Covidien Medtronic Invos Sensor Cable Recall: Error Codes or Non-Functioning
Covidien recalls reusable infant sensor adapter cables for Medtronic Invos PM7100 monitors due to manufacturing defects causing error codes or non-functioning channels. Affected units have specific lot numbers and UDI codes.
Lower-risk recall
manufacturing defects to sensor cable connectors may result in error codes or non-functioning channel
Contact the company
What happened, in plain English
Covidien is recalling reusable infant sensor adapter cables for Medtronic Invos monitors. These cables may cause error codes or stop working, which could lead to inaccurate monitoring of an infant's health. Read more at govinfonow.com/recall/56350-covidien-medtronic-invos-sensor-cable-recall-error-codes-or-non.
Source Summary by GovInfoNow · govinfonow.com/recall/56350-covidien-medtronic-invos-sensor-cable-recall-error-codes-or-non · Updated August 17, 2026 · FDA enforcement record: FDA #Z-1731-2024
Cite this page
“Covidien Medtronic Invos Sensor Cable Recall: Error Codes or Non-Functioning.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/56350-covidien-medtronic-invos-sensor-cable-recall-error-codes-or-non. Based on FDA recall #Z-1731-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1731-2024%22&limit=1).
Why it’s dangerous
The cables have manufacturing defects in the connectors that can cause error codes or the channel to stop working. This means the monitor might not properly track an infant's vital signs, potentially leading to missed health issues.
Who’s affected
Parents or caregivers using Medtronic Invos monitors with the recalled sensor cables. Infants being monitored with these devices are at risk if the cable fails.
How to tell if you have this one
Check the lot numbers: 20221220 or 20230721. Look for the unique device identifier (UDI) 10884521806436 on the cable packaging or label.
- Brand
Covidien- Category
Medical device
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Ongoing- Distribution
US: AK AZ CA CT FL GA IA IN LA MA MD MI MN MO NC NY OH OK PA SC TN TX VA WA WI OUS: Australia Austria Belgium Canary Islands Chile Czech Republic Denmark Finland France Germany Guatemala Indonesia Ireland Italy Japan Korea, Republic Of Kuwait Lithuania Mayotte New Zealand Nicaragua Poland Portugal Romania Slovakia Spain Sweden Switzerland Taiwan United Kingdom
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| Z-1731-2024 | Medtronic Invos, Reusable Infant Sensor Adapter Cable for PM7100, REF: PMAC71RIC; Lot # 20221220 and 20230721; UDI: 10884521806436 | 1122 units |
| Z-1732-2024 | Medtronic Invos, Reusable Sensor Cable for PM7100, REF: PMAC71RSC; Lot # 2023-02-22, 2023-04-28, 2023-05-04, 2023-07-20; UDI: 10884521780125 | 2305 units |
What to do — step by step
Check Cable Lot Number
Look for lot numbers 20221220 or 20230721 on the cable packaging or label.
Where it went and when
Where it was distributed
Distributed in 25 states, and outside the U.S.
FDA distribution: “US: AK AZ CA CT FL GA IA IN LA MA MD MI MN MO NC NY OH OK PA SC TN TX VA WA WI OUS: Australia Austria Belgium Canary Islands Chile Czech Republic Denmark Finland France Germany Guatemala Indonesia Ireland Italy Japan Korea, Republic Of…” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Alaska, Arizona, California, Connecticut, Florida, Georgia, Indiana, Iowa, Louisiana, Maryland, Massachusetts, Michigan, Minnesota, Missouri, New York, North Carolina, Ohio, Oklahoma, Pennsylvania, South Carolina, Tennessee, Texas, Virginia, Washington, Wisconsin.
Recall timeline
FDA published this recall 4 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-1731-2024 (January 9, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1731-2024 to see it in context.
- Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.