RegWardenFDA facility compliance records
Facility

Insulet Malaysia Sdn. Bhd.

15 recall(s) on record — most severe on record: Class I.

Activity by year

FDA actions on record by year2013: 1 recalls; 2015: 2 recalls; 2018: 1 recalls; 2020: 2 recalls; 2021: 1 recalls; 2022: 2 recalls; 2023: 2 recalls; 2025: 2 recalls; 2026: 2 recalls1’13’142’15’16’171’18’192’201’212’222’23’242’252’26
  • Recalls (15)

Devices registered here (1)

  • Alternate Controller Enabled Insulin Infusion Pump
    Product code QFG (opens in a new tab) · Class II · Clinical Chemistry · 21 CFR 880.5730

Recalls & enforcement

20262 records
  • Class IOngoing2026-05-20
    External soft cannula damage during manufacturing that results in insulin leaking around the Pod instead of being delivered to the user regardless of basal or bolus delivery. The primary failure mode is pump under-delivery due to loss of insulin to an external leak. If insulin is…
  • Class IOngoing2026-03-12
    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 delivery. This defect results from damage to the unexposed portio…
20252 records
  • Class IIOngoing2025-09-11
    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 single number on the keyboard. This causes the single digit numbe…
  • Class IIOngoing2025-05-23
    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 the user manually updates their phone settings to a region OUS …
20232 records
  • Class IOngoing2023-11-30
    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 the bolus calculator screen or the confirmation screen prior t…
  • Class IIOngoing2023-02-28
    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 may cause a delay in therapy. To reduce the volume of inquiries …
20222 records
  • Class IIOngoing2022-11-14
    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 Controller port. The excess heat may cause minor burns if touched,…
  • Class ITerminated2022-10-17
    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 result of thermal energy from a DASH PDM.
20211 record
  • Class IITerminated2021-02-01
    Certain foreign user guides include a misprint which could lead to an incorrect bolus delivery and hypoglycemia. Only Outside the US (OUS): Error in the Omnipod DASH User Guide text, page 6 of the User Guide, the text states that the comma (,) is not used for the decimal on the …
20202 records
  • Class IITerminated2020-04-02
    After the device has been in use for about 2 months, data processing in the PDM can be slowed such that the Bolus Calculator fails to accurately subtract the correct amout of IOB before suggesting a bolus amount.
  • Class IITerminated2020-02-13
    In certain scenarios, the Omnipod DASH PDM may suggest an inaccurate bolus amount based on a blood glucose value that is more than 10 minutes old when the user does not exit the bolus calculator as designed or when a system alarm interrupts a bolus calculation. If the user deliv…
20181 record
  • Class IITerminated2018-12-18
    There is a potential for a communication interruption following a bolus command that may result in inaccurate information presented in insulin on board (IOB), last bolus field or bolus history.
20152 records
  • Class ITerminated2015-11-02
    Pod's needle mechanism fails to deploy or there is a delay in the deployment of the needle mechanism.
  • Class ITerminated2015-07-13
    OmniPods® (Pods) have a higher rate of failure causing: Cannula fails to deploy/retract causing insulin to be pumped or the audible alarm is displayed on the PDM and pod will not deliver insulin
20131 record

Related

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Insulet Malaysia Sdn. Bhd. (FEI 3030970576) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3030970576-insulet-malaysia-sdn-bhd/

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