in 2006 resulted in a minor non-conformity of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ziehm Vision(2) FD C-Arm Interventional Fluoroscopic X-Ray System. Mobile...
The Issue: Engineering change in 2006 resulted in a minor non-conformity of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ziehm Vision R C-Arm Interventional Fluoroscopic X-Ray System. Mobile...
The Issue: Engineering change in 2006 resulted in a minor non-conformity of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Antimicrobial Susceptibility Testing Disc Recalled by Remel Inc Due to...
The Issue: Individual discs in the lot may not be sufficiently impregnated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWISTER PLUS 26mm Rotatable Retrieval Device (Box of 5 configuration)...
The Issue: Sterility of device may be compromised due to lack of pouch seal integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWISTER PLUS 26mm Rotatable Retrieval Device (Box of 10 configuration)...
The Issue: Sterility of device may be compromised due to lack of pouch seal integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWISTER PLUS 22mm Rotatable Retrieval Device (Box of 5 configuration)...
The Issue: Sterility of device may be compromised due to lack of pouch seal integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Indus Invue Screws: lM71059-XX: Indus Screw 04.2mm SelfDrilling. Used to...
The Issue: Mismarked and unmarked screws
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Indus Invue Screws: IM71013-XX: Indus Screw04.0mm SelfDrilling. Used to...
The Issue: Mismarked and unmarked screws
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWISTER PLUS 22mm Rotatable Retrieval Device (Box of 10 configuration)...
The Issue: Sterility of device may be compromised due to lack of pouch seal integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORCHESTRA/ORCHESTRA PLUS Programmer Recalled by Sorin Group Italia S.r.l....
The Issue: Sorin has voluntarily issued a notification to physicians related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Indus Invue Screws: IM71058-XX: 04.2mm Recalled by SpineFrontier, Inc. Due...
The Issue: Mismarked and unmarked screws
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pro clear(R) 1 day Sphere (o mafilcon A) Recalled by CooperVision Inc. Due...
The Issue: Lots were labeled with incorrect expiration dates on secondary package...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has recently become aware of a potential safety issue due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ClearSight(TM) Toric 1 day (ocufilcon D) Recalled by CooperVision Inc. Due...
The Issue: Lots were labeled with incorrect expiration dates on secondary package...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Indus Invue Screws: IM71016-XX: 04.5mm Recalled by SpineFrontier, Inc. Due...
The Issue: Mismarked and unmarked screws
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWISTER PLUS 26mm Rotatable Retrieval Device (Box of 1 configuration)...
The Issue: Sterility of device may be compromised due to lack of pouch seal integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWISTER PLUS 22mm Rotatable Retrieval Device (Box of 1 configuration)...
The Issue: Sterility of device may be compromised due to lack of pouch seal integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Asante Comfort Infusion Set with 110cm tubing & 13mm cannula packaged in...
The Issue: Reports of the infusion tubing disconnecting from the connector, resulting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.