State

New Mexico product recalls

72,969 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 72,969 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

3976–4000 of 76594

ModerateFDA (Devices)·Z-0894-2026·2025-12-17
Sacroiliac fusion screws recalled over labeling claims not consistently present
Orthofix U.S. is recalling 19,431 FIREBIRD SI Fusion System units because the labeling contains claims that are not consistently present.
Product
Brand Name: FIREBIRD" SI Fusion System Product Name: FIREBIRD" SI Fusion System Model/Catalog Number: 18-1025SP 11mm X 25mm FIREBIRD SI Screw; 18-1030SP 11mm X 30mm FIREBIRD SI Screw; 18-1035SP 11mm X 35mm FIREBIRD SI Screw; 18-1040SP 11mm X 40mm FIREBIRD SI Screw; 18-1045S
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0908-2026·2025-12-17
Ureteral stent kits, 8 French, recalled over a size labeling discrepancy
C.R. Bard is recalling 116 BD InLay Optima Ureteral Stent Kits, 8 Fr x 26 cm, because the actual stent size may not match the product label.
Product
BD InLay Optima Ureteral Stent Kit Size: 8 Fr. x 26 cm, Ureteral Stent Kit REF 78826
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0895-2026·2025-12-17
Titanium spacer implants recalled over labeling claims not consistently present
Orthofix U.S. is recalling 14,201 Forza Ti Spacer System units because the labeling contains claims that are not consistently present.
Product
Brand Name: Forza" Ti Spacer System Product Name: Forza" Ti Spacer System Model/Catalog Number: 38-2006SP FORZA Ti Spacer, Straight, 0¿, 9W x 23L x 6H; 38-2007SP FORZA Ti Spacer, Straight, 0¿, 9W x 23L x 7H; 38-2008SP FORZA Ti Spacer, Straight, 0¿, 9W x 23L x 8H; 38-2009SP F
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0221-2026·2025-12-17
Compounded ophthalmic syringes recalled over an incorrect product formulation
Fagron Compounding Services is recalling 2,980 syringes of a compounded topical ophthalmic solution over an incorrect product formulation.
Product
Tropicamide 1%/Cyclopentolate 1%/Phenylephrine 2.5%/Ketorolac 0.5% Topical Ophthalmic Solution, 0.5mL Single-Use Syringe, For Topical Ophthalmic Use Only. Not for IV Use. Fagron Sterile Services, 8710 E 34th St N, Wichita, KS 67226. NDC: 71266-8240-01
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0912-2026·2025-12-17
Hemodialysis systems recalled because a screw may loosen or fall out
Nipro Medical is recalling Surdial DX Hemodialysis Systems because a screw may loosen or fall out of the system.
Product
Hemodialysis System, Surdial DX REF: MC+SDX01 Rx Only
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0223-2026·2025-12-17
Morphine sulfate oral solution recalled over a carton size mismatch
Winder Laboratories is recalling 3,528 bottles of Morphine Sulfate Oral Solution because the size stated on the carton label did not match the size of the bottle inside.
Product
MORPHINE SULFATE — MORPHINE SULFATE (MORPHINE SULFATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0896-2026·2025-12-17
Titanium spinal spacers recalled over labeling claims not consistently present
Orthofix U.S. is recalling 40,956 CONSTRUX Mini Ti Spacer System units because the labeling contains claims that are not consistently present.
Product
Brand Name: CONSTRUX" Mini Ti Spacer System Product Name: CONSTRUX" Mini Ti Spacer System Model/Catalog Number: 37-6005SP 12mm W X 12mm L, 5mm H, 5¿ Lordotic 37-6005SP 12mm W X 12mm L, 5mm H, 5¿ Lordotic 37-6005SP 12mm W X 12mm L, 5mm H, 5¿ Lordotic 37-6006SP 12mm W X 12
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0897-2026·2025-12-17
Chemotherapy gowns recalled over an expiration date printed two years late
Cardinal Health is recalling 251,165 ChemoPlus gowns and sleeves because the packaging shows a five-year shelf life when the product's actual shelf life is three years.
Product
ChemoPlus gowns: Product Code Product Description CT5500T ChemoPlus Full Coverage Sleeve, Universal, Medium Blue, Non-sterile; CT5502T ChemoPlus Full Coverage Gown, Closed Back, Regular/Medium, Medium Blue, Non-sterile; CT5503T ChemoPlus Full Coverage Gown, Closed Back, Large
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0907-2026·2025-12-17
Ureteral stent kits recalled because the stent size may not match the label
C.R. Bard is recalling 116 BD InLay Optima Ureteral Stent Kits, 6 Fr x 30 cm, because the actual stent size may not match the product label.
Product
BD InLay Optima Ureteral Stent Kit Size: 6 Fr. x 30 cm, Ureteral Stent Kit REF 788630
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0227-2026·2025-12-17
Sertraline tablets recalled because bottle seals are not adhering
Lupin Pharmaceuticals is recalling 52,128 bottles of Sertraline Hydrochloride Tablets, 100 mg, over a defective container in which the seal is not adhering to the bottles.
Product
SERTRALINE HYDROCHLORIDE — SERTRALINE HYDROCHLORIDE (SERTRALINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0905-2026·2025-12-17
Short ureteral stent kits recalled over a size labeling discrepancy
C.R. Bard is recalling 116 Bard InLay Optima Ureteral Stent Kits, 6 Fr x 14 cm, because the actual stent size may not match the product label.
Product
Bard InLay Optima Size: 6 Fr. x 14 cm, Ureteral Stent Kit REF 787614
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0219-2026·2025-12-17
Varenicline tablets recalled after an assay value fell below specification
Dr. Reddy's Laboratories is recalling 4,800 bottles of Varenicline Tablets, 1mg, after the assay value for the affected lot fell below the specification limit at nine-month stability testing.
Product
VARENICLINE TARTRATE — VARENICLINE TARTRATE (VARENICLINE TARTRATE)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0917-2026·2025-12-17
Balloon pump systems recalled with a revised preventative maintenance schedule
Datascope is recalling 47 Cardiosave Rescue Intra-Aortic Balloon Pump systems to issue an instructions for use addendum revising the preventative maintenance schedule.
Product
Cardiosave Rescue. Intra-Aortic Balloon Pump system.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0916-2026·2025-12-17
Hybrid balloon pumps recalled with a revised preventative maintenance schedule
Datascope is recalling 11,470 Cardiosave Hybrid Intra-Aortic Balloon Pump systems to issue an instructions for use addendum revising the preventative maintenance schedule.
Product
Cardiosave Hybrid. Intra-Aortic Balloon Pump system.
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·25V869000·2025-12-16
Toyota hybrid inverter bolt can loosen causing power loss or fire
Toyota is recalling certain 2025-2026 Camry Hybrid and 2026 Corolla Cross Hybrid vehicles because a bolt inside the inverter may not be tightened properly, causing incomplete contact at the terminal.
Product
TOYOTA — TOYOTA CAMRY HYBRID, COROLLA CROSS HYBRID
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V870000·2025-12-16
Gillig Recalls 2025 Low Floor Buses Due to Wheelchair Restraint Defect
Gillig is recalling 2025 Low Floor transit buses because wheelchair restraints may fail to lock, posing an injury risk.
Product
GILLIG — GILLIG LOW FLOOR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V867000·2025-12-15
Mack Trucks Recalls 2010-2016 Granite Trucks Due to Brake Imbalance Risk
Mack Trucks is recalling 2010-2016 Granite trucks because incorrect parts from a previous repair may cause brake overheating, increasing the risk of tire blowouts or fires.
Product
MACK — MACK GRANITE (GU)
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V868000·2025-12-15
Gillig Recalls 2013 Low Floor Transit Buses for Emergency Exit Defect
Gillig is recalling 2013 Low Floor transit buses because emergency exit window latches may fail during a crash, increasing injury risk.
Product
GILLIG — GILLIG LOW FLOOR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V860000·2025-12-12
Ford Recalls 2022-2025 E-Transit Vehicles Due to Axle Shaft Defect
Ford is recalling 2022-2025 E-Transit vehicles because the left rear axle half shaft may disengage, causing loss of drive power or vehicle rollaway.
Product
FORD — FORD E-TRANSIT
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V866000·2025-12-12
Ford Super Duty trucks recalled over rear axle shafts that may break
Ford is recalling 6,819 model year 2026 Super Duty F-250 and F-350 vehicles because the right rear axle shaft may have been improperly heat-treated and may break.
Product
FORD — FORD F-350 SD, F-250 SD
Category
Vehicle
Distribution
Distributed nationwide
SevereUSDA FSIS·038-2025·2025-12-12
Suzanna's Kitchen Recalls Breaded Chicken for Undeclared Soy Allergen
Suzanna's Kitchen is recalling fully cooked breaded chicken products because they contain soy, a known allergen, that is not declared on the label.
Product
Suzanna's Kitchen — Suzanna’s Kitchen Recalls Fully Cooked Breaded Chicken Products Due to Misbranding and an Undeclared Allergen
Category
Food
Distribution
Distributed nationwide
HighNHTSA·25V865000·2025-12-12
Mercedes-Benz wagons recalled over wiring harness routing near the front driveshaft
Mercedes-Benz USA is recalling 117 AMG E 53 4MATIC+ Wagon vehicles because the transmission wiring harness may be routed too close to the front driveshaft, which can cause a loss of drive power.
Product
MERCEDES-BENZ — MERCEDES-BENZ AMG E 53 4MATIC+ WAGON
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V864000·2025-12-12
Mercedes-Benz GLE vehicles recalled over rear seat belts lacking child seat locking
Mercedes-Benz USA is recalling 82 model year 2025-2026 GLE 350 4MATIC vehicles because center rear seat belts may have been installed without the child seat protection function.
Product
MERCEDES-BENZ — MERCEDES-BENZ GLE 350 4MATIC
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V861000·2025-12-12
Diamond Coach VIP Buses Recalled for Wheelchair Restraint Defect
Diamond Coach is recalling 2025 VIP buses because wheelchair restraints may fail to lock, increasing injury risk during transit.
Product
DIAMOND COACH — DIAMOND COACH VIP
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V862000·2025-12-12
Ford Recalls 2025-2026 Corsair and Escape for Seat Belt Defect
Ford is recalling 2025-2026 Corsair and Escape vehicles because rear seat belt retractors may not be securely fastened, increasing injury risk in crashes.
Product
FORD — FORD, LINCOLN ESCAPE, CORSAIR
Category
Vehicle
Distribution
Distributed nationwide