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.

1451–1475 of 76561

HighFDA (Food)·H-1047-2026·2026-06-10
Albertsons ahi poke products do not declare tuna allergen
Albertsons store-made ahi poke products, sold under three UPCs, are being recalled because the contains statement does not declare tuna. 23 units in total are affected.
Product
UPC 23952700000 POKE AHI LIMU UPC 23506700000 POKE AHI LIMU PREVIOUSLY FROZEN - CO UPC 23958200000 POKE AHI SALT & PEPPER This is Albertson's store-made item and sold by random weight at point of sale with grocery store's scal
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2308-2026·2026-06-10
Stapes prosthesis pistons carry an incorrect functional length on labeling
Titanium/fluoroplastic piston stapes prostheses are being recalled because the device labeling states an incorrect functional length. Seven units are affected.
Product
TITANIUM/FLUOROPLASTIC PISTON 0.6MM DIA X 3.75MM L Model/Catalog Number: 409-375 Product Description: Stapes Prosthesis
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2296-2026·2026-06-10
Avanta administration tube sets may not engage the flow control valve
Avanta Multi-Patient Administration Tube Sets are being recalled because supplier changes created a fit issue, so the stopcock cannot be reliably engaged with the Contrast Flow Control Valve.
Product
Avanta Multi-Patient Administration Tube Sets (AVA 500 MPAT (Part 2 of 2)) used with the Medrad¿ Avanta Injection System; Catalog number: AVA 500 MPAT (Part 2 of 2); Affected material numbers: 87629007, 60729458, 86566648;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0557-2026·2026-06-10
Kirkland Signature ultra strength antacid tablets contain metallic particles
Kirkland Signature Ultra Strength Antacid, calcium carbonate 1000 mg, made by Guardian Drug Company for Costco, is being recalled over small metallic particles in the tablets.
Product
KIRKLAND ULTRA STREGTH ANTACID 171AB — KIRKLAND ULTRA STREGTH ANTACID 171AB (CALCIUM CARBONATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0578-2026·2026-06-10
TopCare extra strength antacid tablets contain small metallic particles
TopCare Health Extra Strength Antacid Tablets, calcium carbonate 750 mg, are being recalled because of the presence of small metallic particles in the chewable tablets.
Product
TOPCARE EXTRA STRENGTH ANTACID — TOPCARE EXTRA STRENGTH ANTACID (CALCIUM CARBONATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2286-2026·2026-06-10
Philips Azurion 5M12 systems may show unusable dark fluoroscopy images
Philips Azurion 5M12 systems with the Roadmap Pro software key are being recalled because a pedal tap may produce a dark image that is not clinically usable.
Product
Philips Azurion 5M12, Model Numbers: 722227 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key
Category
Medical Device
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-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 (Devices)·Z-2290-2026·2026-06-10
Philips Azurion 7M12 Roadmap Pro may produce unusable dark images
Philips Azurion 7M12 systems with the Roadmap Pro software key are being recalled because a pedal tap may cause a dark, clinically unusable image on the next fluoroscopy run.
Product
Philips Azurion 7M12, Model Numbers: 722078, 722223 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0969-2026·2026-06-10
Albertsons cowboy cookies 18 count do not declare pecan allergen
Albertsons store-made Cookies Cowboy 18 count is being recalled because the contains statement does not declare pecan. 982 units are affected.
Product
UPC 22730900000 COOKIES COWBOY 18CT 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 (Food)·H-1012-2026·2026-06-10
Albertsons duo seafood salad with crackers does not declare whiting
Albertsons store-made Ready Meals Duo Seafood Salad with Crackers is being recalled because the contains statement does not declare whiting. 286 units are affected.
Product
UPC 27183100000 Ready Meals DUO SEAFOOD SALAD W/CRACKERS 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 (Drugs)·D-0575-2026·2026-06-10
GoodSense ultra strength antacid tablets contain small metallic particles
GoodSense Ultra Strength Antacid Tablets, calcium carbonate 1000 mg, are being recalled because of the presence of small metallic particles in the chewable tablets.
Product
GOODSENSE ULTRA STRENGTH ANTACID ASSORTED FRUIT — GOODSENSE ULTRA STRENGTH ANTACID ASSORTED FRUIT (CALCIUM CARBONATE)
Category
Drug
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 (Drugs)·D-0564-2026·2026-06-10
Market Basket ultra strength antacid tablets contain small metallic particles
Market Basket Antacid, calcium carbonate 1000 mg ultra strength, is being recalled because of the presence of small metallic particles in the chewable tablets.
Product
MARKET BASKET ANTACID Calcium Carbonate 1000 mg, ULTRA STRENGTH, 72 Tablets, Distributed by: De Moules Supermarkets, Inc.,Tewksbury, Mass 01875, UPC 0 49705 83149 6.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0571-2026·2026-06-10
Hy-Vee extra strength antacid tablets contain small metallic particles
Hy-Vee Extra Strength Antacid, calcium carbonate 750 mg, is being recalled because of the presence of small metallic particles in the chewable tablets.
Product
HyVee, Extra Strength Antacid, Calcium Carbonate 750 mg, 96 CHEWABLE TABLETS, DISTRIBUTED BY: HY-VEE INC., Inc., WEST DES MOINES, IA 50266, UPC: 0 75450 82497 1.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0565-2026·2026-06-10
CareOne extra strength calcium antacid tablets contain metallic particles
CareOne Extra Strength Calcium Antacid, calcium carbonate 750 mg, is being recalled because of the presence of small metallic particles in the chewable tablets.
Product
EXTRA STRENGTH ANTACID — EXTRA STRENGTH ANTACID (CALCIUM CARBONATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·H-0993-2026·2026-06-10
Albertsons cocktail tray does not declare almond allergen
An Albertsons store-made cocktail tray is being recalled because the contains statement does not declare almond.
Product
UPC 29133000000 TRAY COCKTAIL 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 (Food)·H-1026-2026·2026-06-10
Albertsons Cheeses of France platter does not declare almond
Albertsons store-made Platter Cheeses of France is being recalled because the contains statement does not declare almond. 31 units are affected.
Product
UPC 27837800000 PLATTER CHEESES OF FRANCE 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 (Food)·H-0985-2026·2026-06-10
Albertsons pistachio muffins do not declare walnut allergen
Albertsons store-made Pistachio Muffins in 2 count and 4 count packs are being recalled because the contains statement does not declare walnut. 354 units are affected.
Product
UPC 22321200000 MUFFINS PISTACHIO 2CT UPC 22770600000 MUFFINS PISTACHIO 4CT 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 (Food)·H-0962-2026·2026-06-10
Chocolate lady madeleine strawberry cakes do not declare almond allergen
Albertsons store-made Cake Pav Chocolate Lady Madeleines Strawberry is being recalled because the contains statement does not declare almond. Six units are affected.
Product
UPC 25491700000 Cake Pav Chocolate Lady Madeleines Strawberry. 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 (Food)·H-0958-2026·2026-06-10
Albertsons colossal Dubai cheesecake slice does not declare pistachio
Albertsons store-made Cheesecake Slice Colossal Dubai is being recalled because the contains statement does not declare pistachio. 32 units are affected.
Product
UPC 25216200000 Cheesecake Slice Colossal Dubai. 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-2297-2026·2026-06-10
BD Pyxis MedStation 4000 fingerprint scanner may overheat and burn
The BD Pyxis MedStation 4000 medication cabinet is being recalled because the fingerprint scanner may overheat to a temperature capable of causing a first degree burn.
Product
BD Pyxis MedStation 4000 REF: 303 Medication cabinet
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-1044-2026·2026-06-10
Albertsons ready meals meatloaf does not declare anchovy allergen
Albertsons store-made Ready Meals Meatloaf is being recalled because the contains statement does not declare anchovy. 353 units are affected.
Product
UPC 21409600000 READY MEALS MEATLOAF SS COLD 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-2289-2026·2026-06-10
Philips Azurion 7B20/15 systems may show unusable dark fluoroscopy images
Philips Azurion 7B20/15 systems with the Roadmap Pro software key are being recalled because a pedal tap may produce a dark image that is not clinically usable. 156 units affected.
Product
Philips Azurion 7B20/15, Model Numbers: 722068, 722226 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0968-2026·2026-06-10
Albertsons gourmet Dubai cookies do not declare pistachio
Albertsons store-made Gourmet Dubai Cookie is being recalled because the contains statement does not declare pistachio.
Product
UPC 25185700000 COOKIE GOURMET DUBAI 1CT 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