State

New Mexico product recalls

72,940 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 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

2101–2125 of 76565

ModerateFDA (Drugs)·D-0505-2026·2026-05-06
Fentanyl Citrate Injectable Solution Recalled for cGMP Deviations
Wells Pharma of Houston LLC has recalled fentanyl citrate injectable solution (1250 mcg/25mL) distributed nationwide due to cGMP deviations. The recall involves 50 syringes from Lot 011226204250063, expiring 05/14/2026.
Product
fentaNYL Citrate Injectable Solution, Narcotic, CII, 1250 mcg/25mL (50 mcg per mL), 25 mL, wells pharma of Houston, NDC 73702-204-25.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0503-2026·2026-05-06
Fentanyl Citrate Injectable Solution Recalled for cGMP Deviations
Wells Pharma is recalling fentanyl citrate injectable solution (1000 mcg/100 mL, 10 mcg per mL) distributed nationwide due to current good manufacturing practice (cGMP) deviations. The recall affects 4,030 IV bags with various lot numbers and expiration dates between April and June 2026.
Product
fentaNYL Citrate Injectable Solution, NARCOTIC, Cii, 1000 mcg/100 mL (10 mcg per mL), 100 mL bag, Wells Pharma in Houston, NDC 73702-202-02.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1964-2026·2026-05-06
Philips MR 7700 MR Elastography device stiffness value error recall
Philips is recalling certain MR 7700 devices with MR Elastography due to potential stiffness value errors when specific image reconstruction parameters are used, which may cause voxel size settings to display incorrectly.
Product
Philips MR 7700 with MR Elastography (MRE). 1. Model Number (REF): 782120. 2. Model Number (REF): 782153.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1968-2026·2026-05-06
Philips SmartPath to Ingenia Elition X MR Elastography Stiffness Value Errors
Philips is recalling three models of SmartPath to Ingenia Elition X with MR Elastography devices due to potential stiffness value errors when specific image reconstruction parameters are combined with Resoundant's algorithm.
Product
Philips SmartPath to Ingenia Elition X with MR Elastography (MRE). 1. Model Number (REF): 782118. 2. Model Number (REF): 782144. 3. Model Number (REF): 782163.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1988-2026·2026-05-06
DePuy Synthes ATTUNE Revision Hinge Femoral Component Sterility Recall
DePuy Synthes is recalling 3 units of ATTUNE REVISION HINGE FEMORAL LT SZ 8 CEM due to external sterile packaging adhered to internal packaging, potentially compromising sterility.
Product
Depuy Synthes, ATTUNE REVISION HINGE FEMORAL LT SZ 8 CEM. Part Number: 150450108.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1969-2026·2026-05-06
Philips MR 7700 MRE Upgrade MRI Equipment Stiffness Value Error Risk
Philips is recalling 15 units of its MR 7700 with MR Elastography upgrade due to potential stiffness value errors in MRI scans when specific image reconstruction parameters are used with the Resoundant algorithm.
Product
Philips Upgrade to MR 7700 with MR Elastography (MRE). 1. Model Number (REF): 782130.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0507-2026·2026-05-06
Ketamine Hydrochloride Injectable Solution Recalled for cGMP Deviations
Wells Pharma of Houston LLC is recalling 4,975 syringes of Ketamine Hydrochloride Injectable Solution (50 mg/mL) distributed nationwide due to current Good Manufacturing Practice (cGMP) deviations.
Product
Ketamine Hydrochloride Injectable Solution, 50mg/ml, (50 mg per mL) Volume: 1 mL, 5265 Kitty Drive, Houston, TX 77054, NDC 73702-302-31.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2004-2026·2026-05-06
Philips Bridge Prep Kit catheter may experience resistance during advancement
Merit Medical Systems, Inc. is recalling the Philips Bridge Prep Kit (Ref K12-09098C) because the catheter may experience resistance when being advanced over the guidewire during use.
Product
Philips Bridge Prep Kit REF: K12-09098C Sterile EO, Rx ONLY
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0509-2026·2026-05-06
CVS Lidocaine Wound Gel recalled for failed pH specifications
CVS Lidocaine Wound Gel is being recalled because it failed pH specifications. The affected product is distributed nationwide.
Product
Lidocaine Wound Gel (Benzalkonium Chloride, 0.13% and Lidocaine Hydrochloride, 2%), NET WT 0.5 OZ (14 g), Distributed by: CVS PHarmacy, INc., One CVS Drive, Woonsocket, RI 02895. NDC 59898-950
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1998-2026·2026-05-06
Heraeus PALAMIX duo dental mixing system batches worldwide recall
Heraeus Medical is recalling PALAMIX duo dental mixing units (Material Number 66057897) because the mixing rod may come loose from its lock during use in units older than 1.5 years. The shelf life is being reduced from 3 years to 1.5 years.
Product
Heraeus, PALAMIX duo. Material Number: 66057897.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0494-2026·2026-05-06
Levocarnitine Injection USP Missing Label Recall
American Regent, Inc. is recalling Levocarnitine Injection USP (1 g/5 mL) due to missing labeling on certain lots. The affected product was distributed nationwide.
Product
LEVOCARNITINE — LEVOCARNITINE (LEVOCARNITINE)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1997-2026·2026-05-06
Heraeus PALAMIX uno Dental Material Mixing Rod Loose Risk Recall
Heraeus Medical is recalling PALAMIX uno dental material because the mixing rod may come loose during mixing in units older than 1.5 years. The shelf life has been reduced from 3 years to 1.5 years.
Product
Heraeus, PALAMIX uno. Material Number: 66057893.
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·26V285000·2026-05-05
Winnebago Recalls 2026-2027 Solis RVs Due to LP Hose Routing Defect
Winnebago is recalling 2026-2027 Solis recreational vehicles because the liquid propane hose may be routed over the exhaust heat shield, posing a fire risk.
Product
WINNEBAGO — WINNEBAGO SOLIS
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V284000·2026-05-05
Utilimaster Velocity Recalled for Incorrect Cargo Capacity Label
Shyft Group is recalling 2025 Utilimaster Velocity vehicles because the cargo carrying capacity label may list an incorrect load value, potentially leading to overloading.
Product
UTILIMASTER — UTILIMASTER VELOCITY
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V283000·2026-05-04
Tesla rearview camera image may be delayed when reverse is selected
Tesla is recalling certain vehicles running software version 2026.8.6 because the rearview camera image may be delayed when the vehicle is placed in reverse, breaching FMVSS 111.
Product
TESLA — TESLA MODEL 3, MODEL X, MODEL Y, MODEL S
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V282000·2026-05-04
2026 Toyota 4Runner Vehicles Recalled Due to Incorrect Load Capacity Label
Gulf States Toyota, Inc. is recalling certain 2026 Toyota 4Runner vehicles because the load carrying capacity label is incorrect. This error may lead to improper vehicle loading and increase the risk of a crash.
Product
TOYOTA — TOYOTA 4RUNNER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V281000·2026-05-01
Mercedes-Benz vehicles recalled over instrument panels that go blank
Mercedes-Benz USA is recalling 144,049 vehicles because the infotainment control unit may reset while the vehicle is in motion and cause the instrument panel display to go blank.
Product
MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES-MAYBACH GLC 300, GLC 300 4MATIC, C 300 4MATIC, E 450 4MATIC
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V279000·2026-05-01
New Flyer Recalls 2022 XE40 Buses for Speedometer Illumination Defect
New Flyer is recalling 2022 XE40 transit buses because the speedometer may not illuminate when headlights are on, increasing crash risk.
Product
NEW FLYER — NEW FLYER XE40
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26E026000·2026-05-01
Waymo Recalls 5th and 6th Generation Automated Driving Systems for Water Hazard
Waymo is recalling 3,791 automated driving systems because software may allow vehicles to drive into standing water, increasing crash risk.
Product
ELECTRICAL SYSTEM:ADAS:AUTONOMOUS/SELF DRIVING:SOFTWARE recall
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V280000·2026-05-01
2026 Ram ProMaster Recalled for Incomplete Rear Seat Assembly
Braun Corporation is recalling 2026 Ram ProMaster vehicles because the rear bench seat may be missing two legs, which could fail to restrain occupants in a crash.
Product
RAM — RAM PROMASTER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V278000·2026-05-01
Mercedes-Benz Recalls 2026 CLA EVs for Seat Belt Retractor Defect
Mercedes-Benz is recalling 2026 CLA 350 4MATIC and CLA 250+ EVs because the front passenger seat belt may remain locked, preventing proper restraint in a crash.
Product
MERCEDES-BENZ — MERCEDES-BENZ CLA 250+ (EV), CLA 350 4MATIC (EV)
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26V276000·2026-04-30
Grand Design Lineage solar panels may detach from the roof
Grand Design is recalling certain 2025-2026 Lineage recreational vehicles because the adhesive securing the roof solar panels may fail, allowing a panel to detach into the roadway.
Product
GRAND DESIGN — GRAND DESIGN LINEAGE
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·26456·2026-04-30
Boo Bunnie toy cubes can break into small parts and sharp edges
Stephan Baby Boo Bunnie and Friends toys are recalled after 20 reports of the water-filled cube cracking or breaking, including one case where a child swallowed sharp pieces.
Product
Stephan Baby Boo Bunnie and Friends Children's Toys
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·26444·2026-04-30
Thermos food jar stoppers can eject forcefully and cause eye injuries
Thermos Stainless King food jars and Sportsman bottles are recalled after 27 reports of stoppers ejecting forcefully on opening, including three consumers with permanent vision loss.
Product
Thermos Stainless King 3000 and 3020 Food Jars and Thermos Sportsman 3010 Food & Beverage Bottles
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·26V275000·2026-04-30
Nova Bus LFS transit buses may lose drive power from data overload
Nova Bus is recalling certain 2022-2023 LFS transit buses because a telemetry control unit may cause a data overload, shutting down the unit and causing a loss of drive power.
Product
NOVA BUS — NOVA BUS LFS
Category
Vehicle
Distribution
Distributed nationwide