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. 1,699 recalls have been distributed to New Mexico in the last 12 months.

48,595 total recalls
1,699 in last 12 months

Showing 4642146440 of 48,595 recalls

Medical DeviceOctober 26, 2012· Hospira Inc.

Recalled Item: Plum A+ Hyperbaric Single Channel Infusion Pumps with Hospira MedNet...

The Issue: The volume control knob on some Plum A+ single channel infusers (located on...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2012· Volk Optical Inc

Recalled Item: 20 Diopter Binocular Indirect Ophthalmoscope (BIO) Lens For visualization...

The Issue: The defect was with mis-engraving of the lot # directly on the product and...

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

Class III — Low RiskOngoing
Medical DeviceOctober 25, 2012· Carl Zeiss Meditec, Inc.

Recalled Item: INTRABEAM Balloon Applicator Set Recalled by Carl Zeiss Meditec, Inc. Due to...

The Issue: A manufacturing defect has been identified which could results in the small...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2012· Stryker Howmedica Osteonics Corp.

Recalled Item: Hoffman LRF Wire Bolt Recalled by Stryker Howmedica Osteonics Corp. Due to...

The Issue: Two complaints have been filed where Hoffman LRF Wires have broken during...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2012· Carl Zeiss Meditec, Inc.

Recalled Item: INTRABEAM Balloon Applicator Set Recalled by Carl Zeiss Meditec, Inc. Due to...

The Issue: A manufacturing defect has been identified which could results in the small...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2012· Verathon, Inc.

Recalled Item: The GlideScope Video Laryngoscope (GVL) is a video laryngoscope that...

The Issue: Re-usable video laryngoscope blades of the GlideScope GVL3, GVL4, and GVL5...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 25, 2012· Philips Healthcare Inc.

Recalled Item: Philips DigitalDiagnost X-Ray System with Eleva Software 2.1.3 Model numbers...

The Issue: When the operator for a wall stand view selects an "image rotation"...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2012· Quasar Bio-Tech, Inc. dba Silver Bay LLC

Recalled Item: Quasar Power Pack contains a Baby Quasar and a Baby Recalled by Quasar...

The Issue: Quasar Bio-Tech is recalling their Baby Quasar, Baby Quasar Pink, Quasar...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2012· Kerr Corporation

Recalled Item: BioPlant Recalled by Kerr Corporation Due to The firm initiated the recall...

The Issue: The firm initiated the recall becaue disturbing the BioPlant product soon...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2012· Quasar Bio-Tech, Inc. dba Silver Bay LLC

Recalled Item: Baby Quasar (LAB-001-D Recalled by Quasar Bio-Tech, Inc. dba Silver Bay LLC...

The Issue: Quasar Bio-Tech is recalling their Baby Quasar, Baby Quasar Pink, Quasar...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2012· Quasar Bio-Tech, Inc. dba Silver Bay LLC

Recalled Item: Quasar MD is an infrared LED lamp that is labeled Recalled by Quasar...

The Issue: Quasar Bio-Tech is recalling their Baby Quasar, Baby Quasar Pink, Quasar...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2012· Carl Zeiss Meditec, Inc.

Recalled Item: INTRABEAM Balloon Applicator Set Recalled by Carl Zeiss Meditec, Inc. Due to...

The Issue: A manufacturing defect has been identified which could results in the small...

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

Class II — Potential Health HazardOngoing
DrugOctober 25, 2012· Hospira Inc.

Recalled Item: Epinephrine Injection USP Recalled by Hospira Inc. Due to Presence of...

The Issue: Presence of Particulates; may contain glass particles

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 25, 2012· Red Chamber Company

Recalled Item: Frozen Yellowfin Tuna Loin 3/5 Recalled by Red Chamber Company Due to Red...

The Issue: Red Chamber is recalling Frozen Yellowfin Tuna Loin due to customer...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 24, 2012· BumbleBar, Inc.

Recalled Item: Gluten Free Cafe Cinnamon Sesame Bar. The Retail Carton has Recalled by...

The Issue: Gluten Free Cafe Cinnamon Sesame Bar is recalled due to the potential to be...

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 24, 2012· BumbleBar, Inc.

Recalled Item: Gluten Free Cafe Chocolate Sesame Bar. The Retail Carton has Recalled by...

The Issue: Gluten Free Cafe Chocolate Sesame Bar is recalled due to the potential to be...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 24, 2012· Superstat Corp

Recalled Item: Superstat Modified Collagen Hemostatic Sponge Recalled by Superstat Corp Due...

The Issue: The recall was initiated because Superstat Corporation has confirmed that no...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2012· Superstat Corp

Recalled Item: Superstat Modified Collagen Hemostatic Sponge Recalled by Superstat Corp Due...

The Issue: The recall was initiated because Superstat Corporation has confirmed that no...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2012· Superstat Corp

Recalled Item: Superstat Modified Collagen Hemostatic Sponge Recalled by Superstat Corp Due...

The Issue: The recall was initiated because Superstat Corporation has confirmed that no...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2012· Superstat Corp

Recalled Item: Superstat Modified Collagen Hemostatic Sponge Recalled by Superstat Corp Due...

The Issue: The recall was initiated because Superstat Corporation has confirmed that no...

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

Class II — Potential Health HazardOngoing