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. 2,579 recalls have been distributed to New Mexico in the last 12 months.

48,595 total recalls
2,579 in last 12 months

Showing 57815800 of 48,595 recalls

DrugApril 19, 2024· Nomax Inc

Recalled Item: FUL-GLO Recalled by Nomax Inc Due to Failed Impurities/Degradation...

The Issue: Failed Impurities/Degradation Specifications: The Active Pharmaceutical...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 19, 2024· Philips North America Llc

Recalled Item: Patient Information Center iX and Patient Information Center iX Expand...

The Issue: Event Catalog information does not save when copied and transferred from one...

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

Class II — Potential Health HazardOngoing
FoodApril 18, 2024· Graceleigh, Inc. dba Sammy's Milk

Recalled Item: Sammy's Milk GOAT MILK TODDLER FORMULA Recalled by Graceleigh, Inc. dba...

The Issue: FDA inspection and investigation of firm's website and social media pages...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 18, 2024· Graceleigh, Inc. dba Sammy's Milk

Recalled Item: Sammy's Milk GOAT MILK TODDLER FORMULA Recalled by Graceleigh, Inc. dba...

The Issue: FDA inspection and investigation of firm's website and social media pages...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 18, 2024· Stryker Neurovascular

Recalled Item: The Synchro2 Guidewires are a steerable guidewire family with a Recalled by...

The Issue: Stryker Neurovascular has observed an increased frequency of PTFE coating...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2024· BD SWITZERLAND SARL

Recalled Item: Alaris Pump Infusion Set Low Sorbing Tubing (PE Lined) Back Recalled by BD...

The Issue: Due to infusion set tubing drip chamber becoming detached from the tubing...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2024· Stryker Neurovascular

Recalled Item: The Synchro SELECT Guidewires are a steerable guidewire family with Recalled...

The Issue: Stryker Neurovascular has observed an increased frequency of PTFE coating...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2024· Stryker Neurovascular

Recalled Item: The Synchro Neuro Guidewires are a steerable guidewire family with Recalled...

The Issue: Stryker Neurovascular has observed an increased frequency of PTFE coating...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2024· Olympus Corporation of the Americas

Recalled Item: OES 4000 Hysteroscope Recalled by Olympus Corporation of the Americas Due to...

The Issue: The required leakage test was not performed following of a re-work for a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2024· Boston Scientific Neuromodulation Corporation

Recalled Item: Vercise Genus Deep Brain Stimulation (DBS) Implantable Pulse Generator IPG:...

The Issue: Deep Brain Stimulation (DBS) Implantable Pulse Generator (IPG) may...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2024· OptumHealth Care Solutions LLC

Recalled Item: Optum Nimbus II Plus Recalled by OptumHealth Care Solutions LLC Due to...

The Issue: Nimbus II Plus, Infusion Pump Systems, manufactured by InfuTronix, are being...

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

Class I — Serious Health HazardOngoing
DrugApril 17, 2024· ARG Laboratories, Inc.

Recalled Item: Pain Wizard Recalled by ARG Laboratories, Inc. Due to Out of Specification...

The Issue: Out of Specification for active ingredient. Violative grade of propylene...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 17, 2024· ARG Laboratories, Inc.

Recalled Item: Pain Wizard Recalled by ARG Laboratories, Inc. Due to Out of Specification...

The Issue: Out of Specification for active ingredient. Violative grade of propylene...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 17, 2024· ARG Laboratories, Inc.

Recalled Item: NATURAL PAIN RELIEVING CREAM Recalled by ARG Laboratories, Inc. Due to Out...

The Issue: Out of Specification for active ingredient. Violative grade of propylene...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 17, 2024· ARG Laboratories, Inc.

Recalled Item: NATURAL PAIN RELIEVING CREAM Recalled by ARG Laboratories, Inc. Due to Out...

The Issue: Out of Specification for active ingredient. Violative grade of propylene...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 17, 2024· ARG Laboratories, Inc.

Recalled Item: NATURAL PAIN RELIEVING CREAM Recalled by ARG Laboratories, Inc. Due to Out...

The Issue: Out of Specification for active ingredient. Violative grade of propylene...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 17, 2024· ARG Laboratories, Inc.

Recalled Item: NATURAL PAIN RELIEVING CREAM Recalled by ARG Laboratories, Inc. Due to Out...

The Issue: Out of Specification for active ingredient. Violative grade of propylene...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 17, 2024· ARG Laboratories, Inc.

Recalled Item: Pain Wizard Recalled by ARG Laboratories, Inc. Due to Out of Specification...

The Issue: Out of Specification for active ingredient. Violative grade of propylene...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 17, 2024· ARG Laboratories, Inc.

Recalled Item: ALOE GATOR Recalled by ARG Laboratories, Inc. Due to Out of Specification...

The Issue: Out of Specification for active ingredient

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 17, 2024· ARG Laboratories, Inc.

Recalled Item: ALOE GATOR Recalled by ARG Laboratories, Inc. Due to Out of Specification...

The Issue: Out of Specification for active ingredient

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

Class II — Potential Health HazardOngoing
Refund