Drugs & medicalClass II

Insulet Corporation recalls Omnipod 5 Automated Insulin Delivery System Product catalog numbers: PT-000409: ASM, Omnipod 5, PDM, Programmed PT-000428: Adaptor,…

The firm has become aware of an issue with the Omnipod 5 Controller where the Controller charging port and charging cable are melting, deforming, or discoloring due to heat generated by increased resistance in the…

Read the official notice →
Date
2022-12-14
Country
United States
Brand
Insulet
Product
Omnipod 5 Automated Insulin Delivery System Product catalog numbers: PT-000409: ASM, Omnipod 5, PDM, Programmed PT-000428: Adaptor,…
Classification
Class II
Units
Domestic distribution nationwide.
Category
Drugs & medical
Source
FDA · Device

Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer

What to do

  1. Check the product name, strength and lot number against the official notice.
  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
  3. Ask the pharmacy or supplier about a replacement or refund.

General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.

More Insulet recalls

  1. 2026-04-22
  2. US
    Drugs & medicalClass I

    Insulet Corporation recalls Omnipod 5 Pods. Model/Catalog number: PT-001662 ASM 5PK Pod STRL OPS G6G7

    Due to a manufacturing defect, certain Omnipod 5 Pods from 49 lots have an internal soft cannula tear that results in insulin leaking into the Pod instead of being delivered to the user regardless of basal or bolus…

    FDA · DeviceInsulet CorporationNationwide distribution.Official notice →
  3. 2025-10-22
  4. US
    Drugs & medicalClass II

    Insulet Corporation recalls The failure occurs if a user on the Omnipod 5 iOS application selects and holds down on a manual entry field, to magnify the visual field…

    The failure occurs if a user on the Omnipod 5 iOS application selects and holds down on a manual entry field, to magnify the visual field using the magnifying feature of the iPhone, while simultaneously selecting a…

    FDA · DeviceInsulet CorporationUS Nationwide distribution.Official notice →
  5. 2025-07-02
  6. US
    Drugs & medicalClass II

    Insulet Corporation recalls Omnipod 5 Automated Insulin Delivery System, iOS Application. Model Number: PT-000664/M009-S-AP. Software Version: all Product…

    Insulet Corporation is recalling Omnipod 5 iOS App, due to a software design issue in which a comma is not recognized as a decimal separator and the user cannot enter a decimal separator in any manual entry screen if…

    FDA · DeviceInsulet CorporationUS market only- Although there are 122823 downloads of the application, our…Official notice →
  7. 2024-01-10
  8. US
    Drugs & medicalClass I

    Insulet Corporation recalls Omnipod 5 App (on compatible Android smartphones), Software Versions 1.1 - 1.2.3 (current). US: PT-000599- Omnipod 5 App Software Package…

    The bolus calculator is not recording the decimal point if it is the first value entered when changing a bolus dose. This may lead to an over-delivery of insulin to the user if the user does not recognize the error on…

    FDA · DeviceInsulet CorporationWorldwide distribution - US Nationwide and the countries of Germany and UK.Official notice →
  9. 2023-09-27
  10. US
    Drugs & medicalClass II

    Insulet Corporation recalls Omnipod 5 Automated Insulin Delivery System

    An error message was received when using the Omnipod 5 App on compatible smartphones that prevented phone control users from controlling the Omnipod 5 Automated Insulin Delivery System from their Omnipod 5 App which…

    FDA · DeviceInsulet CorporationDistribution throughout the USOfficial notice →
  11. 2022-11-23
  12. US
    Drugs & medicalClass I

    Insulet Corporation recalls 18239: ASM Omnipod Dash PDM, insulin delivery system. PT-000010: Assembly, Dash Final PDM U100, mg/dL PT-000011: Assembly, Dash Final PDM…

    The firm has become aware of PDM battery issues, including battery swelling, fluid leaking from the battery, and extreme overheating, which may pose a fire hazard. The firm has received a complaint alleging fire as a…

    FDA · DeviceInsulet CorporationWorldwide Distribution: US nationwide, Canada, Europe, Australia, and the…Official notice →
All 8 Insulet recalls →

Other drugs & medical recalls in the United States

  1. 2022-12-14
  2. US
    Drugs & medicalClass II

    Intersect ENT, Inc. recalls Propel Mini Mometasone Furoate Sinus Implant, with Straight Delivery System, REF 60044

    Sinus Implant product label displays incorrect product information including: "Straight Delivery System", with incorrect reference number and UDI-DI.

    FDA · DeviceIntersect ENT, Inc.US Nationwide distribution including in the states of NC, IL, KS, OR, WI, TX,…Official notice →
  3. US
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    Qvella Corporation recalls The FAST System and the FAST PBC Prep Cartridge together are a closed, rapid and automated sample preparation system for isolating…

    Device exceeds the limitations of a Class I 510(k)-exempt device so the user manual, instructions for use, and promotional materials are being corrected to remove all references to downstream applications.

    FDA · DeviceQvella CorporationUS: CA, NY, AL, UTOfficial notice →
  4. US
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    Olympus Corporation of the Americas recalls HF Resection Electrodes, Model Numbers WA22602S, WA22603S, WA22621S and WA22657S

    An incompatible HF cable may be packaged with the HF Resection Electrodes. This cable cannot be connected to the electrosurgical generator and may lead to delay or cancellation of the surgical procedure.

    FDA · DeviceOlympus Corporation of the AmericasUS Nationwide domestic distribution.Official notice →
  5. US
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    Getinge Usa Sales Inc recalls Flow-c Anesthesia System (Product Code 6887700) Flow-e Anesthesia System (Product Code 6887900)

    The power backup battery, under certain conditions, may exhibit reduced battery run-time while in use, and there is a potential that the battery may fail to provide the expected run time in the event of a mains power…

    FDA · DeviceGetinge Usa Sales IncUS Nationwide distribution in the states of CO, FL, IN, MA, MO, and VA.Official notice →
  6. US
    Drugs & medicalClass II

    Integrity Implants Inc. recalls LineSider Spinal System pedicle screws, 5.5/6.0mm, Non-mod Standard 7.1mm - Dual Lead, Non-cannulated. Model Number LS-N6SG6545.…

    Potential for intraoperative screw head separation at weld location.

    FDA · DeviceIntegrity Implants Inc.US distribution to California, Indiana, New York, Oklahoma, Washington DCOfficial notice →
  7. US
    Drugs & medicalClass II

    Integrity Implants Inc. recalls LineSider Spinal System 5.5/6.0mm, Non-mod Standard 7.1mm - Dual Lead, Cannulated. Thoracolumbosacral pedicle screw system; Spinal…

    Potential for weld separation of the Upper Tulip Head component from the Lower Tulip Head component, which would result in the separation of the Tulip Head from the Screw Shank.

    FDA · DeviceIntegrity Implants Inc.Nationwide distribution to AZ, CA, CT, DC, FL, IL, IN, LA, MA, MN, NJ, OK, PR,…Official notice →
See all drugs & medical recalls →