All recall categories

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.

1,959 stored notices name New Mexico, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach New Mexico too — those are in the archive.

Medical devices

Reported Apr 30, 2025

Radiometer ABL90 Series - Radiometer ABL90 FLEX Model Number 393-090 Radiometer ABL90 Series - Radiometer ABL90 FLEX…

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

Radiometer Medical ApS

FDA (openFDA device enforcement)

Medical devices

Reported Apr 30, 2025

Tempus Pro Patient Monitor, REFs: 00-1004-R (Tempus Pro non-printer, IBP, without headset dock), 00-1007-R and 00-1007…

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

Remote Diagnostic Technologies Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 23, 2025

Brand Name: Ballard Product Name: Closed Suction Catheters Model/Catalog Number: 198 Software Version: N/A Product…

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

Avanos Medical, Inc.

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 23, 2025

BD 4 Fr Single-Lumen PowerPICC Catheters, REF: 3174155, CK000540, 3174118, CK000483, 3174335, 3174355, CK000196,…

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

Bard Access Systems, Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 23, 2025

Trader Joe's Hot Honey Mustard Dressing (SKU #80152), packaged in glass bottle with tamper overwrap on plastic cap, net…

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

Reser's Fine Foods, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 23, 2025

t:slim X2 Insulin Pump with Interoperable Technology

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

Tandem Diabetes Care, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 23, 2025

HeartMate Mobile Power Unit: REF: 107754, NA; 107758, EU; 107758AU, AU; 107758UK, UK; L107758, EU Rental. Used with…

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

Thoratec LLC

FDA (openFDA device enforcement)

Medical devices

Reported Apr 23, 2025

Brand Name: AutoPulse NXT Resuscitation System Product Name: AutoPulse NXT Platform Model/Catalog Number: Model 200…

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

ZOLL Circulation, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 16, 2025

BD Pyxis" MedBank" Mini and BD Pyxis" MedBank" Tower, BD Pyxis" MedFlex, BD Pyxis" MedBank" MedPass are automated…

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

CareFusion 303, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 9, 2025

BD Connecta BD Luer-Lok 360, REF 394910 UDI-DI code: 00382903949106 Connecta¿ Plus 1 and Connecta¿ Plus 3 2-way and…

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

Bd Switzerland Sarl

FDA (openFDA device enforcement)

Medical devices

Reported Apr 9, 2025

DxC 500 AU Clinical Chemistry Analyzer, Catalog Numbers/UDI codes: C63519 / 14987666545058 C63520 / 14987666545065 The…

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

Beckman Coulter Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 2, 2025

CVAC Aspiration System, REF: CVC127020-1, and User Manual L00018. Intended for endoscopic examination/treatment of…

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

Calyxo, Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 2, 2025

Flor de Michoacan Blue Hawaiian Artificially Flavored Beverage Concentrate. 1 Gallon (3.78L) Pasteurized. Keep Frozen.…

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

Paletas Ice Cream, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Apr 2, 2025

CardioMEMS Heart Failure (HF) System that consist of: -CardioMEMS Hospital System Model CM3100 -CardioMEMS Backend Web…

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

St. Jude Medical

FDA (openFDA device enforcement)

Medical devices

Reported Mar 26, 2025

Introcan Safety 3 Closed IV Catheter 22 Ga. x 1 in., PUR, Winged. Passive safety IV catheter.

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

B Braun Medical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 26, 2025

BD Pyxis: Anesthesia Station ES, REF: 327, MedStation ES, REF: 323, MedStation ES Tower, REF: 352, CII Safe ES, REF:…

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

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 26, 2025

Microstream Instructions for Use and Part Number used with - Product Description, REF: FilterLine H Set & VitaLine H…

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

Oridion Medical 1987 Ltd.

9 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 19, 2025

CINNABON CLASSIC CINNAMON ROLL INTERNATIONAL delight COFFEE CREAMER 32 FL OZ (1 QT) 946 mL UPC 0 41271 01993 3…

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

Danone Wave

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 19, 2025

Brand Name: Da Vinci 5 Product Name: ASSY,DV5 CONSOLE,IS5000 Foot Tray Pedals Model/Catalog Number: 380730 Software…

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

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 19, 2025

Green Chile Bean Burrito, 15 days refrigerated at 33 45 degrees Fahrenheit. 120 days frozen at or below 32 degrees…

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

Mi Ranchito Foods, Incorporated

FDA (openFDA food enforcement)

Food

Reported Mar 19, 2025

Ulker Kekstra Mini strawberry, item 3792, 5.3oz foil pack, 10 per case, UPC 8690766082307

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

ZB Importing LLC

5 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 12, 2025

Rotarex Atherectomy System and Instructions for Use, BD SET Rotarex: S 6 F x 110 cm, REF: 80236; S 6 F x 135 cm, REF:…

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

Bard Peripheral Vascular Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 12, 2025

Brand Name: TBS Osteo Product Name: TBS iNsight Model/Catalog Number: TBS iNsight v3.x / pn: OS-TBSi Software Version:…

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

Medimaps Group

FDA (openFDA device enforcement)

Medical devices

Reported Mar 12, 2025

Paradigm REF: MMT-712 and MMT-715

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

Medtronic MiniMed, Inc.

11 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.