The Recall Desk

State

New Mexico product recalls

73,824 recalls have nationwide distribution and so reach New Mexico. 3,638 additional recalls listed New Mexico specifically in their distribution scope.

What the numbers show

Total
3,638
Critical
745
Severe
816
Most recent
2026-11-04

Of the 3,638 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 816 (22%) are Severe.

Which agencies issued them

These figures cover only the 3,638 recalls whose distribution notice names New Mexico specifically. The 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

39626–39650 of 77462

  • HighFDA (Food)·F-1651-2018·2018-07-25

    TR Toppers Chopped Chocolate Pretzel Pieces Recalled for Peanut Contamination

    T R Toppers, Inc. is recalling Chopped Chocolate Pretzel Pieces due to potential peanut contamination. Consumers should check for Lot 10481 and stop using the product.

    Product
    TR Toppers Brand Chopped Chocolate Pretzel Pieces. Item number B160-075 GTIN 0 06 51844 10599 6, 7.5 Lbs. (3 x 2.5 Lbs. Bags), Best Kept Between 34¿F and 40¿F <50% Relative Humidity
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2439-2018·2018-07-25

    Opgen Recalls AdvanDx QuickFISH Slides Due to Diminished Performance

    Opgen Inc is recalling AdvanDx QuickFISH Slides because they may show diminished performance before their expiration date.

    Product
    AdvanDx QuickFISH Slides, a component of the QuickFish BC Fixation Kit - BC, REF QFFIXBC1-25, Catalog Number: CS012 Control slides included as a component of the QFFIXBC1-25. The slides will provide non-fluorescent, wettable surface with dimensions appropriate for testing…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2480-2018·2018-07-25

    Cardinal Health Recalls Presource PBDS Kits Due to Leaking Gatorade Pouches

    Cardinal Health is recalling 8,928 Presource PBDS kits because a defect in the Gatorade pouch seal caused the pouch to leak within the kit.

    Product
    Presource PBDS, Kit, Common Diabetes. Kit includes a exerciser volumetric 5000 ML device, two items of cloth, skin prep 2% CHG, a packet of 4 chlorhexidine gluconate antiseptic cloths, and Gatorade pouches. Product Usage: The kit is provided to a patient pre-surgery, as…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0920-2018·2018-07-25

    Hain Celestial Recalls alba BOTANICA Sunscreen Due to Incorrect Formulation

    The Hain Celestial Group is recalling alba BOTANICA sport mineral sunscreen because the wrong product formulation was placed in the packages.

    Product
    alba BOTANICA sport mineral sunscreen (titanium dioxide 7.0% and zinc oxide 9.0%), spf 45, 170 g (6 oz) tubes packaged in a) 4 tubes per case; b) 8 pack shipper display; Manufactured By: The Hain Celestial Group, Inc., Lake Success, NY 11042, UPC 7 24742 01102 4.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2496-2018·2018-07-25

    Philips Ingenuity Digital PET/CT System Recall for Pallet Assembly Defect

    Philips is recalling 32 Ingenuity Digital PET/CT Systems because a block connecting the patient pallet to the couch may be assembled incorrectly, potentially causing a misaligned screw.

    Product
    Ingenuity Digital PET/CT System, Model 882446 with the following UDI's: (01)00884838059559(21)900004 (01)00884838059559(21)900005 (01)00884838059559(21)900006 (01)00884838059559(21)900007 (01)00884838059559(21)900008 (01)00884838059559(21)900009…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2482-2018·2018-07-25

    Cardinal Health Recalls Presource PBDS Kits Due to Leaking Gatorade Pouches

    Cardinal Health is recalling Presource PBDS kits because a defect in the Gatorade pouch seal caused the pouch to leak within the kit.

    Product
    Presource PBDS, Kit, No Spiro. Kit includes a exerciser volumetric 5000 ML device, two items of cloth, skin prep 2% CHG, a packet of 4 chlorhexidine gluconate antiseptic cloths, and Gatorade pouches. Product Usage: The kit is provided to a patient pre-surgery, as part of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2484-2018·2018-07-25

    Stryker Recalls Reprocessed Harmonic Ace Shears Due to Error Code

    Stryker is recalling 180 reprocessed Harmonic Ace shears because they may display an error code preventing use.

    Product
    Reprocessed HARMONIC Ace¿ +7, 5mm Diameter Shears with Advanced Hemostasis (HARH), Item Number HARH36 Product Usage: The Reprocessed HARMONIC ACE¿+7, 5 mm Diameter Shears with Advanced Hemostasis are indicated for soft tissue incisions when bleeding control and minimal…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2436-2018·2018-07-25

    Siemens Dimension Vista CTNI Sample Diluent Recalled for Defective Cap Septum

    Siemens Healthcare Diagnostics is recalling 1,446 units of Dimension Vista CTNI Sample Diluent because a defective cap septum may cause erroneously elevated test results.

    Product
    Dimension Vista¿ CTNI Sample Diluent, KD692, SMN# 10445205
    Category
    Medical Device
    Distribution
    53 states
  • ModerateFDA (Devices)·Z-2430-2018·2018-07-25

    Valeris Medical Recalls Apollo XT Suture Anchors Due to Material Mislabeling

    Valeris Medical is recalling 113 Apollo XT Suture Anchors because the labels incorrectly identified the material as titanium instead of PEEK.

    Product
    Apollo XT Suture Anchor, 5.5 x 15 Product Usage: Apollo XT Suture Anchors are intended for: Shoulder - Rotator Cuff Repair - Bankart Repair - SLAP Lesion Repair - Biceps Tenodesis - Acromio-Clavicular Separation Repair - Deltoid Repair - Capisular Shift or Capsulolabral…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2468-2018·2018-07-25

    Fx Solutions Proton Beam Therapy Heads Recalled for Blister Breach

    Fx Solutions is recalling specific proton beam therapy heads due to a breach in the external blister packaging.

    Product
    Fx SOLUTIONS CENTERED HEAD CoCr 50x19, REF 106-5019 Product Usage: Device is designed to produce and deliver proton beam for the treatment of patients with localized tumors and other conditions susceptible to treatment by radiation. The PTS may include a fixed small beam…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2483-2018·2018-07-25

    Cardinal Health Recalls Presource PBDS Kits Due to Leaking Gatorade Pouches

    Cardinal Health is recalling 8,928 Presource PBDS kits because a defect in the Gatorade pouch seal caused the pouch to leak within the kit.

    Product
    Presource PBDS, Kit, No Spiro Diabetes. Kit includes a exerciser volumetric 5000 ML device, two items of cloth, skin prep 2% CHG, a packet of 4 chlorhexidine gluconate antiseptic cloths, and Gatorade pouches. Product Usage: The kit is provided to a patient pre-surgery, as…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2469-2018·2018-07-25

    Fx Solutions Offset Heads Recalled for Blister Breach

    Fx Solutions is recalling specific lots of Humelock Offset Heads due to a breach in the external blister packaging.

    Product
    Fx SOLUTIONS OFFSET HEAD CoCr 50x20, REF 106-5000 Product Usage: Device is designed to produce and deliver proton beam for the treatment of patients with localized tumors and other conditions susceptible to treatment by radiation. The PTS may include a fixed small beam…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2442-2018·2018-07-25

    Health Harmony Mobile App Recalled for Data Synchronization Delays

    Intel-GE Care Innovations LLC is recalling the Health Harmony Mobile application because patient data sometimes failed to sync with the backend database in a timely manner.

    Product
    Health Harmony Mobile application software Product Usage: Care Innovations Health Harmony Mobile is intended as a communication tool to display medical device data from third party devices for patients to view, and to collect assessment (question &#38; answers) from…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2438-2018·2018-07-25

    Siemens Dimension Vista MULTI 2 SDIL Diluent Recall for Defective Septum

    Siemens is recalling 1,195 units of Dimension Vista MULTI 2 SDIL diluent because a defective septum may cause erroneously elevated test results.

    Product
    Dimension Vista¿ MULTI 2 SDIL, KD694, SMN# 10483586
    Category
    Medical Device
    Distribution
    53 states
  • ModerateFDA (Devices)·Z-2481-2018·2018-07-25

    Cardinal Health Recalls Presource PBDS Kits Due to Gatorade Pouch Seal Defect

    Cardinal Health is recalling 8,928 Presource PBDS kits because a defect in the Gatorade pouch seal caused the pouch to leak within the kit.

    Product
    Presource PBDS, Kit, Common. Kit includes a exerciser volumetric 5000 ML device, two items of cloth, skin prep 2% CHG, a packet of 4 chlorhexidine gluconate antiseptic cloths, and Gatorade pouches. Product Usage: The kit is provided to a patient pre-surgery, as part of the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E060000·2018-07-24

    SynTec Recalls School Bus Seats Due to Mounting Foot Defect

    SynTec is recalling S3B 45-inch Restraint School Bus Seats because the mounting foot may pull through the bolted joint at the bus floor, increasing injury risk in a crash.

    Product
    SEATS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18192·2018-07-24

    JCPenney Recalls Okie Dokie Shorts Due to Choking Hazard

    JCPenney is recalling Okie Dokie Denim Patches Shortie shorts because the patches can detach, posing a choking hazard to young children.

    Product
    Okie Dokie Denim Patches Shortie shorts
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·18190·2018-07-24

    Ross Stores Recalls Bistro Chairs Due to Frame Breakage and Fall Hazard

    Ross Stores is recalling Bronze Hammered bistro chairs because the frames can break, posing a fall hazard. Consumers should stop using the chairs and return them for a full refund.

    Product
    Bistro chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18V488000·2018-07-23

    Karma Revero Recalled for Non-Compliant Driver Side Rearview Mirror Glass

    Karma Automotive is recalling 2018 Revero vehicles because the driver's side exterior rearview mirror may use convex glass instead of flat glass, failing federal safety standards.

    Product
    KARMA — KARMA REVERO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E058000·2018-07-20

    Meritor Recalls Wheel Studs Due to Potential Heat Treatment Defect

    Meritor is recalling specific wheel studs installed in steer axle hubs because improper heat treatment may cause them to fail, potentially leading to wheel detachment.

    Product
    WHEELS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E059000·2018-07-20

    Jost Recalls Fifth Wheel Assemblies Due to Narrow Bracket Risk

    Jost International is recalling certain Outboard Sliders because a narrow bracket may allow the trailer to separate from the tractor, increasing crash risk.

    Product
    TRAILER HITCHES:FIFTH WHEEL ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V489000·2018-07-20

    BraunAbility Recalls Wheelchair Vans Due to Brake Line Connection Defect

    Braun Corporation is recalling 2012-2018 BraunAbility Dodge and Chrysler wheelchair vans because brake lines may be disconnected, reducing electronic stability control performance.

    Product
    BRAUNABILITY — BRAUNABILITY DODGE WHEELCHAIR VAN, CHRYSLER WHEELCHAIR VAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V487000·2018-07-20

    Freightliner Recalls M2 Trucks for Steering Shaft Installation Defect

    Daimler Trucks is recalling 2018-2019 Freightliner Business Class M2 trucks because an incorrectly installed steering shaft may disconnect the steering wheel from the front wheels.

    Product
    FREIGHTLINER — FREIGHTLINER BUSINESS CLASS M2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V472000·2018-07-20

    Van-Con Recalls School Buses Due to Seat Foam Crash Protection Defect

    Van-Con is recalling 2011-2018 33803 Dual Rear Wheel school buses because seat foam may not absorb enough impact in a crash, increasing injury risk.

    Product
    VAN-CON — VAN-CON 33803 DUAL REAR-WHEEL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·pha-07202018-1·2018-07-20

    FSIS Public Health Alert for Hungry Man Dinners with Recalled Whey Powder

    The USDA FSIS issued a public health alert for Hungry Man frozen dinners containing whey powder recalled due to possible Salmonella contamination. No adverse reactions have been reported.

    Product
    FSIS Issues Public Health Alert For Products Containing FDA-Regulated Whey Powder That Has Been Recalled Due To Possible Salmonella Contamination
    Category
    Food
    Distribution
    Distributed nationwide