State

New Mexico product recalls

73,570 recalls have nationwide distribution and so reach New Mexico. 3,630 additional recalls listed New Mexico specifically in their distribution scope.

What the numbers show

Total: 3,630
Critical: 747
Severe: 813
Most recent: 2026-10-21

Of the 3,630 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 813 (22%) are Severe.

Which agencies issued them

These figures cover only the 3,630 recalls whose distribution notice names New Mexico specifically. The 73,570 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

23976–24000 of 77200

ModerateFDA (Drugs)·D-0017-2022·2021-10-27
Coppertone Pure & Simple Baby 50 Sunscreen Spray Recalled for cGMP Deviations
Beiersdorf Inc. is recalling 14,748 cans of Coppertone Pure & Simple baby 50 Sunscreen Spray due to cGMP (current Good Manufacturing Practice) deviations. The product was distributed nationwide.
Product
Coppertone Pure & Simple baby 50 Sunscreen Spray (To Deliver) Zinc Oxide 24.08%, NET WT 5 OZ (142 g) can, Beiersdorf Inc., Wilton, CT 06897 UPC 0 72140 02881 7
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0026-2022·2021-10-27
Omeprazole Magnesium Acid Reducer Capsules Recalled for Staple Contamination
Dr. Reddy's Laboratories is recalling Acid Reducer (Omeprazole Magnesium) 20 mg capsules nationwide because staples have been found co-mingled with capsules in bottles.
Product
ACID REDUCER — ACID REDUCER (OMEPRAZOLE MAGNESIUM)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0024-2022·2021-10-27
AirDuo Digihaler inhalation powder subpotent drug recall
Teva Pharmaceuticals is recalling AirDuo Digihaler 113/14 inhalation powder because some batches do not deliver the labeled amount of salmeterol, a critical active ingredient for asthma and COPD control.
Product
AirDuo Digihaler 113/14 (fluticasone propionate 113 mcg and salmeterol 14 mcg) Inhalation Powder, Rx Only, Mktd. by: Teva Respiratory, LLC, Frazer, PA 19355, Manufactured in Ireland, NDC 59310-129-06.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0151-2022·2021-10-27
HemosIL Liquid Anti-Xa Assay On-Board Stability Issue Recall
Instrumentation Laboratory is recalling HemosIL Liquid Anti-Xa, a coagulation assay measuring heparin activity, due to reduced on-board instrument stability from 7 days to 5 days.
Product
HemosIL Liquid Anti-Xa- Automated chromogenic assay for the quantitative determination of unfractionated heparin (UFH) and low molecular weight heparin (LMWH) activity in human citrated plasma on IL Coagulation Systems, (ACLTOP¿ Family, ACL TOP Family 50 Seriest and ACL…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0149-2022·2021-10-27
Heparin Activity Assay Labeling Correction: Reduced On-Board Stability
Instrumentation Laboratory is recalling HemosIL Liquid Anti-Xa kits due to a labeling correction. The on-board stability window has been reduced from 7 to 5 days.
Product
HemosIL Liquid Anti-Xa- Automated chromogenic assay for the quantitative determination of unfractionated heparin (UFH) and low molecular weight heparin (LMWH) activity in human citrated plasma on IL Coagulation Systems, (ACL TOP¿ Family, ACL TOP Family 50 Seriest and ACL…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0126-2022·2021-10-27
Plastic Tenaculum Surgical Instruments Recalled for Unconfirmed Manufacturing Standards
Stradis Medical is recalling plastic tenaculum surgical instruments because the manufacturer cannot confirm they were produced in accordance with required design and manufacturing standards. Approximately 2,483 kits were distributed nationwide and to Canada.
Product
Tenaculum, Plastic
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0021-2022·2021-10-27
AirDuo Digihaler 113/14 Inhalation Powder Subpotent Drug Recall
Teva Pharmaceuticals is recalling AirDuo Digihaler 113/14 inhalation powder because some units contain less salmeterol than the labeled dose. The affected sample batch was distributed nationwide.
Product
AirDuo Digihaler 113/14 (fluticasone propionate 113 mcg and salmeterol 14 mcg) Inhalation Powder, Sample Not For Sale, Rx Only, Mktd by: Teva Respiratory, LLC , Frazer, PA 19355, Manufactured in Ireland, NDC 59310-520-08
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0027-2022·2021-10-27
Lupin Imipramine Pamoate Capsules Recalled for Failed Dissolution Test
Lupin Pharmaceuticals is recalling approximately 1,902 bottles of Imipramine Pamoate Capsules 125 mg due to out-of-specification results in dissolution testing at the 9-month stability checkpoint.
Product
IMIPRAMINE PAMOATE — IMIPRAMINE PAMOATE (IMIPRAMINE PAMOATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0016-2022·2021-10-27
Coppertone Pure & Simple Kids 50 Sunscreen Spray Recalled for cGMP Deviations
Beiersdorf Inc. is voluntarily recalling Coppertone Pure & Simple kids 50 Sunscreen Spray due to current Good Manufacturing Practice (cGMP) deviations. The recall affects 70,320 cans distributed nationwide.
Product
Coppertone Pure & Simple kids 50 Sunscreen Spray (To Deliver) Zinc Oxide 24.08%, NET WT 5 OZ (142 g) can, Beiersdorf Inc., Wilton, CT 06897 UPC 0 72140 02882 4
Category
Drug
Distribution
Distributed nationwide
ModerateCPSC·22008·2021-10-27
5.11 Tactec Plate Carriers Recalled Due to Injury Hazard
5.11 Inc. is recalling about 45,170 Tactec Plate Carriers (style 56100) because the cable in the quick release system can separate from the handle, preventing swift removal in an emergency. No injuries have been reported.
Product
56100 Tactec™ Plate Carriers
Category
Consumer Product
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0020-2022·2021-10-27
GlipiZIDE Extended-Release Tablets 2.5 mg Nationwide Recall
American Health Packaging is recalling GlipiZIDE Extended-Release Tablets 2.5 mg (Lot #194141) nationwide because dissolution test results exceeded specification, which may affect the drug's effectiveness.
Product
GlipiZIDE Extended-Release Tablets, 2.5 mg, 30 Tablets (3 blister cards each with 10 individually blistered doses), Rx only, Manufactured by: Patheon Pharmaceuticals Inc., Cincinnati, OH 45237; Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054. Carton NDC#…
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·21V839000·2021-10-26
Nissan Recalls 2017-2019 Rogue Hybrid Vehicles for Engine Harness Defect
Nissan is recalling 2017-2019 Rogue Hybrid vehicles because contact with the ECM bracket may damage the engine harness, causing a blown fuse and potential engine stall.
Product
NISSAN — NISSAN ROGUE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21E090000·2021-10-26
WABCO Trailer ABS Systems Recalled for Brake Pressure Loss Risk
WABCO is recalling certain Trailer ABS Systems because improperly tightened screws may loosen, causing pressure loss and potential brake failure.
Product
SERVICE BRAKES, AIR recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V837000·2021-10-25
2020-2023 IC Bus School Buses Recalled for Engine Shut Down Risk
Navistar is recalling 2020-2023 IC Bus CESB school buses due to an engine control module defect that may cause unexpected engine shutdown while driving, increasing the risk of crashes and emergency evacuation situations.
Product
IC BUS — IC BUS CESB
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V835000·2021-10-25
Tesla Model 3 and Model Y suspension fasteners recalled for loosening
Tesla is recalling 2019-2021 Model 3 and 2020-2021 Model Y vehicles where front suspension lateral link fasteners may loosen, potentially causing wheel misalignment and increasing crash risk.
Product
TESLA — TESLA MODEL 3, MODEL Y
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V834000·2021-10-25
2020-2023 Tesla Model 3 Curtain Airbag Deployment Safety Defect
Tesla is recalling certain 2020-2023 Model 3 vehicles because the side curtain airbag may be improperly secured to the roof rail and could twist, deploying incorrectly during a crash and increasing risk of injury or ejection.
Product
TESLA — TESLA MODEL 3
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V838000·2021-10-25
Navistar Recalls 2020-2021 IC CE Buses for Engine Shutdown Risk
Navistar is recalling 2020-2021 IC CE transit buses because a software fault may cause unexpected engine shutdowns, increasing crash risk.
Product
IC BUS — IC BUS CE
Category
Vehicle
Distribution
Distributed nationwide
ModerateNHTSA·21V836000·2021-10-25
Yamaha Recalls 2021 Tracer 9 GT for Incorrect VIN Label
Yamaha is recalling 2021 Tracer 9 GT motorcycles because the VIN on the certification label may not match the vehicle's stamped VIN, potentially preventing owners from receiving safety recall remedies.
Product
YAMAHA — YAMAHA TRACER 9 GT
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V833000·2021-10-23
Ferrari Recalls 458 and 488 Models for Brake Fluid Leak Risk
Ferrari is recalling specific 458 and 488 models because the brake system may leak fluid, potentially causing a loss of braking ability.
Product
FERRARI — FERRARI 488 GTB, 458 ITALIA, 488 SPIDER, 458 SPECIALE
Category
Vehicle
Distribution
Distributed nationwide
CriticalCPSC·22007·2021-10-22
Walmart Better Homes and Gardens Room Spray Recalled for Dangerous Bacteria
Walmart is recalling Better Homes and Gardens Essential Oil Infused Aromatherapy Room Spray with Gemstones due to contamination with Burkholderia pseudomallei bacteria. CDC testing identified the hazard and is investigating a cluster of four melioidosis cases, including two deaths.
Product
Better Homes and Gardens Essential Oil Infused Aromatherapy Room Spray with Gemstones
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·21V830000·2021-10-22
2021-2022 Forest River XLR Toy Hauler Recalled for Missing Furnace Protective Panel
Forest River is recalling certain 2021-2022 XLR Toy Hauler recreational vehicles with a missing protective panel between the furnace and cargo area. The missing panel could allow cargo to contact furnace wiring, creating a fire hazard.
Product
FOREST RIVER — FOREST RIVER XLR TOYHAULER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V828000·2021-10-22
2022 Coachmen Catalina Travel Trailer Recall for Unsealed Furnace Panel
Forest River is recalling 2022 Coachmen Catalina travel trailers because an unsealed panel between the furnace and cooktop could cause an inverted flame, increasing fire risk.
Product
COACHMEN — COACHMEN CATALINA
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V829000·2021-10-22
2022 Forest River XLR Toy Hauler Recalled for Electrical Fire Risk
2022 Forest River XLR Toy Hauler RVs are recalled due to incorrect wiring lacking required over-current protection. The defect can cause electrical shorts and fire; dealers will replace the wiring and breaker at no cost.
Product
FOREST RIVER — FOREST RIVER XLR TOYHAULER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V832000·2021-10-22
Mercedes-Benz Recalls 2021 Models for Rear Window Bonding Defect
Mercedes-Benz is recalling certain 2021 GLE and GLS models because the rear window may be insufficiently bonded, posing a road hazard risk.
Product
MERCEDES-BENZ — MERCEDES-BENZ GLS450, AMG GLE53, GLS580, GLE 580
Category
Vehicle
Distribution
Distributed nationwide
ModerateNHTSA·21V831000·2021-10-22
2022 BMW X4 Rear License Plate Lamp Illumination Defect
BMW is recalling certain 2022 X4 vehicles because the rear license plate may not be properly illuminated, violating federal safety standards and potentially creating visibility issues for other drivers.
Product
BMW — BMW X4
Category
Vehicle
Distribution
Distributed nationwide