State

New Mexico product recalls

72,936 recalls have nationwide distribution and so reach New Mexico. 3,625 additional recalls listed New Mexico specifically in their distribution scope.

What the numbers show

Total: 3,625
Critical: 747
Severe: 647
Most recent: 2026-09-02

Of the 3,625 recalls naming New Mexico we have scored against our rubric, 747 (21%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 647 (18%) are Severe.

Which agencies issued them

These figures cover only the 3,625 recalls whose distribution notice names New Mexico specifically. The 72,936 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1426–1450 of 76561

SevereFDA (Devices)·Z-2255-2026·2026-06-10
BD Whitacre spinal trays across nine catalog numbers recalled over bupivacaine
BD Spinal Trays with Whitacre needle 25 G, spanning nine catalog numbers, are being recalled as a sub-recall of the Huons bupivacaine product recall. 13,320 units affected.
Product
BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 400866, 405672, 405673, 405674, 405675, 405709, 405721, 405723, 406704.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2249-2026·2026-06-10
BD Quincke 25G spinal trays recalled in Huons bupivacaine sub-recall
BD Spinal Trays with Quincke needle 25 G, which contain bupivacaine with dextrose, are being recalled as a sub-recall of the Huons bupivacaine product recall. 3,130 units are affected.
Product
BD¿Spinal Tray with BD¿Quincke Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 405621, 405735.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2253-2026·2026-06-10
BD combined Whitacre and Quincke spinal trays recalled over bupivacaine
BD Spinal Trays containing both a Whitacre 25 G and a Quincke 22 G needle are being recalled as a sub-recall of the Huons bupivacaine product recall. 290 units affected.
Product
BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in., BD¿Quincke Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405741.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2251-2026·2026-06-10
BD Whitacre 22G spinal trays recalled in Huons bupivacaine sub-recall
BD Spinal Trays with Whitacre needle 22 G, which contain bupivacaine with dextrose, are being recalled as a sub-recall of the Huons bupivacaine product recall. 330 units are affected.
Product
BD¿Spinal Tray with BD¿Whitacre Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405645.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-0910-2026·2026-06-10
Cold prep cream sauce contains dry milk recalled for Salmonella
Cold Prep Cream Sauce in 20 lb bags is being recalled because it contains a dry milk powder ingredient recalled by the supplier over potential Salmonella contamination.
Product
Cold Prep Cream Sauce, 20 lb., packaged in a tied poly bag and packed 1 bag per case, UPC 0039954922458
Category
Food
Distribution
41 states
SevereFDA (Devices)·Z-2257-2026·2026-06-10
BD Whitacre 25G spinal trays recalled in Huons bupivacaine sub-recall
BD Spinal Trays with Whitacre needle 25 G, catalog numbers 405637 and 405707, are being recalled as a sub-recall of the Huons bupivacaine product recall. 5,940 units are affected.
Product
BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 405637, 405707.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2223-2026·2026-06-10
Ivenix pump software may report false battery health and shut down
The Ivenix Infusion System Large Volume Pump software is being recalled because a software anomaly can report a false battery-health value and trigger a shutdown alarm.
Product
LVP software of the Ivenix Infusion System (IIS); Product Code LVP-SW-0005.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-0909-2026·2026-06-10
Alfredo sauce contains dry milk powder recalled over Salmonella
Alfredo Sauce in 3 lb 7 oz sealed poly bags is being recalled because it contains a dry milk powder ingredient recalled by the supplier over potential Salmonella contamination.
Product
Alfredo Sauce, 3 lb. 7 oz., packaged in a sealed poly bag and packed 12 bags per case, UPC 0039954921963
Category
Food
Distribution
41 states
SevereFDA (Devices)·Z-2252-2026·2026-06-10
BD Whitacre 24 gauge spinal trays recalled over bupivacaine quality issues
BD Spinal Trays with a Whitacre 24 G needle, catalog numbers 400868 and 405652, are being recalled as a sub-recall of the Huons bupivacaine product recall. 3,550 units affected.
Product
BD¿Spinal Tray with BD¿Whitacre Needle 24 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 400868, 405652.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-0907-2026·2026-06-10
Cheese sauce mixes contain dry milk powder recalled over Salmonella
Cheese Sauce Mix and Creamier Cheese Sauce Mix are being recalled because they contain a dry milk powder ingredient recalled by the supplier over potential Salmonella contamination.
Product
1) Cheese Sauce Mix, 25.5 oz., packaged in a sealed poly bag and packed 12 bags per case, UPC 0399549125016 2) Cheese Sauce Mix, 25 lb., packaged in a tied poly bag and packed 1 bag per case, UPC 0039954924308 3) Creamier Cheese Sauce Mix, 25 lb., packaged in a tied poly bag an
Category
Food
Distribution
41 states
SevereFDA (Devices)·Z-2277-2026·2026-06-10
Spinocan spinal needle kits recalled over Huons bupivacaine quality issues
Spinocan spinal needle procedure kits are being recalled because they contain Bupivacaine Hydrochloride in Dextrose Injection subject to the Huons recall. 16,080 units affected.
Product
Spinocan Spinal Needle procedure kits: Material Description (Material Number): Spinocan 26 Ga. x 3-1/2 in. (90 mm), Bupivacaine 0.75% with Dextrose 8.25% Tray (Kit) (333201); Spinocan 25 Ga. x 3-1/2 in. (90 mm), Bupivacaine 0.75% with Dextrose 8.25% Tray (Kit) (333211); Spin
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2256-2026·2026-06-10
BD spinal trays recalled as a sub-recall of Huons bupivacaine
BD Spinal Trays with Whitacre needle, which contain bupivacaine with dextrose, are being recalled as a sub-recall of the Huons bupivacaine product recall.
Product
BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405671.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-0908-2026·2026-06-10
Aramark cheese sauce contains dry milk powder recalled over Salmonella
Aramark Cheese Sauce New & Improved in 25 lb bags is being recalled because it contains a dry milk powder ingredient recalled by the supplier over potential Salmonella contamination.
Product
Aramark Cheese Sauce New & Improved, 25 lb., packaged in a tied poly bag and packed 2 bags per case, UPC 0039954925121
Category
Food
Distribution
41 states
HighFDA (Drugs)·D-0566-2026·2026-06-10
CareOne ultra strength antacid tablets contain small metallic particles
CareOne Ultra Strength Calcium Antacid, calcium carbonate 1000 mg, is being recalled because of the presence of small metallic particles in the chewable tablets.
Product
ULTRA STRENGTH ANTACID ASSORTED BERRIES — ULTRA STRENGTH ANTACID ASSORTED BERRIES (CALCIUM CARBONATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0569-2026·2026-06-10
Family Wellness ultra strength antacid tablets contain metallic particles
A further lot of Family Wellness Ultra Strength Antacid Tablets, calcium carbonate 1000 mg, is being recalled because of small metallic particles in the chewable tablets.
Product
FAMILY WELLNESS, ULTRA STRENGT, ANTACID TABLETS, Calcium Carbonate 1000 mg, 72 CHEWABLE TABLETS, DISTRIBUTED BY: MIDWOOD BRANDS, LLC, 500 VOLVO PKWY, CHESAPEAKE, VA 23320 USA., UP: 0 32251-92282-4.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·H-1025-2026·2026-06-10
Pad Thai chicken with pot stickers does not declare anchovy
Albertsons store-made Ready Meals Wok Pad Thai Chicken with Pot Stickers is being recalled because the contains statement does not declare anchovy. 39 units are affected.
Product
UPC 21380100000 Ready Meals WOK PAD THAI CHICKEN WITH POT STICKERS SS This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2294-2026·2026-06-10
Digital angiography and radiography systems may remain energized when switched off
Digital angiography and radiography systems are being recalled because contactors in the high voltage generator may weld together, leaving the power supply energized when the system is off.
Product
Digital Angiography System Trinias:UD150G-40 / D150GC-40; Digital Angiography System BRANSIST safire:UD150G-40 / D150GC-40; Digital Angiography System BRANSIST alexa:UD150G-40 / D150GC-40; Digital Radiography System RADspeed Pro: UD150B-40 / UD150V-40 / UD150L-40 / UD150L-40E/D15
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2279-2026·2026-06-10
CASE cardiac testing systems may spark at the printer head
CASE v7.0 Cardiac Testing Systems are being recalled because electrical sparking may occur at the printer head, and ignition of thermal paper could cause serious thermal injury.
Product
CASE v7.0 Cardiac Testing System Model no. 3031234-001 Product Code SU3
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0562-2026·2026-06-10
Casey's extra strength antacid tablets contain small metallic particles
Casey's Extra Strength Antacid, calcium carbonate 750 mg chewable tablets, is being recalled because of the presence of small metallic particles in the tablets.
Product
Extra strength Antacid Calcium Carbonate 750 mg, chewable tablets, 96-count bottle, DISTRIBUTED BY CASEY'S MARKETING COMPANY, ANKENY, IA 50521, UPC: 0 98437 24361 9.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0574-2026·2026-06-10
GoodSense antacid chewable tablets contain small metallic particles
GoodSense Extra Strength Antacid Tablets, calcium carbonate 750 mg, are being recalled because of the presence of a foreign substance: small metallic particles in the chewable tablets.
Product
GOODSENSE EXTRA STRENGTH ANTACID — GOODSENSE EXTRA STRENGTH ANTACID (CALCIUM CARBONATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0556-2026·2026-06-10
Ascend amlodipine and olmesartan tablets failed dissolution specifications
Amlodipine and Olmesartan Medoxomil Tablets, 5 mg/40 mg, are being recalled after failing dissolution specifications, with olmesartan medoxomil content below specification.
Product
AMLODIPINE AND OLMESARTAN MEDOXOMIL — AMLODIPINE AND OLMESARTAN MEDOXOMIL (AMLODIPINE AND OLMESARTAN MEDOXOMIL)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0572-2026·2026-06-10
Hy-Vee ultra strength antacid tablets contain small metallic particles
Hy-Vee Ultra Strength Antacid, calcium carbonate 1000 mg, is being recalled because of the presence of small metallic particles in the chewable tablets.
Product
HyVee, Ultra Strength Antacid, Calcium Carbonate 1000 mg, 72 CHEWABLE TABLETS, DISTRIBUTED BY: HY-VEE INC., Inc., WEST DES MOINES, IA 50266, UPC: 0 75450 82514 5.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0558-2026·2026-06-10
Tums assorted fruit antacid tablets contain small metallic particles
Tums Antacid Assorted Fruit tablets, calcium carbonate 1000 mg in 160-count bottles, are being recalled because of small metallic particles in the chewable tablets.
Product
HALEON CALCIUM CARBONATE TUMS ANTACID, Assorted Fruit Tablets, 1000 mg, 160-count bottle, Haleon, Warren, NJ 07059, UPC 3 07660 74610 2.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0576-2026·2026-06-10
Equaline extra strength antacid tablets contain small metallic particles
Equaline Extra Strength Antacid Tablets, calcium carbonate 750 mg, are being recalled because of the presence of small metallic particles in the chewable tablets.
Product
EQUALINE EXTRA STRENGTH ASSORTED BERRY ANTACID — EQUALINE EXTRA STRENGTH ASSORTED BERRY ANTACID (CALCIUM CARBONATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·H-0988-2026·2026-06-10
Albertsons 16-inch carving tray does not declare walnut
An Albertsons store-made 16-inch carving tray is being recalled because the contains statement does not declare walnut. 12 units are affected.
Product
UPC 29168800000 CARVING TRAY 16IN FS This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide