State

New Mexico product recalls

73,738 recalls have nationwide distribution and so reach New Mexico. 3,636 additional recalls listed New Mexico specifically in their distribution scope.

What the numbers show

Total: 3,636
Critical: 745
Severe: 815
Most recent: 2026-10-28

Of the 3,636 recalls naming New Mexico we have scored against our rubric, 745 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 815 (22%) are Severe.

Which agencies issued them

These figures cover only the 3,636 recalls whose distribution notice names New Mexico specifically. The 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

31826–31850 of 77374

ModerateFDA (Food)·F-0559-2020·2020-01-15
Grey Ghost Bakery Lemon Sugar Cookies Recalled for Undeclared Sulfites
Grey Ghost Bakery is recalling Lemon Sugar cookies in various sizes due to undeclared sulfites. The product was distributed to numerous states across the US.
Product
GREY GHOST BAKERY scratch-made cookies LEMON SUGAR NET WT 1.4 OZ (40 G), UPC 8 53152 00308 1 , 4 OZ (113 G) UPC 8 53152 00332 6 & 8 OZ (225 G) UPC 8 53152 00307 4 GREY GHOST BAKERY 1750 SIGNAL POINT RD, STE 2A CHARLESTON, SC 29412
Category
Food
Distribution
41 states
ModerateFDA (Devices)·Z-0777-2020·2020-01-15
Nextremity Solutions Recalls Stratum MDS Screws Due to Length Discrepancy
Nextremity Solutions is recalling 86 Stratum MDS Screws because the components are 2mm shorter than indicated on the package label.
Product
Stratum MDS Screw 3.5x48mm ST Part Number: STRM-MDS-3548ST
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0783-2020·2020-01-15
Idelle Labs Recalls SURE 48 hr Anti-Perspirant for Labeling Error
Idelle Labs is recalling SURE 48 hr Confidence Unscented Anti-Perspirant & Deodorant because the label lists an active ingredient that is not actually in the product.
Product
SURE 48 hr Confidence Unscented invisible solid Anti-Perspirant & Deodorant, Net Wt. 2.6 oz (73g) NDC# 41595-5509-2 UPC 8 83484 71717 2 Made in Canada and Distributed by Idelle Labs, Ltd., El Paso, TX 79912
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0778-2020·2020-01-15
Nextremity Solutions Recalls Stratum MDS Screws Due to Length Discrepancy
Nextremity Solutions is recalling 86 Stratum MDS Screws because they are 2mm shorter than the length indicated on the package label.
Product
Stratum MDS Screw 3.5x50mm ST Part Number: STRM-MDS-3550ST
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0638-2020·2020-01-15
Lupin Recalls Blisovi Fe 1.5/30 Tablets Due to Crumbling
Lupin Pharmaceuticals is recalling Blisovi Fe 1.5/30 tablets because they crumble when removed from the blister pack.
Product
Blisovi Fe 1.5/30 (norethindrone acetate and ethinyl estradiol tablets USP and ferrous fumarate tablets 75mg), Rx Only, Distributed by: Lupin Pharmaceuticals Inc Baltimore, MD 21202, Manufactured for: Lupin Limited Pithampur 454775 INDIA 240875, NDC 68180-866-11
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0465-2020·2020-01-15
Wayfare Butterscotch Pudding Recalled for Package Bloating and Off Flavors
Wayfare Health Foods LLC is recalling Plant Based Butterscotch Pudding due to consumer complaints of package bloating, off flavors, and textural issues.
Product
Plant Based WayFare Butterscotch Pudding Organic Dairy Free, Item #1223. Net wt. 4 oz. There are 4/4 oz. cups per pack with cardboard overwrap. UPC 845681000372.
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0794-2020·2020-01-15
Baxter Recalls One-Link Needle-Free IV Connectors Due to Connection Force Issue
Baxter Healthcare is recalling One-Link Needle-Free IV Connectors because some units require higher-than-expected force to connect securely to standard Luer adapters.
Product
ONE-LINK Needle-free IV Connector, Product Codes: 7N8300, 7N8301, 7N8310, 7N8330K, 7N8332K, 7N8334K, 7N8370K, 7N8371, 7N8375K, 7N8376K, 7N8377, 7N8378, 7N8390, 7N8391, 7N8399 - Product Usage: intended for single patient use with a vascular access device for the administration of…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0786-2020·2020-01-15
Idelle Labs Recalls SURE 48hr Anti-Perspirant Due to Labeling Error
Idelle Labs is recalling SURE 48hr Confidence Unscented Anti-Perspirant because the label lists an active ingredient that is not actually in the product.
Product
SURE 48hr Confidence Unscented Original Solid Anti-Perspirant & Deodorant Net Wt 2.7 oz (76g) NDC# 41595-5513-2 UPC 8 83484 71794 3 Made in Canada and Distributed by Idelle Labs, Ltd., El Paso, TX 79912
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0784-2020·2020-01-15
Idelle Labs Recalls SURE Antiperspirant for Undeclared Active Ingredient
Idelle Labs is recalling SURE 48hr Confidence Nourishing Coconut Antiperspirant & Deodorant because the label lists an active ingredient that is not actually in the product.
Product
SURE 48hr Confidence Nourishing Coconut invisible solid Antiperspirant & Deodorant Net Wt 2.6 oz (73g) NDC# 41595-5547-1 UPC 8 83484 31020 5 Made in Canada and Distributed by Idelle Labs, Ltd., El Paso, TX 79912
Category
Drug
Distribution
Distributed nationwide
HighCPSC·20056·2020-01-14
Thompson's WaterSeal Aerosol Protectors Recalled for Fire Hazard
The Thompson's Company is recalling about 852,000 aerosol cans of WaterSeal wood and masonry protectors because leaking propellant poses a fire hazard.
Product
Thompson's® WaterSeal® Waterproofing Wood Protector and Masonry Protector in Aerosol Cans
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·20V012000·2020-01-13
Toyota and Lexus Recall Vehicles for Fuel Pump Failure Risk
Toyota is recalling approximately 1.8 million vehicles because a fuel pump failure could cause the engine to stall while driving, increasing crash risk.
Product
LEXUS — LEXUS, TOYOTA RC 350, CAMRY, ES350, RC 300
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V010000·2020-01-10
Genuine Scooter Recalls 2020 Royal Alloy GT150 Due to Brake Rotor Defect
Genuine Scooters is recalling 2020 Royal Alloy GT150 scooters because the front brake rotor may become uncentered, potentially causing a loss of braking and increasing crash risk.
Product
GENUINE SCOOTER — GENUINE SCOOTER ROYAL ALLOY
Category
Vehicle
Distribution
Distributed nationwide
SevereUSDA FSIS·002-2020·2020-01-10
Culinary International Recalls Chicken Burritos Due to Undeclared Egg Allergen
Culinary International is recalling approximately 626 pounds of frozen chicken burritos that actually contain eggs, an undeclared allergen. No illnesses have been reported.
Product
Ruiz Food Products, Inc. — Culinary International, LLC Recalls Chicken Burrito Products Due to Misbranding and Undeclared Allergens
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·20V011000·2020-01-10
GM Recalls 2007-2008 Trucks for Air Bag Inflator Defect
General Motors is recalling 2007-2008 Chevrolet Silverado and GMC Sierra trucks because front passenger air bag inflators may explode.
Product
CHEVROLET — CHEVROLET, GMC SILVERADO 2500, SIERRA 2500, SIERRA 3500, SILVERADO 3500
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V009000·2020-01-10
Forest River Recalls 2020 Shockwave Toyhauler Trailers for Incorrect Tire Placard
Forest River is recalling 2020 Shockwave Toyhauler SHT18FS-CA trailers because the Federal Placard lists incorrect tire pressure, which may increase crash risk.
Product
FOREST RIVER — FOREST RIVER SHOCKWAVE TOYHAULER
Category
Vehicle
Distribution
Distributed nationwide
CriticalNHTSA·20V007000·2020-01-09
Ferrari Recalls 458 Italia and California for Air Bag Defect
Ferrari is recalling 982 vehicles because front passenger air bag inflators may explode, posing a risk of serious injury or death.
Product
FERRARI — FERRARI 458 ITALIA, CALIFORNIA
Category
Vehicle
Distribution
Distributed nationwide
CriticalNHTSA·20V008000·2020-01-09
Nissan and Infiniti Recall Vehicles for Air Bag Inflator Defect
Nissan is recalling specific 2001-2011 Nissan and Infiniti vehicles because front passenger air bag inflators may explode due to propellant degradation.
Product
INFINITI — INFINITI, NISSAN M45, QX4, I30, I35
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·20050·2020-01-09
Holiday Travel Mugs Recalled Due to Fire Hazard in Microwaves
Boston Warehouse Trading Corp. is recalling Holiday Travel Mugs sold at Meijer because metallic print can spark in microwaves, posing a fire hazard.
Product
Holiday Travel Mugs
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·20712·2020-01-09
Little Bambino Tricycles Recalled for Lead Paint Violation and Poisoning Risk
Thesaurus Global Marketing is recalling Little Bambino tricycles because lead levels in the paint and components exceed federal bans, posing a poisoning risk to young children.
Product
Little Bambino 4 in 1 canopy children's tricycles
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·20051·2020-01-09
Libbey Glass Recalls 33.5 oz. Milk Bottles Due to Laceration Hazard
Libbey Glass is recalling 33.5 oz. milk bottles that can break unexpectedly during use, posing a laceration hazard. No injuries have been reported.
Product
33.5 oz. Milk Bottles
Category
Consumer Product
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0633-2020·2020-01-08
FDA Recalls Silver Bullet Male Enhancement Capsules for Undeclared Active Ingredient
The FDA is recalling Silver Bullet male enhancement capsules because they contain an undeclared active ingredient (Sildenafil) and were marketed without an approved NDA/ANDA.
Product
Silver Bullet, Get Bigger and Harder, Works in Minutes, Lasts for Days, 10 male enhancement capsules in blister foil package, 725mg per capsule, Distributed by Silver Bullet Ltd, Golden Springs, CO, USA, UPC: 610877392698.
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·20V006000·2020-01-08
KME Firestix Aerial Devices Recalled for Swing Drive Lubrication Defect
KME is recalling certain 2012-2015 and 2017 Firestix Aerial Devices because swing drives may lack lubricating oil, risking gear damage and uncontrolled ladder movement.
Product
KME — KME FIRESTIX
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0746-2020·2020-01-08
Thoratec HeartMate 3 Mobile Power Unit Recalled for Static Electricity Risk
Thoratec Corp. is recalling HeartMate 3 Mobile Power Units because excessive static electricity can cause unrecoverable power loss, potentially reducing blood flow from the left ventricular assist system.
Product
HeartMate 3 Mobile Power Unit, REF 107754, UDI or GTIN: 00813024010883, and 107758, UDI or GTIN: 00813024010890, when connected to the HeartMate 3 Left Ventricular Assist System, REF 106524US, UDI or GTIN: 00813024013297, and 106524, UDI or GTIN: 00813024011712 - Product Usage…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0631-2020·2020-01-08
American Health Packaging Recalls Ranitidine Syrup Due to NDMA Impurity
American Health Packaging is recalling specific lots of Ranitidine Syrup because the presence of the NDMA impurity was detected in the product.
Product
Ranitidine Syrup (Ranitidine Oral Solution USP), 15 mg/mL, 150 mg/10 mL per cup, Rx Only, Distributed by: American Health Packaging, Columbus, Ohio. (a) Case of 50 cups (NDC 60687-260-69) (b) Case of 40 cups (NDC 60687-260-23 (c) Unit Dose Cup (NDC 60687-260-69)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0765-2020·2020-01-08
Villa Sistemi Medicali Recalls Apollo DRF X-ray Tables Due to Chain Failure
Villa Sistemi Medicali is recalling seven Apollo DRF X-ray tables because the angulation chain may fail early due to metal fatigue.
Product
Apollo DRF, Model Number 9784220831 - Product Usage: The remote controlled table Apollo DRF is an X-ray equipment that allows to perform general radiographic and fluoroscopic examinations. The system is a fixed position type. The movements of the table and tube support are…
Category
Medical Device
Distribution
Distributed nationwide