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Recalls distributed in New Mexico

These notices name New Mexico in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.

1,993 stored notices name New Mexico, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,743 notices were distributed nationwide, so they reach New Mexico too — those are in the archive.

Medical devices

Reported Oct 22, 2025

FERNO POWER X2 POWERED AMBULANCE COT, Model/Catalog Number: 0015816; FOR USE IN GROUND TRANSPORTATION AMBULANCES.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ferno-Washington Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 22, 2025

Airvo 2, REF: PT101US, and myAirvo 2, REF: PT100US, used with Disinfection Kit User Manual, REF: UI-185043723

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Fisher & Paykel Healthcare, Ltd.

FDA (openFDA device enforcement)

Food

Reported Oct 22, 2025

Fruit Cocktail IN 100% JUICE WITH ADDED INGREDIENTS; NET WT 15 OZ (425 g); Ingredients: Diced Peaches, Diced Pears,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Pacific Coast Producers

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Oct 22, 2025

Brand Name: Branding is not applied to this product. Product Name: DVI display cables Model/Catalog Number: 012-0895-01…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Spacelabs Healthcare, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 22, 2025

6+ Months SPROUT ORGANICS Made With Organic Sweet Potato, Apple & Spinach NET WT. 3.5 OZ (99g) INGREDIENTS: ORGANIC…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Sprout Organics Inc.

FDA (openFDA food enforcement)

Food

Reported Oct 22, 2025

Dole Apple Juice (primary package), 15.2 Fl oz., PET, 12 bottles per case, Refrigerate after opening

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Tropicana Brands Group

FDA (openFDA food enforcement)

Medical devices

Reported Oct 15, 2025

PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. x 3-1/2 in. (9cm) Tuohy Epidural Needle - Winged and…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

B Braun Medical Inc.

12 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 15, 2025

Kirkland Signature brand Ahi Tuna Wasabi Poke, Costco #17193, net wt. 1lb. Product is packaged in clear plastic…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Western United Fish Company Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Oct 8, 2025

Venclose digiRF Generators, Model VCRFG1, with software 3.35 designed to identify internal wiring anomalies in the…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Bard Peripheral Vascular Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 8, 2025

Brand Name: Atlan Product Name: Atlan A350 Model/Catalog Number: 8211500 Software Version: Not applicable Product…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Draeger, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 8, 2025

Getinge 88-Series Washer- Disinfector. Model Number: 88-5.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Getinge Disinfection Ab

FDA (openFDA device enforcement)

Medical devices

Reported Oct 8, 2025

NES Reprocessed 0.9mm OTW Turbo Elite Laser Atherectomy Catheter. Model Number: R-410-152. The NES Reprocessed…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Northeast Scientific Inc.

7 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 8, 2025

Lipton Green Tea Citrus. 16.9 ounce PET Bottle. sold as 12pk. Outer case label reads as , "*** Lipton Green Tea Citrus…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Pepsico Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Oct 8, 2025

IMPLANT EPIKUT PLUS MT16 3,5X10,0MM, REF: ILM 3510N; IMPLANT EPIKUT PLUS MT16 3.8X11.5MM, REF: ILM 3511N; IMPLANT…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

S.I.N. Implant System Ltda

FDA (openFDA device enforcement)

Medical devices

Reported Oct 8, 2025

GORE ACUSEAL Vascular Graft, REF: ECH050020J, ECH050020W, ECH050050J, ECH050050W, ECH060010A, ECH060020A, ECH060020J,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

W L Gore & Associates, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 1, 2025

STRATAFIX Spiral PDS Plus Bidirectional Knotless Tissue Control Device, SFX SPI PDS+ BI VIO 14X14IN(36X36CM) USP1(M4)…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ethicon, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Sep 24, 2025

Vercise Deep Brain Stimulation Systems Surgical Implant Manual, Document Number: 92328632-09

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Boston Scientific Neuromodulation Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Sep 24, 2025

SureStep Foley Tray System Bardex I.C. Complete Care Infection Control Foley Catheter Tray, REF: A303316A

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

C.R. Bard Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 24, 2025

FORMUTECH NUTRITION FLEXIBLE JOINT FORMULA WITH CISSUS QUADRANGULARIS SUPPORTS TENDONS & MUSSCLES PROMOTES HEALTH…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Hi-Tech Pharmaceuticals Inc.

15 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Sep 24, 2025

CHARGE-UP CHILAQUILES Traditional Mexican breakfast consisting of tortilla chips smothered in a spicy tomatillo salsa…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Itacate Foods LLC

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Sep 24, 2025

Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial Ref: MX2-3DC use in conjunction with the SmartDrive MX2+…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Max Mobility LLC

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 24, 2025

Pinnacle Radiation Therapy Planning System: Multimodality Simulation Workspace 18.0.5 Model 870258 UDI code:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips Medical Systems (Cleveland) Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 10, 2025

Superion IDS Kit Superion Indirect Decompression System 8MM, VF Implant 101-9808 00884662000529 Superion Indirect…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Boston Scientific Neuromodulation Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Sep 10, 2025

Brand Name: MediHoney ¿ Product Name: MediHoney¿ Paste Model/Catalog Number: 31505 Product Description: MediHoney¿…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Integra LifeSciences Corp. (NeuroSciences)

7 more products in this recall

FDA (openFDA device enforcement)

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RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.