The Recall Desk

State

New Mexico product recalls

73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

31976–32000 of 77374

  • ModerateFDA (Devices)·Z-0711-2020·2019-12-25

    Angiodynamics Recalls MICRO-PSD Electron Sensors Due to Accuracy Concerns

    Angiodynamics, Inc. is recalling 36 units of MICRO-PSD Electron sensors because they may provide readings outside the expected accuracy range.

    Product
    MICRO-PSD Electron, Catalog Number: PSD-EE5N - Product Usage: pre-calibrated PSD sensors are intended for use during cancer treatments to measure photon and electron radiation therapy as an adjunct to treatment planning permitting measurement and validation of radiation dose…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0703-2020·2019-12-25

    Teleflex Sheridan Endobronchial Tubes Recalled for Incorrect Labeling

    Teleflex Medical is recalling Sheridan Endobronchial Tubes due to incorrectly labeled tracheal and bronchial swivel connectors.

    Product
    HUDSON RCI SHERIDAN SHERI-BRONCH Endobronchial Tube REF 5-16135 - Product Usage: The Sheridan Endobronchial Tubes are intended for use in Thoracic surgery, brochospirometry, adminitration of endobronchial anesthesia and other uses commonly requiring endobronchial intubation. The…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0691-2020·2019-12-25

    Integra Recalls Mislabeled Ascension Silicone PIP Joint Implants

    Integra Lifesciences is recalling nine Ascension Silicone PIP implants that were mislabeled as size 1 but contained size 0 implants.

    Product
    Ascension¿ Silicone PIP-Silicone PIP Sz 1, Model Number: SPIP5201WW - Product Usage: The Ascension Silicone PIP implant is intended for cementless replacement of the proximal interphalangeal joint in patients with advanced osteoarthritis, post-traumatic arthritis and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0713-2020·2019-12-25

    Angiodynamics Recalls Micro-PSD External Beam Photon Sensors

    Angiodynamics, Inc. is recalling 48 Micro-PSD External Beam Photon sensors due to potential accuracy issues. The devices are used to measure radiation therapy during cancer treatment.

    Product
    MICRO-PSD EXTERNAL BEAM PHOTON, Catalog Number: PSD-PE5N - Product Usage: pre-calibrated PSD sensors are intended for use during cancer treatments to measure photon and electron radiation therapy as an adjunct to treatment planning permitting measurement and validation of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0708-2020·2019-12-25

    Rhondium OVC3 One Visit Crown Recalled for Incorrect Expiration Date

    Rhondium Limited is recalling six OVC3 One Visit Crown devices because they were mislabeled with an incorrect expiration date.

    Product
    Rhondium OVC3 One Visit Crown, Model FDI 24/25L USA 12/13L A2 HT, Nonsterile, Rx. The firm name on the label is Rhondium Ltd., Katikati, New Zealand.
    Category
    Medical Device
    Distribution
    4 states
  • LowFDA (Devices)·Z-0717-2020·2019-12-25

    Boston Scientific Recalls AngioJet Ultra Consoles Missing Operator's Manuals

    Boston Scientific is recalling 169 AngioJet Ultra Consoles because they were shipped without the required Operator's Manual.

    Product
    AngioJet Ultra Consoles-Thrombectomy System UPN: 105650-001D 105650-001H 105650-001R 105650-001Z 105650-002R 105650-004H 105650-004R 105650-007R 105650-009R 105650-024H 105650-024Z 105650-025 105650-025H 105650-025R 105650-026R Product Usage - The AngioJet…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0623-2020·2019-12-25

    Apothecus Recalls VCF Vaginal Contraceptive Foam Due to Canister Leakage

    Apothecus Pharmaceutical Corp. is recalling VCF Vaginal Contraceptive Foam cans and case packs because the canister units exhibit propellant leakage, rendering the product unusable.

    Product
    VCF Vaginal Contraceptive Foam, a) can, 13 applications per can, Net wt. 0.6 oz (17g). NDC 52925-312-14, b) case pack with 36 cans in a nested container. Net wt 0.6 oz (17g) per can. NDC 52925-312-06, Distributed By: Apothecus Pharmaceutical Corp. Oyster Bay, NY 11771.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0699-2020·2019-12-25

    Allergan Natrelle Breast Implant Recall for Unreadable 2D Barcodes

    Allergan is recalling Natrelle saline-filled breast implants because 2D barcodes may be unreadable by GS-1 scanners due to formatting errors.

    Product
    Natrelle Saline-Filled Breast Implant, for the following Styles and sizes, Style LP, Style 68 HP, Style 68 MP, Style LP/UDI: NATRELLE Style 68LP-125 Saline Round Low 10888628000513, NATRELLE Style 68LP-150 Saline Round Low 10888628000520, NATRELLE Style 68LP-175 Saline…
    Category
    Medical Device
    Distribution
    47 states
  • LowFDA (Devices)·Z-0700-2020·2019-12-25

    Allergan Recalls Natrelle Breast Implants Due to Unreadable 2D Barcodes

    Allergan is recalling Natrelle silicone breast implants because 2D barcodes may be unreadable by GS-1 scanners due to non-standard formatting.

    Product
    Natrelle Silicone Filled Breast Implants for the following Styles and Sizes: Style 10, Style 15, Style 20, Style 40, Style 45 Style 10/UDI: NATRELLE Style 10-180 Gel Round Mod 10888628001206, NATRELLE Style 10-210 Gel Round Mod 10888628001213, NATRELLE Style 10-240 Gel…
    Category
    Medical Device
    Distribution
    47 states
  • LowFDA (Devices)·Z-0702-2020·2019-12-25

    Allergan Recalls Breast Implant Sizers Due to Unreadable Barcodes

    Allergan is recalling NATRELLE Resterilizable Sizers because 2D barcodes may be unreadable by GS-1 scanners due to non-standard formatting.

    Product
    NATRELLE Resterilizable Sizers for the styles and sizes: Style 15, Style 20, Inspira X (responsive gel), Inspira F (responsive gel), Inspira LP (responsive gel), Inspira M (responsive gel), Inspira L (responsive gel), Inspira ST L (Soft Touch gel), Inspira ST LP (Soft Touch…
    Category
    Medical Device
    Distribution
    47 states
  • LowFDA (Devices)·Z-0701-2020·2019-12-25

    Allergan Recalls Breast Implants With Non-Standard 2D Barcodes

    Allergan is recalling Natrelle Inspira silicone-filled breast implants because 2D barcodes may be unreadable by GS-1 scanners due to formatting errors.

    Product
    Natrelle Inspira Sillicone-Filled Breast Implants for the following Styles and Sizes: 7607 SSM, 7608 SSF, 7609 SSX, 7513 SRL, 7514 SRLP, 7515 SRM, 7516 SRF, 7517 SRX, 7626 SCL, 7627 SCLP, 7628 SCM, 7629 SCF, 7630 SCX: 7607 SSM/UDI: Natrelle Inspira SSM 140cc BI (US)…
    Category
    Medical Device
    Distribution
    47 states
  • SevereNHTSA·19V916000·2019-12-23

    Daimler Trucks Recalls 2020 FCC MT45G Vehicles Due to Fire Risk

    Daimler Trucks North America is recalling 2020 FCC MT45G vehicles because a battery support module can short circuit, increasing the risk of a fire.

    Product
    FCCC — FCCC MT45G
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V917000·2019-12-20

    Peterbilt Recalls 2018-2019 520 Trucks for Steering Bracket Defect

    PACCAR is recalling 2018-2019 Peterbilt 520 trucks because a steering assist bracket may be improperly mounted, risking steering lockup and crashes.

    Product
    PETERBILT — PETERBILT 520
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V918000·2019-12-20

    Mercedes-Benz Recalls Vehicles for Sunroof Glass Detachment Risk

    Mercedes-Benz is recalling 747,928 vehicles from 2001-2011 because the sunroof glass panel may detach, creating a road hazard.

    Product
    MERCEDES BENZ — MERCEDES BENZ, MERCEDES-BENZ CLK320, C230, CLK550, E320
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V912000·2019-12-20

    BMW Recalls 2019-2020 330i Models Due to Rear Seat Belt Defect

    BMW is recalling 2019-2020 330i and 330i xDrive vehicles because the outboard rear seat belt pretensioners may not lock during a crash, increasing injury risk.

    Product
    BMW — BMW 330I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20046·2019-12-20

    Bosch Recalls Buderus GB125-35 Boilers Due to Carbon Monoxide Hazard

    Bosch Thermotechnology is recalling Buderus GB125-35 oil-condensing boilers because a blocked siphon can cause delayed ignition and carbon monoxide release. No injuries have been reported in the U.S.

    Product
    Buderus GB125-35 oil-condensing boilers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateNHTSA·19V914000·2019-12-20

    Mercedes-Benz Recalls 2019 GLC Models for Incorrect Air Bag Labels

    Mercedes-Benz is recalling 2019 GLC models because passenger-side sun visors may have air bag warning labels in a foreign language, potentially obscuring safety risks.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG GLC63S, AMG GLC43, GLC 300, GLC350E
    Category
    Vehicle
    Distribution
    Distributed nationwide