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 7621–7640 of 27,850 recalls

Medical DeviceAugust 1, 2022· ICU Medical, Inc.

Recalled Item: 6" (15 cm) Appx 0.85 ml Recalled by ICU Medical, Inc. Due to Due to a...

The Issue: Due to a manufacturing defect which results in a visible gap between the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2022· MERCHSOURCE LLC

Recalled Item: The product is a handheld ultraviolet-C germicidal wand and contains two...

The Issue: Excessive ultraviolet-C radiation

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2022· ICU Medical, Inc.

Recalled Item: MicroClave Clear Neutral Connector Recalled by ICU Medical, Inc. Due to Due...

The Issue: Due to a manufacturing defect which results in a visible gap between the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2022· ICU Medical, Inc.

Recalled Item: 6.5" (17 cm) Appx 0.84 ml Recalled by ICU Medical, Inc. Due to Due to a...

The Issue: Due to a manufacturing defect which results in a visible gap between the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2022· CAREFUSION

Recalled Item: BD MaxGuard Extension Set with 1.2 Micron Filter and Needleless Y-Site...

The Issue: Administration set, and extension set product labels list expiration year...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2022· ICU Medical, Inc.

Recalled Item: 6.5 IN (17 cm) APPX 0.78 ml Recalled by ICU Medical, Inc. Due to Due to a...

The Issue: Due to a manufacturing defect which results in a visible gap between the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2022· CAREFUSION

Recalled Item: BD MaxGuard Extension Set Recalled by CAREFUSION Due to Administration set,...

The Issue: Administration set, and extension set product labels list expiration year...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2022· ICU Medical, Inc.

Recalled Item: MicroClave Clear Neutral Connector. A bidirectional connector used as an...

The Issue: Due to a manufacturing defect which results in a visible gap between the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2022· Hobbs Medical, Inc.

Recalled Item: Hobbs Medical Polypectomy Snare Catalog Number: 7202 Recalled by Hobbs...

The Issue: Device label display an incorrect expiration date, extends the shelf life of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2022· Hobbs Medical, Inc.

Recalled Item: Hobbs Scope Introducer Catalog Number: 4650 Recalled by Hobbs Medical, Inc....

The Issue: Device label display an incorrect expiration date, extends the shelf life of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2022· Hobbs Medical, Inc.

Recalled Item: Freeman Pancreatic Flexi-Stent Catalog Number: 6535 Recalled by Hobbs...

The Issue: Device label display an incorrect expiration date, extends the shelf life of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2022· Hobbs Medical, Inc.

Recalled Item: Hobbs Biliary Pigtail Stent Kits (containing 3412) Catalog Number:6004...

The Issue: Device label display an incorrect expiration date, extends the shelf life of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2022· Hobbs Medical, Inc.

Recalled Item: Freeman Pancreatic Flexi-Stent Kit Catalog Number: 6351 Recalled by Hobbs...

The Issue: Device label display an incorrect expiration date, extends the shelf life of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2022· Hobbs Medical, Inc.

Recalled Item: Freeman Pancreatic Flexi-Stent Kit Catalog Number: 6352 Recalled by Hobbs...

The Issue: Device label display an incorrect expiration date, extends the shelf life of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2022· Hobbs Medical, Inc.

Recalled Item: Freeman Pancreatic Flexi-Stent Kit (containing 6352) Catalog Number: 6321...

The Issue: Device label display an incorrect expiration date, extends the shelf life of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2022· Hobbs Medical, Inc.

Recalled Item: Hobbs Medical Grasping Forceps Catalog Number: 5008 Recalled by Hobbs...

The Issue: Device label display an incorrect expiration date, extends the shelf life of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2022· Hobbs Medical, Inc.

Recalled Item: Hobbs Medical Polypectomy Snare Catalog Number: 4564 Recalled by Hobbs...

The Issue: Device label display an incorrect expiration date, extends the shelf life of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2022· Hobbs Medical, Inc.

Recalled Item: Freeman Pancreatic Flexi-Stent Kit (containing 6566) Catalog Number: 6518...

The Issue: Device label display an incorrect expiration date, extends the shelf life of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2022· Hobbs Medical, Inc.

Recalled Item: Hobbs Medical Grasping Forceps Catalog Number:5004 Recalled by Hobbs...

The Issue: Device label display an incorrect expiration date, extends the shelf life of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2022· Hobbs Medical, Inc.

Recalled Item: Hobbs Retrieval Forceps Catalog Number: 5018 Recalled by Hobbs Medical, Inc....

The Issue: Device label display an incorrect expiration date, extends the shelf life of...

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

Class II — Potential Health HazardOngoing