The Recall Desk

State

New Mexico product recalls

72,968 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 72,968 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

3651–3675 of 76593

  • HighFDA (Devices)·Z-1057-2026·2026-01-21

    Levothyroxine tablets recalled after a bottle held the wrong strength

    Alvogen is recalling a lot of Levothyroxine Sodium Tablets, 150mcg, after a pharmacy reported a single bottle containing 88 mcg tablets instead of 150 mcg tablets.

    Product
    Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) PRE OP KIT, Medline kit SKU DYKS1093B; 2) PRE OP KIT, Medline kit SKU DYKS1124C; 3) PRE OP KIT, Medline kit SKU DYKS1128C; 4) PREOP KIT, Medline kit SKU DYKS1130B; 5) P
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1078-2026·2026-01-21

    Oncology information system recalled over a potential for overtreatment

    Elekta is recalling a MOSAIQ Oncology Information System with Particle Therapy License because a specific sequence can result in a partial treatment being delivered twice.

    Product
    MOSAIQ Oncology Information System with Particle Therapy License (License Kit 45700000000IQRO)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0262-2026·2026-01-21

    Aleve recalled over insanitary conditions at a distribution center

    Gold Star Distribution is recalling Aleve over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.

    Product
    Aleve 1's, 60 CT
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0281-2026·2026-01-21

    Ice gel recalled over insanitary conditions at a distribution center

    Gold Star Distribution is recalling Personal Care Ice Gel over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.

    Product
    Personal Care, Ice Gel, 8oz, 12 count, UPC 048155903463
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0282-2026·2026-01-21

    Carmex lip balm recalled over insanitary conditions at a distribution center

    Gold Star Distribution is recalling Carmex over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.

    Product
    Carmex a) jar, 12 count, UPC: 083078123154, 083078113155; b) Tube, PEG, 12 count, UPC: 083078123147, 083078113148
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0261-2026·2026-01-21

    Frozen raw shrimp recalled over elevated levels of chloramphenicol

    AZ Gems is recalling 1,099 cases of Member's Mark Jumbo Raw Shrimp over elevated levels of chloramphenicol.

    Product
    Advil a) Ibuprofen, Dispenser Pack, 2 tablet packets in box containing 50 individual packets, UPC: 305730154895; b) PM, Ibuprofen, Dispenser Pack, 2 Caplet packets in box containing 50 packets, UPC: 305730164559
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0263-2026·2026-01-21

    Alka Seltzer recalled over insanitary conditions at a distribution center

    Gold Star Distribution is recalling Alka Seltzer over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.

    Product
    Alka Seltzer, a) Original, 2 tablets per packet in 58 count box, UPC: 815556020033, 016500514473, b) Plus Cold & Flu, 2 tablets per packet in 36 count box, UPC: 016500594932
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0269-2026·2026-01-21

    Excedrin recalled over insanitary conditions at a distribution center

    Gold Star Distribution is recalling Excedrin over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.

    Product
    EXCEDRIN 2'S DISP.- 30 CT
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1051-2026·2026-01-21

    Pre-op kits recalled because they contain recalled B. Braun administration sets

    Medline is recalling 32 units of kits containing B. Braun IV administration sets, which were recalled because check valve components may become stuck in the open or closed positions.

    Product
    Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) DELUXE PRE OP KIT, Medline SKU DYKS2034A; 2) DELUXE PRE OP KIT, Medline SKU DYKS2006B.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1050-2026·2026-01-21

    Open heart kits recalled because they contain recalled B. Braun administration sets

    Medline is recalling 633 units of kits containing B. Braun IV administration sets, which were recalled because check valve components may become stuck in the open or closed positions.

    Product
    Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) OPEN HEART ACCESSORY CDSKit SKU CDS984289O; 2) OPEN HEART CDSKit SKU CDS984355K; 3) BAG A OPEN HEART KITKit SKU DYKM1025D; 4) RR-CABG SUPPLEMENTAL PACKKit SKU DYNJ0394752
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0259-2026·2026-01-21

    Carotid anesthesia kits recalled over recalled B. Braun administration sets inside

    Medline is recalling 10 units of kits containing B. Braun IV administration sets, which were recalled because check valve components may become stuck in the open or closed positions.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1017-2026·2026-01-21

    Allura Xper FD20 systems recalled over a missing cooling unit drip tray

    Philips Medical Systems Nederland is recalling 79 units of the Allura Xper FD20, model 722012, because the drip tray beneath the cooling unit may not have been installed.

    Product
    VANTAGE GALAN 3T Model MRT-3020/MEXL-3020
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1065-2026·2026-01-21

    Allura Xper FD10/10, model 722005, recalled over a missing drip tray

    Philips Medical Systems Nederland is recalling 14 units of the Allura Xper FD10/10, model 722005, because the drip tray beneath the cooling unit may not have been installed.

    Product
    Allura Xper FD10/10; Model Number: 722005;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1088-2026·2026-01-21

    Robotic and gynaecology kits recalled over leaking suction irrigators inside

    Medline is recalling 12,584 procedure convenience kits containing Stryker Strykeflow 2 Suction Irrigators, which can leak or emit vaporized saline during use.

    Product
    Medline medical procedure convenience kits labeled as: 1) ROBOTIC, REF CDS980523M; 2) ROBOTIC GYN, REF CDS980647K; 3) DAVINCI PROCEDURE, REF CDS980864Q; 4) GYN-URO LAPSCP CDS-LF, REF CDS981583U; 5) GYN-URO LAPSCP CDS-LF, REF CDS981583V; 6) GYN ROBOTIC, REF CDS981826K
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1086-2026·2026-01-21

    Laparoscopy kits recalled over suction irrigators that can leak during use

    Medline is recalling 41,432 laparoscopy convenience kits containing Stryker Strykeflow 2 Suction Irrigators, which can leak or emit vaporized saline during use.

    Product
    Medline medical procedure convenience kits labeled as: 1) LAPAROSCOPY CDS-LF, REF CDS860235L; 2) GENERAL LAPAROSCOPIC, REF CDS930223M; 3) LAP CHOLE CDS, REF CDS983678K; 4) LAPAROSCOPY PELV CDS, REF CDS983679K; 5) LAP CHOLE CDS-LF, REF CDS983752M; 6) LAP CHOLE CDS-LF,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1038-2026·2026-01-21

    Universal implant inserters recalled because the rotation tool handle can untread

    Medicrea International is recalling 44 IB3D Universal Implant Inserters because, following complaints, the orthopedic rotation tool handle may untread from the shaft.

    Product
    Medicrea, IB3D Universal Implant Inserter, Rx Only REF: A24000000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1043-2026·2026-01-21

    Neurostimulator clinician programmer app recalled over faults during device use

    Medtronic is recalling 7,123 units of the Vanta Clinician Programmer Application after complaints that it does not function as intended during use.

    Product
    A71200 Vanta" Clinician Programmer Application (CP App) version 2.0.2465 and 2.0.2683, Product number A71200. Software is deployed and operated on Samsung tablets (CFN CT900).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1075-2026·2026-01-21

    Allura Xper FD20, model 722028, recalled over a missing drip tray

    Philips Medical Systems Nederland is recalling 2 Allura Xper FD20 systems because the drip tray beneath the cooling unit may not have been installed.

    Product
    Allura Xper FD20; Model Number: 722028;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1090-2026·2026-01-21

    Robotic prostate kits recalled over suction irrigators that can leak

    Medline is recalling 12 units of procedure convenience kits containing Stryker Strykeflow 2 Suction Irrigators, which can leak or emit vaporized saline during use.

    Product
    Medline medical procedure convenience kits labeled as: KIT ROBOTICS UROLOGY PROSTATE, REF DYKMBNDL116G
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1054-2026·2026-01-21

    Facial procedure packs recalled over recalled B. Braun administration sets inside

    Medline is recalling 16 units of kits containing B. Braun IV administration sets, which were recalled because check valve components may become stuck in the open or closed positions.

    Product
    Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: DR HOLCOMB FACIAL PACK, Medline kit SKU DYNJ54488A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1055-2026·2026-01-21

    IV supply drawers recalled over recalled B. Braun administration sets inside

    Medline is recalling 3045 units of kits containing B. Braun IV administration sets, which were recalled because check valve components may become stuck in the open or closed positions.

    Product
    Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) DRAWER 2 IV SUPPLIES, Medline kit SKU ACC010271B; 2) DRAWER 2 IV FLUIDS & TUBING, Medline kit SKU ACC010416B; 3) OXYGENATION & TUBING TRAY, Medline kit SKU ACC010525C; 4)
    Category
    Medical Device
    Distribution
    Distributed nationwide