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. 969 recalls have been distributed to New Mexico in the last 12 months.

48,595 total recalls
969 in last 12 months

Showing 30881–30900 of 48,595 recalls

FoodOctober 11, 2016· Roland Foods, LLC.

Recalled Item: Roland¿ Preserved Lemons Recalled by Roland Foods, LLC. Due to Undeclared...

The Issue: The product contains undeclared sulfites based on sampling and analysis by...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodOctober 10, 2016· Rosa Foods HQ

Recalled Item: Soylent Food Bars Recalled by Rosa Foods HQ Due to Rosa Foods is recalling...

The Issue: Rosa Foods is recalling Soylent Bar because a number of their customers have...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 10, 2016· St Jude Medical Inc.

Recalled Item: Quadra Assura Recalled by St Jude Medical Inc. Due to St Jude Medical is...

The Issue: St Jude Medical is recalling implantable cardiac defibrillator (ICD) and...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 10, 2016· St Jude Medical Inc.

Recalled Item: Unify Recalled by St Jude Medical Inc. Due to St Jude Medical is recalling...

The Issue: St Jude Medical is recalling implantable cardiac defibrillator (ICD) and...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 10, 2016· St Jude Medical Inc.

Recalled Item: Fortify VR Recalled by St Jude Medical Inc. Due to St Jude Medical is...

The Issue: St Jude Medical is recalling implantable cardiac defibrillator (ICD) and...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 7, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Advia Chemistry Calibrator For in vitro diagnostic use in the Recalled by...

The Issue: Siemens has confirmed that the DBIL_2 Assigned Calibrator Values (ACV)...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: Bearing Sleeve Recalled by The Anspach Effort, Inc. Due to Supplied...

The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: Rotating Adult Craniotome Product Usage: Pneumatic system Recalled by The...

The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: Foot Control without Switches Recalled by The Anspach Effort, Inc. Due to...

The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: Reciprocating MICRO SAW Recalled by The Anspach Effort, Inc. Due to Supplied...

The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: Keyless Driver Product Usage: Pneumatic system Recalled by The Anspach...

The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: 14cm QD Angle Attachment Product Usage: Pneumatic system Recalled by The...

The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: Electric Handpiece EM Hand Control Product Usage: Electric system Recalled...

The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: 6.8cm Controlled Depth Attachment Product Usage: Pneumatic system Recalled...

The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: SMALL ATTACHMENT Recalled by The Anspach Effort, Inc. Due to Supplied...

The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: IMRI AIR CONTROL Product Usage: Pneumatic system Recalled by The Anspach...

The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: 14cm QD Angle Attachment Product Usage: Product attachment Recalled by The...

The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: XMAX Motor Recalled by The Anspach Effort, Inc. Due to Supplied Directions...

The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: 12.6CM TAPERED ATTACHMENT Recalled by The Anspach Effort, Inc. Due to...

The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: Autolube-III Product Usage: Pneumatic system Recalled by The Anspach Effort,...

The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...

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

Class II — Potential Health HazardOngoing