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. 2,567 recalls have been distributed to New Mexico in the last 12 months.
Showing 7741–7760 of 27,850 recalls
Recalled Item: (1) GE Centricity Universal Viewer 6.0 Recalled by GE Healthcare, LLC Due to...
The Issue: Inaccurate Distance and Area measurements with use of Global Stack viewport.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips EPIQ Ultrasound Systems (various models) used in conjunction with...
The Issue: Retroactive: Ultrasound may experience an unexpected automatic reboot,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Exacta-Mix 2400 compounding system Recalled by Baxter Healthcare...
The Issue: There is a potential for leaking valves on ports 1 to 4 in certain lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARIES SARS-CoV-2 Assay Recalled by Luminex Corporation Due to SARS-CoV-2...
The Issue: SARS-CoV-2 assay that detects SARS-CoV-2 ORF1ab and N genes may not detect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas e801 Immunoassay Analyzer Recalled by Roche Diagnostics Operations,...
The Issue: Software issue resulting in signals and sample test results of Pre-Wash...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Grappler Suture Anchor Recalled by Paragon 28, Inc. Due to Suture anchor may...
The Issue: Suture anchor may break upon insertion, which could lead to potential debris...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProPlan CMF Anatomical Model Recalled by Materialise USA LLC Due to...
The Issue: MU22-INA-DUQ case was labeled as MU22-INA-DUQ but was shipped with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surpria 64: Software Version V3.11 Recalled by FUJIFILM Healthcare Americas...
The Issue: Error 00003050 or 00003052 may occur during scanning, the captured images...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SCENARIA View: Software Version V1.08 Recalled by FUJIFILM Healthcare...
The Issue: Error 00003050 or 00003052 may occur during scanning, the captured images...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surpria: Software Version V3.11 Recalled by FUJIFILM Healthcare Americas...
The Issue: Error 00003050 or 00003052 may occur during scanning, the captured images...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Sensis or Sensis Vibe Combo systems as follows: System Recalled by...
The Issue: The Sensis Signal Input Box provides hooks as a milled item on the bottom of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HXBL/WETEX/Genesis Biomedical Viral Transport Container Recalled by Haimen...
The Issue: Distributed VTM outside of VTM Guidance and without clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HXBL/WETEX/Genesis Biomedical Viral Transport Container Recalled by Haimen...
The Issue: Distributed VTM outside of VTM Guidance and without clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HXBL/WETEX/Genesis Biomedical Viral Transport Container Recalled by Haimen...
The Issue: Distributed VTM outside of VTM Guidance and without clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SafeControl handset (a component of the Sentida bed which moves Recalled by...
The Issue: When the handset is disconnected from the power mains, and mains operation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pentacam AXL Recalled by Oculus Optikgeraete GMBH Due to Due to a software...
The Issue: Due to a software issue, IOL calculator printout often does not accurately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pentacam AXL Wave . Used to image the anterior segment of the eye. Recalled...
The Issue: Due to a software issue, IOL calculator printout often does not accurately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pentacam HR . Used to image the anterior segment of the eye. Recalled by...
The Issue: Due to a software issue, IOL calculator printout often does not accurately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ShockPulse-SE Lithotripsy Generator Model/Serial: SPL-S Recalled by Olympus...
The Issue: Mis-wired component-the improperly wired component can result in additional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZAP-X Radiosurgery System Recalled by Zap Surgical Systems Due to Software...
The Issue: Software issue identified in cases of initial patient setup with large...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.