The Recall Desk

State

New Mexico product recalls

20,364 recalls have nationwide distribution and so reach New Mexico. 0 additional recalls listed New Mexico specifically in their distribution scope.

About recalls in New Mexico

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect New Mexico consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

14101–14125 of 20364

  • HighFDA (Devices)·Z-1165-2023·2023-03-01

    Diagnostic imaging system recalled for collision risk from default settings

    Siemens Luminos Agile Max diagnostic imaging systems recalled due to default configuration parameters allowing collision with room structures, risking serious injury to staff or patients.

    Product
    Luminos Agile Max with software VE10 & VF11- A diagnostic imaging system for radiographic and fluoroscopic studies Model Number: 10762472
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0343-2023·2023-03-01

    TIROSINT levothyroxine sodium oral solution recalled for subpotency nationwide

    IBSA Pharma Inc. is recalling TIROSINT (levothyroxine sodium) oral solution due to subpotency—some doses contain insufficient active ingredient. Patients should contact their pharmacist or doctor to verify their medication.

    Product
    TIROSINT — TIROSINT (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1160-2023·2023-03-01

    Respiratory care breathing circuits recalled for incorrect expiration date labeling

    S & MOHR AMERICA recalled approximately 1,320 abm Respiratory Care Standard Breathing Circuits due to incorrect expiration dates printed on product labels. The manufacturing date was printed where the expiration date should appear.

    Product
    abm Respiratory Care Standart Breating Circuit with Face Mask - Toddler REF BC21087 abm Respiratory Care Standart Breathing Circuit with Face Mask - Child/Adult Small REF BC21088 abm Respiratory Care Standart Breathing Circuit with Face Mask - Adult Large REF BC21273 abm
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0329-2023·2023-03-01

    OTC First Aid Spray Recalled for Subpotent Active Ingredient

    Dermoplast FIRST AID spray is being recalled because testing found low levels of one of its two active ingredients. The product was distributed nationwide through internet, distributors, and retailers.

    Product
    DERMOPLAST FIRST AID — DERMOPLAST FIRST AID (BENZETHONIUM CHLORIDE AND BENZOCAINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0344-2023·2023-03-01

    TIROSINT Levothyroxine Oral Solution Recalled for Subpotency

    IBSA Pharma has recalled one lot of TIROSINT (levothyroxine sodium) oral solution nationwide due to subpotency. The product contained less active ingredient than labeled.

    Product
    TIROSINT — TIROSINT (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0333-2023·2023-03-01

    TIROSINT Levothyroxine Oral Solution Recalled for Subpotent Drug Content

    IBSA PHARMA INC is recalling TIROSINT oral solution (Lot #220855) nationwide due to insufficient potency of levothyroxine sodium. The defective lot was voluntarily recalled after manufacturer discovery.

    Product
    TIROSINT — TIROSINT (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalCPSC·23136·2023-02-23

    LumaRail Bed Assist Rails recalled for entrapment and asphyxia hazard

    Platinum Health is recalling about 53,000 LumaRail bed assist rails because users can become entrapped between the rail and mattress, risking death by asphyxiation. One death has been reported.

    Product
    LumaRail Bed Assist Rails
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23129·2023-02-23

    Mainstays Three-Wick Candles Recalled for Fire and Laceration Hazards

    Star Soap Star Candle Prayer Candle recalled about 1.2 million Mainstays Three-Wick Candles because the wicks can burn too close to the glass container, causing it to break and posing fire and laceration hazards. Consumers should stop using the candles immediately and request a refund.

    Product
    Mainstays Three-Wick Candles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23135·2023-02-23

    Aderes Bookcases Recalled Due to Tip-Over and Entrapment Hazards

    TJX is recalling about 73 Aderes bookcases that can tip over if not anchored to the wall, posing tip-over and entrapment hazards that can result in death or injuries to children. Two reports of unstable bookcases have been received with no injuries reported.

    Product
    Aderes bookcases
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23130·2023-02-23

    Two Million Cosori Air Fryers Recalled for Fire and Burn Hazards

    Atekcity Corporation is recalling about 2 million Cosori air fryers because a wire connection can overheat, posing fire and burn hazards. The firm has received 205 reports of fires, with 10 minor burn injuries and 23 reports of minor property damage.

    Product
    Cosori Air Fryers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23133·2023-02-23

    1st Stage Scuba Regulators Recalled for Drowning and Injury Risk

    XDEEP 1st stage scuba regulators (model NX700) are recalled because a defective screw on the turret connection can break, creating a risk of severe injury and drowning for divers.

    Product
    1st stage scuba regulators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23132·2023-02-23

    Zinus SmartBase Euro Slats Metal Platform Bed Frames Recalled for Collapse Hazard

    Zinus is recalling about 30,400 SmartBase Euro Slats metal platform bed frames because missing reinforcing brackets can cause the frame to collapse, creating an injury hazard. Consumers should stop using the bed frames and request a free repair kit.

    Product
    SmartBase® Euro Slats Metal Platform Bed Frames
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23134·2023-02-23

    Lancaster Table & Seating High Chairs Recalled for Fall Hazard

    Clark Associates is recalling Lancaster Table & Seating brand high chairs that can break during use, posing a fall hazard to children. Three reports of high chairs breaking have been received, though no injuries have been reported.

    Product
    Lancaster Table & Seating brand High Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·23131·2023-02-23

    SCARPA F1 Ski Boots Recalled for Fall Hazard

    SCARPA North America is recalling about 770 F1 LT and F1 GT ski boots manufactured in 2022. Screws attaching the ski/walk mechanism can loosen or fall out, causing the mechanism to malfunction and posing a fall hazard.

    Product
    F1 LT and F1 GT Ski Boots
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·23729·2023-02-23

    Harbor Freight Replacement Lower Blade Guards for 12-Inch Miter Saws

    Harbor Freight Tools is recalling replacement lower blade guards for 12-inch Chicago Electric Miter Saws because they do not sufficiently cover the saw blade and can break during use, posing an injury hazard.

    Product
    Replacement lower blade guards for 12-inch Chicago Electric Miter Saws
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·23728·2023-02-23

    Polaris Timbersled Snow Bike Conversion Kits Recalled for Crash Hazard

    Polaris is recalling about 780 Timbersled snow bike conversion kits because a QuickDrive fastener can loosen during operation, causing brake failure and crash risk. No crashes or injuries have been reported.

    Product
    Polaris Timbersled Snow Bike Conversion Kits
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0298-2023·2023-02-22

    INTRALIPID 18GM Parenteral Nutrition Recalled for Lack of Sterility Assurance

    Sentara Infusion Services is recalling 7 bags of INTRALIPID 18GM, a parenteral nutrition solution, due to lack of sterility assurance. The product was dispensed to patients nationwide.

    Product
    INTRALIPID 18GM, TPN, Rx Only, use with a Curlin pump, Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320,
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1136-2023·2023-02-22

    Siemens Biograph Vision PET Scanner Gantry Locking Mechanism Recall

    Siemens recalls Biograph Vision PET scanners worldwide for a potential defect in the gantry locking mechanism that secures the equipment during scanning and service.

    Product
    SIEMENS Biograph Vision: a) 450, b) 600, c) 600 Edge
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0275-2023·2023-02-22

    Ampicillin IV Infusion Bags Recalled for Lack of Sterility Assurance

    Sentara Home Infusion Pharmacy Services is recalling 14 bags of Ampicillin 8GM in NS 400ML due to lack of sterility assurance. The affected batches were distributed nationwide to patients.

    Product
    AMPICILLIN 8GM IN NS 400ML, antibiotic, used with Curlin pump, Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320,
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0321-2023·2023-02-22

    FDA Recalls TPN Nutrition Bags Due to Sterility Assurance Failure

    Sentara Infusion Services recalls 24 bags of TPN (Total Parenteral Nutrition) distributed nationwide due to lack of sterility assurance. The recall affects prescription intravenous nutrition products.

    Product
    TPN (a) 95GM/AA, 385/DEX, 50GM/LIP 1800ML, (b)TPN AA:100GM DEX:250GM LIP:50GM 2400ML, (c) TPN: AA 80GM ; DEX 320GM ; LIP 50GM IN 2300 ml, Rx only, use with Curlin pump, Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0306-2023·2023-02-22

    Metronidazole injectable antibiotic recalled due to sterility concerns

    Sentara Infusion Services is recalling 30 bags of Metronidazole 500mg injectable antibiotic distributed nationwide due to lack of sterility assurance. Patients using the product should contact their healthcare provider.

    Product
    METRONIDAZOLE 500MG 100ML, antibiotic, Rx Only, use with a home pump or no pump, Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0307-2023·2023-02-22

    FDA recalls Milrinone injectable medication due to lack of sterility assurance

    Sentara Infusion Services recalls 83 bags of Milrinone injectable medication nationwide due to lack of sterility assurance. Patients should contact their healthcare provider immediately.

    Product
    Milrinone (a) 104MG IN 0.45% NS 130ML,(b) 108MG IN 0.45% NS 135ML, (c) 120MG IN 0.45% NS 150ML, (d) 136MG IN 0.45% NS 170ML, (e) 144MG IN 0.45% NS 180ML, (f) 160MG IN 0.45% NS 200ML, (g) 168MG IN 0.45% NS 210ML, (h) 192MG IN 0.45% NS 240ML, (i) 44MG IN 0.45% NS 55 ML, (j) 52MG IN
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0280-2023·2023-02-22

    Cefepime injectable antibiotic bags recalled due to sterility concerns

    Sentara Infusion Services is recalling 71 bags of Cefepime injectable antibiotic due to lack of sterility assurance. Patients who received affected doses should consult their healthcare provider.

    Product
    CEFEPIME, (a) 2GM IN NS 100ML (b)8GM IN NS 400ML (c) 12GM IN NS 600ML, used with a Curlin or Home pump, Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0281-2023·2023-02-22

    Cefoxitin injectable bags recalled nationwide for sterility assurance failure

    Cefoxitin injectable antibiotic (1GM and 2GM) prepared by Sentara Infusion Services is being recalled nationwide due to lack of sterility assurance. Affected patients should contact their pharmacy immediately.

    Product
    CEFOXITIN (a) 1GM IN NS 50ML,(b) 2GM IN NS 100ML, used with a home pump. Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320,
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0304-2023·2023-02-22

    Methadone Syringes Recalled for Lack of Sterility Assurance

    Sentara Infusion Services is recalling methadone syringes due to lack of sterility assurance. The affected product was dispensed to patients nationwide.

    Product
    METHADONE (a) 2.5MG IN 5ML NS SYRINGE, (b) 4MG IN 5ML NS SYRINGE, pain, Rx Only, Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320
    Category
    Drug
    Distribution
    Distributed nationwide