The Recall Desk

State

Colorado product recalls

20,304 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.

10226–10250 of 20304

  • HighFDA (Devices)·Z-1144-2024·2024-02-28

    Philips Allura Xper Interventional X-ray System Display and Imaging Malfunction

    A framegrabber card malfunction in Philips Allura Xper interventional X-ray systems may cause display failures, preventing proper visualization of medical images and delaying procedures.

    Product
    Philips Allura Xper Interventional Fluoroscopic X-ray Systems, specifically the Disk Bay of the PC component of affected systems. Affected PCs: FlexVision PC Allura Xper Model Name - Model Number: Allura Xper FD10 722003 722010 722026; Allura Xper FD10/10 722005
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1168-2024·2024-02-28

    W&H Surgical Handpiece S-12 Recalled for Incorrect Laser Marking

    W&H Surgical handpiece S-12 devices were incorrectly laser marked with '1:1' instead of the correct '1:2' during production. 160 units are affected.

    Product
    W&H Surgical handpiece S-12. For Surgical treatment of dental hard tissue Model Number: 30061000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0327-2024·2024-02-28

    FDA Recalls Oseltamivir Phosphate Oral Suspension for Out-of-Specification Impurities

    Amneal Pharmaceuticals is recalling 46,037 bottles of Oseltamivir Phosphate Oral Suspension due to failed quality test results showing impurities and degradation. The FDA classified this as a Class II recall affecting nationwide distribution.

    Product
    OSELTAMIVIR PHOSPHATE — OSELTAMIVIR PHOSPHATE (OSELTAMIVIR PHOSPHATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereCPSC·24129·2024-02-22

    Machir Biometric Personal Safes Recalled Due to Lock Failure Risk

    Machir LLC recalled about 24,820 biometric personal safes because the biometric lock can fail and allow unauthorized access. The firm received 15 reports of the lock failing to secure safes, posing a serious injury hazard and risk of death if firearms are stored inside.

    Product
    Machir Biometric Personal Safes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·24130·2024-02-22

    Bulldog Biometric Firearm Safes Recalled Due to Lock Failure Risk

    Bulldog Cases is recalling about 33,500 Magnum Biometric Pistol Vaults because the biometric lock can fail and be opened by unauthorized users, creating a serious injury hazard and risk of death when firearms are stored in the safe.

    Product
    Bulldog Biometric Firearm Safes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·24128·2024-02-22

    MouTec Biometric Firearm Safes Recalled for Unauthorized Access Risk

    The CPSC is recalling about 2,200 MouTec brand biometric firearm safes because the biometric lock can be opened by unauthorized users, posing a serious injury hazard and risk of death. One incident involved a 6-year-old opening the safe, though no injuries have been reported.

    Product
    MouTec brand Biometric Firearm Safes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24127·2024-02-22

    Gun Safes with Failing Biometric Locks Recalled for Unauthorized Access Risk

    About 60,000 Awesafe biometric gun safes can fail to lock, allowing unauthorized users to open them. No injuries reported, but consumers should immediately stop using the biometric feature and use the key instead until they receive a free replacement.

    Product
    Awesafe Biometric Gun Safes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24125·2024-02-22

    IKEA ÅSKSTORM 40W USB Chargers Recalled for Burn and Electric Shock Risk

    IKEA is recalling about 22,600 ÅSKSTORM 40W USB Chargers because the cable can become damaged or break over time, creating burn and electric shock hazards. Consumers should stop using the chargers immediately and return them to any IKEA store for a full refund.

    Product
    ÅSKSTORM 40W USB Chargers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24739·2024-02-22

    Spring Spirit and Biloban Pack and Play Mattresses Recalled for Suffocation Hazard

    The CPSC has recalled Spring Spirit and Biloban pack and play mattresses sold on Amazon.com due to a suffocation hazard to infants. The mattresses violate federal safety regulations and lack required warnings and labels.

    Product
    Spring Spirit and Biloban Pack and Play Mattresses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24740·2024-02-22

    Polaris MATRYX Snowmobiles Recalled for Primary Clutch Failure Hazard

    Polaris is recalling Model Year 2022–2024 MATRYX snowmobiles with PATRIOT 650 and 850 engines because the primary clutch can fail and separate from the vehicle, creating an injury hazard. Polaris has received 109 reports of clutch failure, including one incident resulting in a laceration injury.

    Product
    Model Year 2022-2024 MATRYX Snowmobiles equipped with PATRIOT 650 and 850 Engines
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24123·2024-02-22

    JURLEA Area Rugs Recalled for Fire Hazard Violation

    About 230 JURLEA area rugs sold on Amazon violate federal flammability regulations and pose a fire hazard. No injuries have been reported. Consumers should stop using the rugs and contact the distributor for a refund.

    Product
    JURLEA Area Rugs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24124·2024-02-22

    EVAS 20-lb Propane Exchange Cylinders Recalled for Fire Hazard

    Worthington Enterprises is recalling about 146,160 EVAS 20-lb propane exchange cylinders that could leak gas and pose a fire hazard. Consumers should stop using them immediately and return them to AmeriGas for free replacement.

    Product
    EVAS 20-lb. propane exchange cylinders
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24126·2024-02-22

    Cascade Designs MSR Camping Cooking Pots Recalled for Burn and Scald Hazards

    Cascade Designs is recalling select MSR camping cooking pots because the handle can detach or become loose, spilling hot food and liquids and causing burn or scald injuries. The company has received 22 reports of handle problems, including two burn injuries.

    Product
    MSR camping cooking pots
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24738·2024-02-22

    Magik & Kover Pack and Play Mattresses Recalled for Suffocation Hazard

    Magik & Kover Pack and Play Mattresses sold on Amazon are being recalled because they violate federal safety regulations for crib mattresses and pose a suffocation hazard to infants. Consumers should immediately stop using the mattresses and contact the company for a refund.

    Product
    Magik & Kover Pack and Play Mattresses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0980-2024·2024-02-21

    Impella Cardiac Support Catheters: Risk of Left Ventricle Perforation

    Impella cardiac catheters are being recalled due to risk of left ventricle perforation during operator use. The FDA has classified this Class I recall affecting 91,914 units worldwide.

    Product
    Impella catheters - Intravascular micro axial blood pumps that support a patient's circulatory system. (1) Product Code 005042 - Impella 2.5 (2) Product Code 005062 - Impella 5.0 (3) Product Code 005082- Impella LD (7) Product Codes 0550-0008 and 1000100 - Impella 5.5 wit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1139-2024·2024-02-21

    BIOFIRE BCID2 Blood Culture Panel Recalled for False Positive Candida tropicalis Results

    BioFire Diagnostics recalls BIOFIRE BCID2 panels due to false positive Candida tropicalis detection when used with certain BD BACTEC culture vials. The vials contain non-viable organism DNA that triggers incorrect positive results.

    Product
    BIOFIRE Blood Culture Identification 2 (BCID2) Panel when used with: BD BACTEC Lytic Anaerobic medium BD BACTEC Peds Plus medium BD BACTEC Plus Aerobic medium BD BACTEC Plus Anaerobic medium BD BACTEC Standard Aerobic medium BD BACTEC Standard Anaerobic medium The BIO
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1089-2024·2024-02-21

    global Medium embryo culture media recalled for potential development impairment

    CooperSurgical is recalling three specific lots of global Medium embryo culture media distributed to fertility clinics worldwide due to performance issues that may impair embryo development during culture.

    Product
    global Medium, Model Numbers LGGG-020 (20mL bottle), LGGG-050 (50mL bottle), LGGG-100 (100mL bottle). Intended use: Culture of human embryos from zygote to blastocyst, embryo transfer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1073-2024·2024-02-21

    Philips Recalls ProxiDiagnost Radiography Systems for Patient Data Display and Security Issues

    Philips is recalling 20 ProxiDiagnost radiography/fluoroscopy systems due to two issues: potential display of previous patient images when scanning new patients, and a security vulnerability allowing unauthorized data access. No injuries have been reported.

    Product
    ProxiDiagnost upgrade- A Multi-functional general Radiography and Fluoroscopy (R/F) system Ref:706150
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1072-2024·2024-02-21

    Philips ProxiDiagnost N90 X-ray System Recall for Patient Data and Security Issues

    Philips is recalling 138 U.S. units of its ProxiDiagnost N90 radiography system due to two identified issues. The system may display incorrect patient images during scan transitions, and a security vulnerability could allow unauthorized data access with physical device access.

    Product
    ProxiDiagnost N90- A Multi-functional general Radiography and Fluoroscopy (R/F) system Ref: (1)706100 (2)706110
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1088-2024·2024-02-21

    Philips CombiDiagnost R90 Fluoroscopy Display May Show Previous Patient Images

    Philips CombiDiagnost R90 fluoroscopy systems may display a previous patient's images during radiography examination, potentially showing different image content, format, and size that could affect imaging accuracy.

    Product
    CombiDiagnost R90 1.1 (709031)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1078-2024·2024-02-21

    Skin Graft Carrier Recalled for Manufacturing Ratio Defect

    Zimmer Surgical Inc. is recalling 3:1 Dermacarrier skin graft carriers due to a manufacturing defect where the ridge pattern is 1.5:1 instead of 3:1, potentially causing tissue damage or additional grafting.

    Product
    3:1 Dermacarrier, Model Number 00219501300, skin graft carrier
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1069-2024·2024-02-21

    Captus 4000e Thyroid Uptake Systems spring failure poses fall risk

    Mirion Technologies recalls 467 Captus 4000e Thyroid Uptake Systems due to spring arm failure that can cause the collimator to fall, posing potential injury risk to patients and operators.

    Product
    Captus 4000e Thyroid Uptake Systems- Intended to be used by trained Nuclear Medicine Technologists or Nuclear Medicine Physicians to perform Thyroid Uptake Procedures. Models: 5430-30151, 5430-30152, and 5430-30154
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1083-2024·2024-02-21

    Portable X-ray system may move unexpectedly if improperly cleaned

    The MobileDiagnost wDR portable X-ray system may move unexpectedly if excessive liquid is used during cleaning. This affects 851 devices distributed nationwide.

    Product
    MobileDiagnost wDR, Model numbers 712001, 712002, 712004, 712006, and 712007
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1085-2024·2024-02-21

    Stryker Trevo Trak 21 Microcatheter Recalled for Unevaluated Intended Use

    Stryker, Inc. is recalling 63 units of the Trevo Trak 21 Microcatheter because the device instructions contain an intended use that has not been evaluated by the FDA.

    Product
    Stryker Neurovascular, Trevo Trak 21 Microcatheter, REF 90338, 0.021in X162cm
    Category
    Medical Device
    Distribution
    Distributed nationwide