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.

48,595 total recalls
1,078 in last 12 months

Showing 6981–7000 of 27,850 recalls

Medical DeviceDecember 8, 2022· Medtronic Navigation, Inc.

Recalled Item: RadiaLux Lighted Retractor (Pink) Recalled by Medtronic Navigation, Inc. Due...

The Issue: Defect in sterile pouch seal, incomplete seal, of lighted Retractors,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: CENTURION MEDICAL PRODUCTS...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: a) CENTURION MEDICAL PRODUCTS CHEST...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: MEDLINE LCPH LAB DRAW KIT Recalled by...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: a) MEDLINE GENERAL UTILITY Recalled by...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: a) CENTURION MEDICAL PRODUCTS CENTRAL...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· The Anspach Effort, Inc.

Recalled Item: 6.5 cm Pediatric Craniotome Attachment. Use with XMax¿ Recalled by The...

The Issue: Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: MEDLINE PAIN TRAY Recalled by MEDLINE...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· Mobius Imaging, LLC

Recalled Item: MobiCT-32 AIRO Mobile CT Scanner Recalled by Mobius Imaging, LLC Due to...

The Issue: Stryker received one report of an injury to an untrained user that occurred...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: MEDLINE CABG PACK Recalled by MEDLINE...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: CENTURION MEDICAL PRODUCTS NEONATAL...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: MEDLINE PREP TRAY Recalled by MEDLINE...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: MEDLINE PERF. ASSOC. CUT DOWN TRAY...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: MEDLINE BREAST BIOPSY KIT Recalled by...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Surgical convenience kits labeled as: MEDLINE ARM/MINOR DRAPE CSTM Recalled...

The Issue: The recall is due to the perforated bag not allowing for outside of the kit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· Philips Respironics, Inc.

Recalled Item: Philips Garbin Ventilator Recalled by Philips Respironics, Inc. Due to The...

The Issue: The replacement silicone sound abatement foam installed into some Trilogy...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 7, 2022· The Anspach Effort, Inc.

Recalled Item: Adult Craniotome Intended for cutting and shaping bone Recalled by The...

The Issue: Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE 2000 Thyroglobulin (OUS). For in vitro diagnostic use with Recalled...

The Issue: Potential for Functional Sensitivity to not meet Instructions For Use (IFU)...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· The Anspach Effort, Inc.

Recalled Item: 7.5 cm Large Craniotome Attachment Use with XMax¿ Recalled by The Anspach...

The Issue: Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· The Anspach Effort, Inc.

Recalled Item: 7.5 cm Large Rotating Craniotome Attachment. Use with XMax¿ Recalled by The...

The Issue: Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing