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. 1,078 recalls have been distributed to New Mexico in the last 12 months.
Showing 9441–9460 of 27,850 recalls
Recalled Item: Arrow Pacing Catheter Kit-Bipolar Electrode Catheter 5 Fr. 110 cm Recalled...
The Issue: Marketed without a 510K
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Temporary Pacing Catheter/Introducer Kit 6Fr. pacing catheter 7Fr....
The Issue: Marketed without a 510K
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Bipolar Balloon Electrode Catheter 5 Fr. 105 cm Recalled by Arrow...
The Issue: Marketed without a 510K
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Temporary Pacing Catheter/Introducer Kit 5Fr. pacing catheter 6 Fr....
The Issue: Marketed without a 510K
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5 Fr IR PowerPICC Convenience Kit Catheter Dual Lumen with Recalled by Bard...
The Issue: Catheter convenience kits contain the incorrect guidewire. Kits were labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GENOSYL DS Recalled by Vero Biotech, LLC Due to Reports received of NO...
The Issue: Reports received of NO measured below desired dose during transition between...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEGION Posterior Stabilized OXINIUM Femoral Component Recalled by Smith &...
The Issue: The device components experienced a manufacturing process error that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost C90 High Performance. radiography and fluoroscopy system...
The Issue: Following a system restart where the Table Height 2 (TH2) is the default...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost 4 Flex / Value. radiography and fluoroscopy system Recalled...
The Issue: Following a system restart where the Table Height 2 (TH2) is the default...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost C90 Flex/Value/Chest/ER. radiography and fluoroscopy system...
The Issue: Following a system restart where the Table Height 2 (TH2) is the default...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProxiDiagnost N90. radiography and fluoroscopy system Recalled by Philips...
The Issue: Following a system restart where the Table Height 2 (TH2) is the default...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost 4 High Performance. radiography and fluoroscopy system...
The Issue: Following a system restart where the Table Height 2 (TH2) is the default...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cortoss Bone Augmentation Material 5cc Cartridge Recalled by Stryker Spine...
The Issue: The products experienced a 12-hour excursion from the required temperature...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cortoss Bone Augmentation Material 10cc Cartridge Recalled by Stryker Spine...
The Issue: The products experienced a 12-hour excursion from the required temperature...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ADVIA Chemistry XPT Chemistry System Recalled by Siemens Healthcare...
The Issue: ADVIA Chemistry System and Software Versions (V1.4 SMN 11314625 and V1.4...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JELCO HYPODERMIC NEEDLE-PRO FIXED NEEDLE INSULIN SYRINGE: a) 1.0mL 28G...
The Issue: Specific models and lot numbers of the Jelco Hypodermic Needle-Pro Fixed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal Pacemaker Tray Pgybk Recalled by DeRoyal Industries Inc Due to...
The Issue: DeRoyal manufactured certain lots of surgical procedure pack products using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal Angio Cath Removal Tray Recalled by DeRoyal Industries Inc Due to...
The Issue: DeRoyal manufactured certain lots of surgical procedure pack products using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ExacTrac Dynamic software Recalled by Brainlab AG Due to Display of...
The Issue: Display of potential patient movement might be delayed to the user for high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic LINQ II Model Number # LNQ22 Insertable Cardiac Monitor Recalled...
The Issue: Device fail to detect Brady episodes, Pause (Asystole) episodes and PVC's...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.