The Recall Desk

State

New Mexico product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

36751–36775 of 77447

  • ModerateFDA (Food)·F-1097-2019·2019-03-06

    Planetary Herbals Mullein Lung Complex Recalled for Labeling Error

    Planetary Herbals is recalling Mullein Lung Complex capsules due to a labeling error regarding inactive ingredients.

    Product
    Planetary Herbals Mullein Lung Complex; 1000 mg; 15 count, item number PF0003; 90 count - Item number PF0002; 180 count, Item number PF0106 and 90 + 90 count, PF 7013 white plastic bottles. Proprietary Blend: Platycodon root, Ophiopagon Rhizome, Long Pepper Fruit, Black…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1054-2019·2019-03-06

    King Orchards Tart Cherry Concentrate Recalled for Incorrect Sugar Labeling

    King Orchards is recalling Montmorency Tart Cherry Concentrate because the nutrition label lists 1g of sugar per serving instead of the actual 15g.

    Product
    Montmorency Tart Cherry Concentrate 100% Juice 32-oz bottle (sold individual and 12 per case), 16-oz bottle (sold individual and 12 per case), and 1-oz packet (sold individual and per 25, 50, 100, 250, 300, and 1000)
    Category
    Food
    Distribution
    20 states
  • ModerateFDA (Devices)·Z-0933-2019·2019-03-06

    Becton Dickinson Recalls Phoenix AST-s Indicator Due to Test Aborts

    Becton Dickinson is recalling Phoenix AST-s Indicator lots because they cause increased test aborts. The products were distributed to 41 US states and 33 foreign countries.

    Product
    Phoenix AST-s Indicator, Catalog Number 246009
    Category
    Medical Device
    Distribution
    42 states
  • ModerateFDA (Devices)·Z-0967-2019·2019-03-06

    Cook Inc. Recalls Gastrointestinal Suture Anchor Sets Due to Retention Mechanism Issue

    Cook Inc. is recalling 797 Entuit Secure Gastrointestinal Suture Anchor Sets because a specific extension spring lot may cause difficulty sliding the retention mechanism.

    Product
    Entuit Secure Gastrointestinal Suture Anchor Set, Catalog Number GIAS-SRM-2, Order Number G35569 The Entuit Secure Gastrointestinal Suture Anchor Set is intended for anchoring the anterior wall of the stomach to the abdominal wall prior to the introduction of interventional…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0959-2019·2019-03-06

    Shimadzu BRANSIST safire Digital Angiography System Software Recall

    Shimadzu Medical Systems is recalling eight BRANSIST safire digital angiography systems due to a software error that can cause abnormal termination during initial patient registration.

    Product
    BRANSIST safire Product Usage: DIGITAL ANGIOGRAPHY SYSTEM This system is intended to be used for radiologic visualization of the heart, blood vessels or lymphatic system during or after injection of a contrast medium. It is to be used in the diagnosis of the circulatory…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0968-2019·2019-03-06

    Cook Inc. Recalls Gastrointestinal Suture Anchor Sets Due to Retention Mechanism Issue

    Cook Inc. is recalling 975 Entuit Secure Gastrointestinal Suture Anchor Sets because a specific extension spring lot may cause difficulty sliding down the retention mechanism.

    Product
    Entuit Secure Gastrointestinal Suture Anchor Set, Catalog Number GIAS-SRM-3, Order Number G35570 The Entuit Secure Gastrointestinal Suture Anchor Set is intended for anchoring the anterior wall of the stomach to the abdominal wall prior to the introduction of interventional…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0935-2019·2019-03-06

    Becton Dickinson Recalls Phoenix AP AST Indicator Bags Due to Test Aborts

    Becton Dickinson is recalling Phoenix AP AST Indicator Bags because certain lots cause increased test aborts. The products were distributed to 40 US states and 33 foreign countries.

    Product
    Phoenix AP AST Indicator Bag, Catalog Number 246006
    Category
    Medical Device
    Distribution
    42 states
  • ModerateFDA (Devices)·Z-0960-2019·2019-03-06

    Abbott Vascular Recalls PLUS 30 Priority Pack Accessory Kit Due to Expiration Error

    Abbott Vascular is recalling 26 units of the PLUS 30 Priority Pack Accessory Kit because an incorrect expiration date was entered for one lot.

    Product
    PLUS 30 PRIORITY PACK Accessory Kit Product Usage: Is recommended for use during vascular procedures in conjunction with interventional and / or diagnostic devices (e.g., balloon dilatation catheters, atherectomy devices, stent delivery systems, intravascular ultrasound…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0934-2019·2019-03-06

    Becton Dickinson Recalls Phoenix AST Indicator Due to Test Aborts

    Becton Dickinson is recalling Phoenix AST Indicator lots because panels show increased test aborts. The recall covers 62,880 units distributed in the US and 33 foreign countries.

    Product
    Phoenix AST Indicator, Catalog Number 246004
    Category
    Medical Device
    Distribution
    42 states
  • LowFDA (Drugs)·D-0517-2019·2019-03-06

    Lupin Recalls Moxifloxacin Ophthalmic Solution Due to Impurity Levels

    Lupin Pharmaceuticals is recalling Moxifloxacin Ophthalmic Solution because impurity levels exceeded specifications. The recall covers 674,628 bottles distributed nationwide and in Puerto Rico.

    Product
    MOXIFLOXACIN — MOXIFLOXACIN (MOXIFLOXACIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0958-2019·2019-03-06

    Exactech Equinoxe Humeral Stem Recalled for Incorrect Packaging Instructions

    Exactech is recalling 40 Equinoxe Preserve Humeral Stems because they may have been packaged with instructions for a different knee implant.

    Product
    Equinoxe Preserve Humeral Stem, 8mm Product Usage: The Equinoxe Preserve Stems are indicated for use in skeletally mature individuals with degenerative diseases of the glenohumeral joint where anatomic total arthroplasty,anatomic hemi-arthroplasty,or reverse total…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V169000·2019-03-05

    Jayco Recalls 2017-2019 Seismic Fifth Wheel Trailers for Brake Line Defect

    Jayco is recalling 2017-2019 Seismic fifth wheel trailers with optional hydraulic brakes because brake lines may be pinched or cut, increasing crash risk.

    Product
    JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL, JAYCO SEISMIC, redundant SEISMIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V173000·2019-03-05

    Jayco Recalls 2019 Fifth Wheel Trailers Due to Awning Fuse Error

    Jayco is recalling 2019 North Point and Pinnacle fifth wheel trailers because an incorrect fuse in the awning circuit increases the risk of fire.

    Product
    JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL PINNACLE, NORTH POINT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V175000·2019-03-05

    Entegra Esteem Motorhomes Recalled for Parking Brake Cable Defect

    Entegra is recalling 2019 Esteem motorhomes because parking brake cable ends may be too small, allowing the cable to disconnect and preventing the emergency brake from engaging.

    Product
    ENTEGRA — ENTEGRA ESTEEM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V176000·2019-03-05

    Kenworth Trucks Recalled for Potential Rear Axle Oil Deficiency

    PACCAR is recalling 2020 Kenworth T680, T800, T880, W900, and W990 trucks because rear axles may lack oil, increasing crash risk.

    Product
    KENWORTH — KENWORTH T680, T800, T880, W900
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V171000·2019-03-05

    2019 Western Star Trucks Recalled for Odometer Unit Labeling Error

    Daimler Trucks North America is recalling 2019 Western Star 4700 and 4900 trucks because the odometer displays miles but tracks kilometers, potentially causing driver confusion.

    Product
    WESTERN STAR — WESTERN STAR 4700, 4900
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V170000·2019-03-05

    Thomas Built Buses Minotour Recalled for Wheelchair Lift Safety Defect

    Daimler Trucks North America is recalling 2003-2019 Thomas Built Buses Minotour school buses because the wheelchair lift can operate without the parking brake engaged, posing an injury risk.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES MINOTOUR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V162000·2019-03-04

    Darley Recalls 2017-2019 Fire Trucks Due to Brake Light Wiring Defect

    W. S. Darley & Co. is recalling 2017-2019 WASP fire trucks because brake lights may illuminate without the pedal being pressed, potentially confusing other drivers.

    Product
    DARLEY — DARLEY FIRE APPARATUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V163000·2019-03-04

    LDV Command Center and Emergency Response Vehicles Recalled for Brake Light Defect

    LDV, Inc. is recalling 2017-2018 Command Center and Emergency Response vehicles because brake lights may illuminate without the pedal being pressed, potentially confusing other drivers.

    Product
    LDV, INC. — LDV, INC. COMMAND CENTER, EMERGENCY RESPONSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V165000·2019-03-04

    KZRV Recalls 2019 RVs Due to Cooktop Flame Inversion Risk

    KZRV is recalling 2019 Sportsmen, Escape, and Sonic Lite trailers because the cooktop flame may invert, increasing burn risk.

    Product
    KZRV — KZRV SPORTSMEN, ESCAPE, SONIC LITE
    Category
    Vehicle
    Distribution
    Distributed nationwide