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. 1,709 recalls have been distributed to New Mexico in the last 12 months.

48,595 total recalls
1,709 in last 12 months

Showing 4186141880 of 48,595 recalls

Medical DeviceFebruary 20, 2014· Ortho-Clinical Diagnostics

Recalled Item: VITROS TT4 Calibrator For the quantitative measurement of total thyroxine...

The Issue: Total T4 Calibrators and Reagent Packs may have calibration failures or low...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2014· Biosense Webster, Inc.

Recalled Item: PENTARAY NAV High-Density Mapping Catheter and PENTARAY NAV ECO Catheter...

The Issue: Biosense Webster is recalling the PentaRay Nav Catheter because it has the...

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

Class II — Potential Health HazardOngoing
DrugFebruary 19, 2014· Gilead Sciences, Inc.

Recalled Item: Atripla (efavirenz 600 mg/ emtricitabine 200 mg/ tenofovir disoproxil...

The Issue: Presence of Foreign Substance: Red Silicone Rubber Particulates are Present...

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

Class III — Low RiskOngoing
Refund
Medical DeviceFebruary 19, 2014· Abbott Diabetes Care, Inc.

Recalled Item: FreeStyle Blood Glucose Monitors System. For in vitro diagnostic use...

The Issue: Abbott Diabetes Care has identified through internal testing and...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 19, 2014· Abbott Diabetes Care, Inc.

Recalled Item: FreeStyle Flash Blood Glucose Monitors System. Meter made in China Recalled...

The Issue: Abbott Diabetes Care has identified through internal testing and...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 19, 2014· Medefil Incorporated

Recalled Item: Heparin I.V. Flush Syringe is available is pre-filled polypropylene syringes...

The Issue: The bar code that is printed on the Master Carton label does not correspond...

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

Class III — Low RiskOngoing
FoodFebruary 18, 2014· Newman'S Own Inc.

Recalled Item: Newman's Own Salsa Con Queso Recalled by Newman'S Own Inc. Due to Undeclared...

The Issue: Undeclared wheat

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 18, 2014· Siemens Healthcare Diagnostics

Recalled Item: ADVIA Centaur XP Immunoassay system Recalled by Siemens Healthcare...

The Issue: Instrument Cover Gas Spring failures. Over time, the gas spring may lose its...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2014· Hospira Inc.

Recalled Item: GemStar Docking Station Recalled by Hospira Inc. Due to There are two...

The Issue: There are two situations that may occur when using the GemStar Docking...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 18, 2014· Remel Inc

Recalled Item: Oxoid Vancomycin 30 mcg Recalled by Remel Inc Due to Some of the discs may...

The Issue: Some of the discs may not be impregnated with the antibiotic.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2014· Philips Medical Systems, Inc.

Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Models: M3535A and M3536A with...

The Issue: When the HeartStart MRx.is used with the Q-CPR Meter in defibrillation mode,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2014· Philips Medical Systems, Inc.

Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Model numbers: M3535A Recalled...

The Issue: MRx may display a Red X in the Ready For Use (RFU) indicator during...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2014· Philips Medical Systems, Inc.

Recalled Item: HeartStart MRx Monitor/Defibrillator Recalled by Philips Medical Systems,...

The Issue: A component of the MRx Processor Board may be susceptible to damage from...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2014· Philips Medical Systems, Inc.

Recalled Item: HeartStart MRx Defibrillator/Monitor M3538A Lithium Ion Batteries Revision J...

The Issue: Philips HeartStart MRx Monitor/Defibrillator, when operating on battery...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2014· Philips Medical Systems, Inc.

Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Recalled by Philips Medical...

The Issue: ECG trunk cable and connector block of the MRx could be susceptible to...

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

Class II — Potential Health HazardOngoing
DrugFebruary 14, 2014· Medisca Inc

Recalled Item: CITRULLINE (L) in 25 g Recalled by Medisca Inc Due to Labeling: Label...

The Issue: Labeling: Label Mix-Up: FDA tested samples of API from Medisca, labeled as...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 14, 2014· Ben Venue Laboratories Inc

Recalled Item: Acetylcysteine Solution Recalled by Ben Venue Laboratories Inc Due to...

The Issue: Presence of Particulate Matter: During a review of retain samples, the firm...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 14, 2014· Legacy Pharmaceutical Packaging

Recalled Item: Fluoxetine Capsules Recalled by Legacy Pharmaceutical Packaging Due to...

The Issue: Chemical Contamination: The recalling firm received notice that their...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 14, 2014· Agila Specialties Private Ltd.

Recalled Item: etomidate injection Recalled by Agila Specialties Private Ltd. Due to...

The Issue: Presence of Particulate Matter: Potential for small black particles to be...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 14, 2014· Falafel King Ent, Inc.

Recalled Item: Falafel King Green Chile Hummus Recalled by Falafel King Ent, Inc. Due to...

The Issue: Falafel King is recalling their Green Chile Hummus because the green chile...

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

Class I — Serious Health HazardOngoing
Refund