The Recall Desk

State

Colorado product recalls

20,199 recalls have nationwide distribution and so reach Colorado. 0 additional recalls listed Colorado specifically in their distribution scope.

About recalls in Colorado

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 Colorado 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.

10026–10050 of 20199

  • HighFDA (Devices)·Z-1219-2024·2024-03-06

    Hip Implant Component Mislabeled With Wrong Insert Type on Packaging

    LINK BiMobile hip implant liners are being recalled because packaging incorrectly identifies the insert type as F instead of G. This labeling error could delay surgery or result in the wrong component being used.

    Product
    LINK BiMobile Dual Mobility System E-Poly Liner for 28mm Head, 70mm Shell- Indicated for patients with mobility-limiting diseases, fractures or defects of the hip joint or proximal femur. Item Number: 184-280/12
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V458000·2024-03-06

    2020-2022 Hyundai Venue seat belt pretensioners may explode in crash

    Hyundai is recalling 2020-2022 Venue vehicles because the front seat belt pretensioners may explode when deployed in a crash, potentially projecting metal fragments at occupants.

    Product
    HYUNDAI — 2021 HYUNDAI VENUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1098-2024·2024-03-06

    MEDLINE Medical Device Kits Recalled for Potential Sterility Issues

    Medline Industries recalls multiple medical device kits and trays manufactured with components that may lack sterility. The affected solutions could be non-sterile, posing a potential safety risk.

    Product
    MEDLINE Kits, trays, and packs labeled as follows: a) Description, REF DYNDH1679; b) BREAST BIOPSY TRAY, REF DYNDH1664; c) BREAST BIOPSY TRAY, REF DYNDH1431A; d) BREAST BIOPSY TRAY, REF DYNJ46448; e) BREAST BIOPSY TRAY, REF DYKE1520B; f) COLON KIT- BERLIN, REF DYNDH1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1198-2024·2024-03-06

    Integra Cranial Access Kit recalls due to packaging sterility defect

    Integra LifeSciences is recalling 161 units of the Cranial Access Kit (Lot 7124720) due to packaging defects that may compromise sterility. The recall affects units distributed worldwide.

    Product
    Ref No: INS7260 / Integra¿ Cranial Access Kit. For access to the subarachnoid space or the lateral ventricles of the brain.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0354-2024·2024-03-06

    FDA recalls Lubricant PM Ointment due to sterility assurance failure

    Lubricant PM Ointment is being recalled by AACE Pharmaceuticals due to the manufacturer's failure to assure the product was manufactured under sterile conditions.

    Product
    Lubricant PM Ointment (Mineral Oil 42.5% and White Petrolatum 57.3%), Packaged in 3.5 gram tubes, Distributed by: AACE Pharmaceuticals, Inc., Fairfield, NJ 07004, NDC 71406-124-35, UPC 371406124356
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1205-2024·2024-03-06

    Colonoscope Model CF-H180AL Recalled Due to Missing Protective Adhesive

    Olympus is recalling 36 colonoscopes with specific serial numbers that lack a protective adhesive, risking device failure if exposed to vibration, temperature changes, or shock loads.

    Product
    Colonoscope, Model Number CF-H180AL.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0350-2024·2024-03-06

    Mesalamine extended-release capsules recalled due to dissolution failure

    Sun Pharmaceutical is recalling Mesalamine extended-release capsules due to failed dissolution specifications. The affected capsules may not dissolve and release medication properly.

    Product
    MESALAMINE — MESALAMINE (MESALAMINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1211-2024·2024-03-06

    Colonoscope Model PCF-H190L Recalled for Missing Protective Adhesive

    Olympus Corporation recalled 31 colonoscopes lacking a protective adhesive that shields against vibration, temperature fluctuations, and shock. The missing adhesive may affect device structural integrity under physical stress.

    Product
    Colonoscope, Model Number PCF-H190L.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0363-2024·2024-03-06

    Lidocaine and Phenylephrine Injectable Vials Recalled for Glass Delamination

    Denver Solutions is recalling Lidocaine-Phenylephrine injectable vials nationwide due to glass delamination in the vials. The defect could potentially introduce glass fragments into the medication.

    Product
    Lidocaine HCL 1% (10mg/mL), PHENYLephrine HCL 1.5% (15mg/mL), 1 ml in a Single- Dose Vial, RX Only, Leiters 13796 Compark Blvd, Englewood, CO 80112, NDC 71449-090-42
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1207-2024·2024-03-06

    Colonoscope Model CF-HQ190L Recalled Due to Missing Protective Adhesive

    Olympus Corporation is recalling 97 Colonoscope Model CF-HQ190L units distributed nationwide. The devices were assembled without protective adhesive, risking malfunction under vibration, temperature changes, or shock.

    Product
    Colonoscope, Model Number CF-HQ190L.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1201-2024·2024-03-06

    Integra Cranial Access Kit Recalled for Compromised Sterile Packaging

    Integra LifeSciences is recalling 8,906 units of the Cranial Access Kit because the sterile packaging failed integrity testing, potentially compromising sterility. Units were distributed worldwide.

    Product
    Ref No: INSHITH / Integra¿ Cranial Access Kit. For access to the subarachnoid space or the lateral ventricles of the brain.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23V431000·2024-03-06

    Honda Odyssey, Pilot, Passport Rearview Camera Display Failure Recall

    A faulty MOST cable connector in certain 2018-2023 Honda Odyssey, Pilot, and Passport vehicles may prevent the rearview camera image from displaying, reducing rear visibility and increasing crash risk.

    Product
    HONDA — 2022 HONDA PASSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1001-2024·2024-03-06

    Reser's Amish Macaroni Salad recalled for undeclared wheat allergen

    Reser's Amish Macaroni Salad is recalled because some containers have a mislabeled side label that does not declare wheat, which is an ingredient in the product. This poses a risk to people with wheat allergies.

    Product
    The recalled Reser's Amish Macaroni Salad was packaged in a plastic clear container where the top lid is labeled as Reser's Amish Macaroni Salad, Net Wt. 1lb., and the container side label indicates Reser s Southern Style with Egg Potato Salad, Net Wt. 1lb. UPC 0 71117 19044 1.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0349-2024·2024-03-06

    FDA Recalls Fluticasone Propionate Nasal Spray Due to Suspected Bacterial Contamination

    The FDA is recalling Fluticasone Propionate Nasal Spray due to suspected potential presence of Burkholderia cepacia complex bacteria. The affected lot (TX5275) was distributed nationwide.

    Product
    FLUTICASONE PROPIONATE — FLUTICASONE PROPIONATE (FLUTICASONE PROPIONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1199-2024·2024-03-06

    Integra Cranial Access Kit recall over sterile packaging defect

    Integra LifeSciences is recalling the Cranial Access Kit due to a defect in the sterile packaging that may compromise product sterility. Affects 30 units distributed worldwide.

    Product
    Ref No: INS7270 / Integra¿ Cranial Access Kit. For access to the subarachnoid space or the lateral ventricles of the brain.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1183-2024·2024-03-06

    Infusion Pumps Model Z-800WF Recalled Due to Alarm Volume Malfunction

    Zyno Medical recalls Z800 infusion pumps (Model Z-800WF) with software version 5.2.05 due to a potential alarm volume malfunction. The alarm may revert to low volume, delaying therapy and risking organ failure in extreme cases.

    Product
    Zyno Medical Z800 Large Volume Infusion Pumps -Intended to provide intravenous infusion of parenteral fluids, blood and blood products to a patient under the direction or supervision of physician or other certified health care professional Model: Z-800WF
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0359-2024·2024-03-06

    7 Eleven Hand Sanitizer Gel recalled for manufacturing facility deficiencies

    Seatex LLC is recalling 1,282 cases of 7 Eleven Hand Sanitizer Gel due to manufacturing facility deficiencies found during FDA inspection. The product was distributed nationwide.

    Product
    7 Eleven Hand Sanitizer Gel, Ethanol 70% v/v Antiseptic, Mountain Spring Scent, 1250 mL cases, Magnus 16005 Gateway Drive, Ste 300, Frisco, TX 75033
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1213-2024·2024-03-06

    Colonoscope Model PCF-HQ190L Recalled for Missing Protective Adhesive

    Olympus is recalling 28 colonoscopes (Model PCF-HQ190L) due to missing adhesive that protects the device from vibration, temperature changes, and physical shock. The defect could cause device malfunction during procedures.

    Product
    Colonoscope, Model Number PCF-HQ190L.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·24V388000·2024-03-06

    2024 Forest River travel trailers recalled for insufficient tire clearance

    Forest River is recalling 2024 Rainier, Stealth Evo, Salem, Vibe, and Wildwood travel trailers due to insufficient tire clearance that may cause tire damage and loss of vehicle control.

    Product
    FOREST RIVER — 2024 FOREST RIVER RAINIER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V428000·2024-03-06

    2023 Grand Design Momentum Toy Hauler Recall: Incorrect Cargo Capacity Label

    Grand Design RV is recalling certain 2023 Momentum toy haulers due to an incorrect Cargo Carrying Capacity label. The mislabeled weight information can lead to vehicle overload, increasing crash risk.

    Product
    GRAND DESIGN — 2023 GRAND DESIGN MOMENTUM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1212-2024·2024-03-06

    Olympus colonoscope PCF-H190TL recalled for missing protective adhesive

    Olympus has recalled certain repaired colonoscope models lacking protective adhesive that could fail under vibration, temperature, or severe shock loads. Affected models include the PCF-H190TL, distributed nationwide.

    Product
    Colonoscope, Model Number PCF-H190TL.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1206-2024·2024-03-06

    Colonoscope Model CF-HQ190I recalled for missing protective adhesive

    Olympus is recalling certain repaired Model CF-HQ190I colonoscopes assembled without protective adhesive, which may cause equipment failure under vibration, temperature changes, or shock.

    Product
    Colonoscope, Model Number CF-HQ190I.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1197-2024·2024-03-06

    Integra Cranial Access Kit Recalled Due to Packaging Integrity Defect

    Integra LifeSciences is recalling 188 units of the Integra Cranial Access Kit because defective sterile packaging may have compromised product sterility.

    Product
    Ref No: INS7250 / Integra Cranial Access Kit. For access to the subarachnoid space or the lateral ventricles of the brain.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0360-2024·2024-03-06

    PROBLEND Hand Sanitizer Recalled Due to Manufacturing Deficiencies

    Seatex LLC is recalling PROBLEND Hand Sanitizer (Lot 266029) nationwide due to manufacturing deficiencies identified during FDA inspection.

    Product
    PROBLEND Hand Sanitizer, Refreshing Gel Hand Sanitizer, Ethanol 70% v/v Antiseptic, mountain spring scent, 1250 mL cases, Seatex LLC, 445 TX Hwy 36 Rosenberg, YX 77471
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1189-2024·2024-03-06

    Abbott Vysis Diagnostic Kits Recalled for U.S. Regulatory Non-Compliance

    Abbott Molecular recalls five Vysis in-vitro diagnostic kits that were intended for export and shipped to U.S. customers without approval or registration per U.S. specifications.

    Product
    In-vitro diagnostic kits: (1) Abbott Vysis LSI ATM (11q22.3) SpectrmOrange Probe, REF 01N33-020; (2) Abbott Vysis PTEN/CEP 10 FISH Probe Kit, REF 04N62-020; (3) Abbott Vysis TelVysion 1p SpectrumGreen Probe, REF 05J03-001; (4) Abbott Vysis TelVysion 4P SpectrumGreen Probe,
    Category
    Medical Device
    Distribution
    Distributed nationwide