State

New Mexico product recalls

73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

29651–29675 of 77373

SevereFDA (Drugs)·D-1351-2020·2020-07-01
Amneal Metformin Hydrochloride Extended-Release Tablets Recalled for NDMA Impurity
Amneal Pharmaceuticals is recalling Metformin Hydrochloride Extended-Release Tablets, 500 mg, because FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level.
Product
amneal Metformin Hydrochloride Extended-Release Tablets, 500 mg USP, 500 tablets bottles, Rx only, Distributed by: Amneal Pharmaceuticals LLC Bridgewater, NJ 08807 NDC 53746-0178-05
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1350-2020·2020-07-01
Amneal Metformin Hydrochloride Extended-Release Tablets Recalled for NDMA Impurity
Amneal Pharmaceuticals is recalling Metformin Hydrochloride Extended-Release Tablets because FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level.
Product
amneal Metformin Hydrochloride Extended-Release Tablets, USP, Bulk, Distributed by: Amneal Pharmaceuticals LLC Bridgewater, NJ 08807 NDC 53746-0178-BULK
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1352-2020·2020-07-01
Amneal Metformin Hydrochloride Extended-Release Tablets Recalled for NDMA Impurity
Amneal Pharmaceuticals is recalling Metformin Hydrochloride Extended-Release Tablets because FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level.
Product
amneal Metformin Hydrochloride Extended-Release Tablets, USP, 500 mg, 1000 tablets bottles, Distributed by: Amneal Pharmaceuticals LLC Bridgewater, NJ 08807 NDC 53746-0178-10
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1326-2020·2020-07-01
BIOTA Biosciences Recalls Sterile Cannabidiol Vials for Sterility Concerns
BIOTA Biosciences is recalling sterile Cannabidiol (CBD) vials due to lack of assurance of sterility and marketing without an approved NDA/ANDA.
Product
Sterile Cannabidiol (CBD) 4mg/mL, 10mL vial
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·20V381000·2020-07-01
Porsche Recalls 2020 911 Carrera 4S Coupe for Differential Bracket Issue
Porsche is recalling 2020 911 Carrera 4S Coupe vehicles because the front axle differential bracket may not be tightened correctly, potentially causing damage to surrounding components and increasing fire risk.
Product
PORSCHE — PORSCHE 911 CARRERA
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2404-2020·2020-07-01
Siemens Atellica IM1300 Analyzer Recall for Insufficient Sample Detection Failure
Siemens is recalling 927 Atellica Solution IM1300 Analyzers because they may fail to detect insufficient samples when using specific sample cups.
Product
Atellica Solution IM1300 Analyzer, Siemens Material Number 11066001, UDI # 00630414007960
Category
Medical Device
Distribution
44 states
HighFDA (Devices)·Z-2429-2020·2020-07-01
Suntech Oscar 2 Blood Pressure Monitor Recall for Display Error
Suntech Medical is recalling Oscar 2 blood pressure monitors because the display may show an incorrect decimal point for three-digit readings in mmHg.
Product
Oscar 2, Model 250 System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2425-2020·2020-07-01
Zest Anchors Recalls Locator Overdenture Implant Systems Due to Abutment Defects
Zest Anchors LLC is recalling Locator Overdenture Implant Systems because the abutments may be out of specification, potentially causing a gap between the implant and abutment.
Product
LOCATOR OVERDENTURE IMPLANT SYSTEM STERILE R Rx Only QTY 1 .
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·20V382000·2020-07-01
2020-2021 Forest River Vengeance Trailers Landing Leg Spacing Defect Recall
Forest River is recalling certain 2020-2021 Vengeance trailers because the fifth-wheel landing legs are not properly spaced, potentially allowing the fifth wheel to slip and puncture the trailer floor, increasing injury risk.
Product
FOREST RIVER — FOREST RIVER VENGEANCE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2418-2020·2020-07-01
Hocoma Lokomat Pro Recalled for Uncontrolled Body Weight Support Rope Movement
Hocoma AG is recalling 494 Lokomat Pro units because a motor controller failure may cause the body weight support rope to move up or down in an uncontrolled way.
Product
Lokomat Pro, Catalog Numbers 30003 LokomatPro L6.2 120V AD ; 30004 LokomatPro L6.2 120V Kombi; 30005 LokomatPro L6.2 120V PE; 30683 LokomatPro L6.2 110V FD PE; 30684 LokomatPro L6.2 110V FD Kombi; 32001 LokomatPro L6.2 110V FD AD Product Usage: The intended use of the…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2423-2020·2020-07-01
Tosoh AIA-900 Analyzer Recalled for Substrate Monitoring Defect
Tosoh Bioscience Inc is recalling 529 AIA-900 Analyzers because the substrate monitoring system may fail to detect empty bottles, leading to erroneous immunoassay test results.
Product
AIA-900 Analyzer, Part no. 022930, UDI 04560189283992
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2403-2020·2020-07-01
Merge Healthcare Software Recall for Inaccurate Z-Score Calculations
Merge Healthcare is recalling specific versions of Merge Cardio software due to a calculation error that may produce false negative Z-Scores.
Product
Merge Healthcare Merge Application Server Software Release and Merge Healthcare Merge Cardio Workstation Software Release - Product Usage: VERICIS is a system intended to be used to acquire, store, print, transfer, and archive clinical information from Camtronics and other…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·20V384000·2020-07-01
Volvo VNL and VNR Buses: Incorrect Axle Weight Rating Labels
Volvo is recalling certain 2018–2021 VNL and VNR buses with incorrect Gross Axle Weight Rating labels on rear drive axles. Overloading could cause wheel hub failure and increase the risk of a crash.
Product
VOLVO — VOLVO VNR, VNL
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1370-2020·2020-07-01
Aurobindo Recalls Clozapine Tablets Due to Foreign Tablet Presence
Aurobindo Pharma USA is recalling 1,440 bottles of Clozapine 100mg tablets because a consumer reported finding 50mg tablets in the 100mg bottles.
Product
CLOZAPINE — CLOZAPINE (CLOZAPINE)
Category
Drug
Distribution
Distributed nationwide
HighCPSC·20144·2020-07-01
Boy Scouts Recalls Cub Scout Activity Pins for Lead Content Violation
Boy Scouts of America is recalling Cub Scout activity pins because they contain lead levels exceeding federal safety limits.
Product
Cub Scout activity pins
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2405-2020·2020-07-01
Siemens Atellica Solution IM1600 Analyzer Recall for Sample Detection Issues
Siemens is recalling Atellica Solution IM1600 Analyzers because insufficient sample volumes may not be detected when using specific sample cups.
Product
Atellica Solution IM1600 Analyzer, Siemens Material Number 11066000, UDI # 00630414002026
Category
Medical Device
Distribution
44 states
HighFDA (Devices)·Z-2428-2020·2020-07-01
Providence Medical Technologies Recalls Ally Bone Screws Due to Dimensional Error
Providence Medical Technologies is recalling 208 units of Ally Bone Screws due to a potential dimensional manufacturing error that poses a safety risk to patients.
Product
Ally Bone Screw - Product Usage:Bone Screws are indicated for use in bone reconstruction, osteotomy, arthrodesis, joint fusion, fracture repair, and fracture fixation appropriate for the size of the device. Screws are intended for single use only. L Providence Medical…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1338-2020·2020-07-01
Crown Laboratories Recalls Subpotent Nystatin Cream Tubes
Crown Laboratories is recalling 62,274 tubes of Nystatin Cream because the product failed potency testing at the 9-month interval.
Product
NYSTATIN CREAM — NYSTATIN CREAM (NYSTATIN CREAM)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1341-2020·2020-07-01
Alembic Recalls Aripiprazole Tablets Due to Labeling Error
Alembic Pharmaceuticals is recalling aripiprazole tablets because bottles labeled as 2 mg contained 5 mg tablets. The error affects 19,153 bottles distributed nationwide.
Product
ARIPIPRAZOLE — ARIPIPRAZOLE (ARIPIPRAZOLE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2431-2020·2020-07-01
Siemens Atellica CH Chemistry Calibrator Recalled for Calibration Errors
Siemens Healthcare Diagnostics is recalling Atellica CH Chemistry Calibrators due to observed calibration errors in Total and Direct Bilirubin assays.
Product
Atellica CH Chemistry Calibrator
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1339-2020·2020-07-01
Crown Laboratories Recalls Nystatin Cream for Subpotent Drug Levels
Crown Laboratories is recalling Nystatin Cream, USP, because the product failed potency testing at the 9-month interval.
Product
NYSTATIN CREAM — NYSTATIN CREAM (NYSTATIN CREAM)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2430-2020·2020-07-01
Siemens ADVIA Chemistry Calibrator Recalled for Calibration Errors
Siemens Healthcare Diagnostics is recalling ADVIA Chemistry Calibrator lots 534177 and 534179 due to observed calibration errors in Total and Direct Bilirubin assays.
Product
ADVIA Chemistry Calibrator
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1337-2020·2020-07-01
Soft Whisper Dandruff Shampoo Recalled for Water Quality Deviations
A.P. Deauville, LLC is recalling Soft Whisper Dandruff Shampoo because it was produced with water that failed USP specifications.
Product
Soft Whisper by Powerstick Dandruff Shampoo (Pyrithione Zinc), 14.4 FL OZ. (426 mL), A.P. Deauville LLC New Brunswick, NJ 08901, NDC 42913-020-00, UPC 815195014097
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2427-2020·2020-07-01
Argon Medical Devices Recalls BioPince Biopsy Instruments Due to Labeling Error
Argon Medical Devices is recalling BioPince Full Core Biopsy Instruments because of incorrect product labeling. The recall affects 165 units in the U.S. and 330 units internationally.
Product
BioPince Full Core Biopsy Instrument 16ga x 15cm.,Use with Optional CO-Axial Needle MCXS1615BP. QTY.: 5/CS - Product Usage: The disposable, automatic BioPince Full Core Biopsy Instrument is used to obtain multiple core samples from soft tissue such as liver, kidney, abdominal…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1335-2020·2020-07-01
QuVa Pharma Recalls R.E.C.K. Syringes Due to Particulate Matter
QuVa Pharma is recalling 17,050 syringes of R.E.C.K. solution because they may contain particulate matter. The product was distributed nationwide in the US.
Product
R.E.C.K. (Ropivacaine, Epinephrine, Clonidine, Ketorolac) in Sodium Chloride solution 50 mL in 60 mL Syringe, Compounded by QuVa 519 Bloombury, NJ 08804, NDC 70092143350
Category
Drug
Distribution
Distributed nationwide