The Recall Desk

State

Colorado product recalls

73,716 recalls have nationwide distribution and so reach Colorado. 6,951 additional recalls listed Colorado specifically in their distribution scope.

What the numbers show

Total
6,951
Critical
1,215
Severe
1,826
Most recent
2026-10-28

Of the 6,951 recalls naming Colorado we have scored against our rubric, 1,215 (17%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,826 (26%) are Severe.

Which agencies issued them

These figures cover only the 6,951 recalls whose distribution notice names Colorado specifically. The 73,716 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

176–200 of 80667

  • HighFDA (Devices)·Z-0170-2027·2026-10-21

    Medline Recalls Surgical Convenience Kits with Non-Conforming Cannula Components

    Medline is recalling 193,374 surgical convenience kits nationwide because the cannula components do not meet ISO 80369-7 dimensional requirements and may leak or break during use.

    Product
    Medline surgical convenience kits labeled as: 1) OPEN HEART CDS, Medline product number/SKU CDS840094R; 2) OPEN HEART CDS, Medline product number/SKU CDS840171AG; 3) MHC AV FISTULA, Medline product number/SKU DYNJ903705K; 4) PERIPHERAL VASC MAJR-LF, Medline product…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0177-2027·2026-10-21

    Medline Recalls Surgical Kits With Non-Conforming Cannula Components

    Medline Industries is recalling 1,900 surgical convenience kits because cannula components do not meet ISO 80369-7 standards and may leak or break during use.

    Product
    Medline surgical convenience kits labeled as: 1) NEURO-SPINE BASIN PACK, Medline Product Number/SKU DYNJ80055A; 2) AV SHUNT PACK-LF, Medline Product Number/SKU DYNJ24528M.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0151-2027·2026-10-21

    Baxter Recalls Likorall Overhead Lifts Due to Motor Shaft Breakage Risk

    Baxter Healthcare is recalling Likorall Overhead Lifts because a motor shaft breakage combined with reduced safety system performance may cause the lift strap to lower quickly, posing a risk of patient injury.

    Product
    Likorall Overhead Lifts Product Code: 3121001 Product Description: LIKORALL 200 Product Code: 3122005 Product Description: LIKORALL 242 ES, NATURAL Product Code: 3122005NA Product Description: LIKORALL 242 ES, NATURAL Product Code: 3122006 Product Description…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0139-2027·2026-10-21

    BD Phoenix Panel NMIC-312 recalled for classification error

    Becton Dickinson is recalling 553,625 BD Phoenix Panel NMIC-312 units nationwide because the CPO Ambler classification feature may misclassify Klebsiella pneumoniae.

    Product
    BD Phoenix Panel NMIC-312. Catalog Number: 449082.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·26V699000·2026-10-21

    Autocar Recalls Xpeditor Trucks for Fuel Hose Separation Risk

    Autocar is recalling 2022-2027 Xpeditor trucks with Cummins L9 engines because fuel hoses may separate, causing leaks, engine stalls, and fire risks.

    Product
    AUTOCAR — AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0171-2027·2026-10-21

    Medline Recalls Surgical Kits With Non-Conforming Cannula Components

    Medline Industries is recalling 8,374 surgical convenience kits nationwide because the cannula components do not meet ISO 80369-7 dimensional requirements and may leak or break during use.

    Product
    Medline surgical convenience kits labeled as: 1) VEIN HARVESTING PACK-LF, Medline product number/SKU DYNJ0826732J; 2) NBMC VASCULAR PACK-LF, Medline product number/SKU DYNJ0665837G; 3) AV FISTULA, Medline product number/SKU DYNJ900454C; 4) VEIN PACK SHD, Medline product…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0179-2027·2026-10-21

    Medline surgical kits recalled for non-conforming cannula components

    Medline is recalling 6,069 surgical convenience kits because the cannula components do not meet ISO 80369-7 dimensional requirements and may leak or break during use.

    Product
    Medline surgical convenience kits labeled as: 1) SPINAL CDS, Medline Product Number/SKU CDS940087AM; 2) CUSTOM CRANI, Medline Product Number/SKU DYNJ907697C; 3) FEM POP PACK-LF, Medline Product Number/SKU DYNJ0159820F; 4) AV FISTULA PACK, Medline Product Number/SKU…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·26V697000·2026-10-21

    Thomas Built Buses Recalls 2027 Saf-T-Liner C2 School Buses

    Daimler Trucks North America is recalling 2027 Thomas Built Buses Saf-T-Liner C2 school buses because a heater hose may rupture, causing hot coolant to leak and burn occupants.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0144-2027·2026-10-21

    Sarnova Recalls Curaplex Capnography Cannula Kits Due to Pediatric Parts

    Sarnova HC is recalling 2,500 Curaplex Capnography kits because they were assembled with pediatric nasal cannulas instead of adult ones.

    Product
    Curaplex Capnography EtCO2/O2 Oral/Nasal Cannula Multipack (10 pk), Item Number 670272-KIT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0174-2027·2026-10-21

    Medline Recalls Surgical Kits With Non-Conforming Cannula Components

    Medline is recalling 472 surgical convenience kits because the cannula components do not meet ISO 80369-7 requirements, which may cause leaking or breaking during use.

    Product
    Medline surgical convenience kits labeled as: 1) MAIN/LAPAROSCOPY TRANSPLA PACK, Medline product number/SKU DYNJ0656274AC; 2) MAIN/LAPAROSCOPY TRANSPLA PACK, Medline product number/SKU DYNJ0656274AB; 3) CATH LAB ENDO AAA, Medline product number/SKU DYNJ35312I; 4)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0183-2027·2026-10-21

    Medline recalls CONMED AirSeal Access Port kits due to overpressure alerts

    Medline is recalling 3,551 convenience kits containing CONMED AirSeal Access Ports because they may trigger erroneous overpressure alerts and system venting, potentially delaying or ending surgical procedures.

    Product
    Convenience Kits containing CONMED AirSeal Access Ports CHN GYN ONCOLOGY DYNJ906731K DYNJ906731L DYNJ906731N DAVINCI PROSTATECTOMY DYNJG901002A DYNJG901002B DYNJG901002C DYNJG901002D GENERAL DAVINCI DYNJG901004B DYNJG901004D…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0145-2027·2026-10-21

    Ferno-Washington Power F2 Powered Fastening System Recall for Firmware Issue

    Ferno-Washington is recalling 319 Power F2 Powered Fastening Systems due to a firmware issue that may cause intermittent loss of powered functionality, potentially delaying patient transport.

    Product
    Power F2 Powered Fastening System, Power F2, Item No. 0567093 used with Power X2 Stretchers, Power X2, Item No. 0015816 and PowerX2 Premium, Item No. 0015821
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0181-2027·2026-10-21

    Medline Recalls Convenience Kits Containing CONMED AirSeal Access Ports

    Medline is recalling 3,551 convenience kits containing CONMED AirSeal Access Ports due to potential for erroneous overpressure alerts and system venting during use.

    Product
    Convenience Kits containing CONMED AirSeal Access Ports HERNANDEZ DAVINCI ACC BUNDLE M DYNJ911258 KIT ROBOTICS UROLOGY PROSTATE DYKMBNDL116I ROBOTIC CHEST DYNJ910997 DYNJ910997A RR-DAVINCI PROSTATE ACCESSORY DYNJ63392D UROLOGY LAPAROSCOPIC - 51638…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0038-2027·2026-10-21

    Teva Recalls Metoclopramide Tablets Due to Foreign Object Presence

    Teva Pharmaceuticals is recalling Metoclopramide tablets because they may contain foreign tablets or capsules. The affected products were distributed nationwide.

    Product
    METOCLOPRAMIDE — METOCLOPRAMIDE (METOCLOPRAMIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0169-2027·2026-10-21

    Medline recalls cardiac surgery kits with non-conforming cannula components

    Medline Industries is recalling 1,834 cardiac surgery kits because cannula components do not meet ISO 80369-7 dimensional requirements, which may contribute to leaking or breaking during use.

    Product
    1) Product Name AUD OPEN HEART PACK, Medline Kit Number/SKU DYNJ22052I; 2) Product Name AV SHUNT PACK-MARYVIEW, Medline Kit Number/SKU DYNJ24528N; 3) Product Name AV SHUNT PACK-MARYVIEW, Medline Kit Number/SKU DYNJ24528O; 4) Product Name AV SHUNT PACK-MARYVIEW, Medline Kit…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0182-2027·2026-10-21

    Medline Recalls Convenience Kits Containing CONMED AirSeal Access Ports

    Medline Industries is recalling 3,551 convenience kits containing CONMED AirSeal Access Ports due to potential overpressure alerts and system venting that may delay or end procedures.

    Product
    Convenience Kits containing CONMED AirSeal Access Ports GENERAL DAVINCI DYNJG901004C LAP CHOLE DYNJ88071 ROBOTIC PACK DYNJ50474F
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0156-2027·2026-10-21

    Steris RAPICIDE PA Part A High-Level Disinfectant Recalled for Pressure Hazard

    Steris is recalling RAPICIDE PA Part A High-Level Disinfectant because a blocked vented cap may cause the bottle to swell and release vapor or liquid, potentially injuring users.

    Product
    RAPICIDE PA Part A High-Level Disinfectant, Model/Catalog Number: ML020117
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0186-2027·2026-10-21

    Intelerad IntelePACS Software Recalled for Image Display Mismatch

    Intelerad Medical Systems is recalling IntelePACS software versions because reported and displayed images may not match due to a web-browser issue.

    Product
    IntelePACS, InteleConnect Portal/Tech Portal Versions PACS-5-1-1-R102, PACS-5-2-1-R93, PACS-5-3-1-R83 through R128, PACS-5-4-1-R66 through R101, PACS-5-5-1-R50 through R89, PACS-5-6-1-R41 through R81, PACS-5-7-1-R21 through R61, PACS-5-8-1-R2 through R42, PACS-5-9-1-R8 through…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0180-2027·2026-10-21

    Medline recalls CONMED AirSeal Access Port kits due to pressure alert issues

    Medline Industries is recalling 3,551 convenience kits containing CONMED AirSeal Access Ports due to potential erroneous overpressure alerts and system venting.

    Product
    Convenience Kits containing CONMED AirSeal Access Ports ADVANCE LAPAROSCOPIC DYNJ911135 LAP CHOLE DYNJ911660 LAP NISSEN DYNJ911560 UROLOGY LAPAROSCOPIC - 51638 DYNJ908720A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0168-2027·2026-10-21

    Medline surgical convenience kits recalled for non-conforming cannula components

    Medline is recalling 3,125 surgical convenience kits because the cannula components do not meet ISO 80369-7 dimensional requirements and may leak or break during use.

    Product
    Medline surgical convenience kits labeled as: CABG AUXILIARY PACK, Medline Product Number/SKU DYNJ44925D
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0158-2027·2026-10-21

    Gore Viabil Short Wire Biliary Endoprosthesis Recalled for Incorrect Length Labeling

    W L Gore & Associates is recalling 32 units of GORE VIABIL Short Wire Biliary Endoprosthesis because they may be mislabeled with the incorrect length.

    Product
    Generic Name: GORE VIABIL Short Wire Biliary Endoprosthesis; Model/Catalog Number: VSWVH0808 and VSWVN1006 Product Description: The GORE VIABIL Short Wire Biliary Endoprosthesis is a flexible, self-expanding endoprosthesis designed to maintain luminal patency of the common…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0173-2027·2026-10-21

    Medline Recalls Surgical Convenience Kits with Non-Conforming Cannula Components

    Medline is recalling 620 surgical convenience kits because the cannula components do not meet ISO 80369-7 dimensional requirements, which may cause leaking or breaking during use.

    Product
    Medline surgical convenience kits labeled as: 1) EAR, Medline product number/SKU DYNJ909020B; 2) EAR, Medline product number/SKU DYNJ909020A; 3) CAROTID PACK, Medline product number/SKU DYNJ42922C; 4) EAR, Medline product number/SKU DYNJ909020; 5) FEM CAROTID PACK…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0143-2027·2026-10-21

    Boston Scientific Recalls NaviFlex LW Pusher and Advx Panc. Stent

    Boston Scientific is recalling 403 units of NaviFlex LW Pusher and Advx Panc. Stent devices due to an incorrect manufacturing feature.

    Product
    NaviFlex LW Pusher; Advx Panc. Stent 4/5F; Material Number (UPN): M00535030;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateNHTSA·26E075000·2026-10-21

    Nissan Recalls Spare Tire Kits with Incorrect Placard Information

    Nissan is recalling spare tire accessory kits for certain 2026 Sentra vehicles because the tire placard contains incorrect size and inflation information.

    Product
    EQUIPMENT:OTHER:LABELS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide