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. 1,816 recalls have been distributed to New Mexico in the last 12 months.

48,595 total recalls
1,816 in last 12 months

Showing 2994129960 of 48,595 recalls

FoodFebruary 17, 2017· Diamond Crystal Brands Inc

Recalled Item: Natural Cocoa Powder 10-12% cocoa butter Recalled by Diamond Crystal Brands...

The Issue: During sanitation, the firm discovered metal pieces missing from a sifter...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 17, 2017· Diamond Crystal Brands Inc

Recalled Item: Natural Cocoa Powder 22-24% cocoa butter Recalled by Diamond Crystal Brands...

The Issue: During sanitation, the firm discovered metal pieces missing from a sifter...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 17, 2017· Diamond Crystal Brands Inc

Recalled Item: Baking Powder Net Wt. 5 lbs. (2.27 kg) packaged 6 bags per case Recalled by...

The Issue: During sanitation, the firm discovered metal pieces missing from a sifter...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 17, 2017· Zimmer Biomet, Inc.

Recalled Item: various polyethylene implants Sports Med Repicci II Tibial Components...

The Issue: Endotoxin levels higher than process maximum limits were discovered in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2017· Zimmer Biomet, Inc.

Recalled Item: various polyethylene implants Knees Revision Tibial Tray Systems Oxford...

The Issue: Endotoxin levels higher than process maximum limits were discovered in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2017· Zimmer Biomet, Inc.

Recalled Item: various polyethylene implants BIO PLUG 10MM Product Usage: Non-weight...

The Issue: Endotoxin levels higher than process maximum limits were discovered in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2017· Zimmer Biomet, Inc.

Recalled Item: various polyethylene implants Hips Active Articulation ArComXL Bearings...

The Issue: Endotoxin levels higher than process maximum limits were discovered in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2017· Zimmer Biomet, Inc.

Recalled Item: various polyethylene implants Extremities Recalled by Zimmer Biomet, Inc....

The Issue: Endotoxin levels higher than process maximum limits were discovered in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2017· Zimmer Biomet, Inc.

Recalled Item: various polyethylene implants Custom parts Product Usage: Custom Recalled by...

The Issue: Endotoxin levels higher than process maximum limits were discovered in the...

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

Class II — Potential Health HazardOngoing
DrugFebruary 16, 2017· Organic Herbal Supply

Recalled Item: XtraHRD Natural Male Enhancement Capsules Recalled by Organic Herbal Supply...

The Issue: Marketed without an Approved NDA/ANDA: Product contains N-desmethyl...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 16, 2017· Allegiant Health

Recalled Item: HealthA2Z CHEWABLE Aspirin (NSAID) 81 mg Recalled by Allegiant Health Due to...

The Issue: cGMP deviations - presence of rubber particles found loose in the bulk product.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 16, 2017· Merit Medical Systems, Inc.

Recalled Item: 7F Prelude¿ Short Sheath Introducer. Catalog Numbers: K15-00070 Recalled by...

The Issue: Merit Medical Systems, Inc. announces a voluntary field action for sheaths...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 16, 2017· Crossroads Extremity Systems Llc

Recalled Item: MotoCLIP(TM) Super Elastic Fusion System Recalled by Crossroads Extremity...

The Issue: Seven 18mm x 18mm x 18 mm implants had been placed in kits, packed and...

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

Class II — Potential Health HazardOngoing
DrugFebruary 15, 2017· Pharmedium Services Llc

Recalled Item: Ropivacaine HCl 0.2% 400 mL Total Volume in an ON-Q Recalled by Pharmedium...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugFebruary 15, 2017· Pharmedium Services Llc

Recalled Item: Ropivacaine HCl 0.2% 500 mL Total Volume in an ON-Q Recalled by Pharmedium...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugFebruary 15, 2017· Pharmedium Services Llc

Recalled Item: Ropivacaine HCl 0.2% 750 mL Total Volume in an ON-Q Recalled by Pharmedium...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugFebruary 15, 2017· Pharmedium Services Llc

Recalled Item: Ropivacaine HCl 0.2% 500 mL Total Volume in an ON-Q Recalled by Pharmedium...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugFebruary 15, 2017· Pharmedium Services Llc

Recalled Item: Bupivacaine HCl 0.25% 270 mL Total Volume in an ON-Q Recalled by Pharmedium...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugFebruary 15, 2017· Pharmedium Services Llc

Recalled Item: Bupivacaine HCl 0.25% 400 mL Total Volume in an ON-Q Recalled by Pharmedium...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugFebruary 15, 2017· Pharmedium Services Llc

Recalled Item: Ropivacaine HCl 0.2% 550 mL Total Volume in an AutoFuser Recalled by...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund