Covidien Medtronic Invos, Reusable Infant Sensor Adapter Cable for PM7100, REF: PMAC71RIC Recall
Hazard assessment based on recall description.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Medtronic Invos, Reusable Infant Sensor Adapter Cable for PM7100, REF: PMAC71RIC
Brand
Covidien
Lot Codes / Batch Numbers
Lot # 20221220 and 20230721, UDI: 10884521806436
Products Sold
Lot # 20221220 and 20230721; UDI: 10884521806436
Covidien is recalling Medtronic Invos, Reusable Infant Sensor Adapter Cable for PM7100, REF: PMAC71RIC due to manufacturing defects to sensor cable connectors may result in error codes or non-functioning channel. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
manufacturing defects to sensor cable connectors may result in error codes or non-functioning channel
Recommended Action
Per FDA guidance
On January 9, 2024 Medtronic (parent company of Covidien) issued a Urgent Medical Device Recall notification via UPS. Medtronic asked consignees to take the following action: 1. Quarantine and stop using all product from the affected lots of INVOS" Reusable Sensor Cables PMAC71RSC and PMAC71RIC. " See attachment A for guidance on how to identify affected devices via cable box packaging or cable hang tag. 2. Complete and return Customer Confirmation Form. Complete and return the enclosed Customer Confirmation Form even if you do not have any affected lots remaining. 3. Reach out to Medtronic to obtain RGA # /Returned Goods Authorization number. " Your Medtronic Representative / Medtronic Customer Service at rs.covidienfeedbackcustomerservice@medtronic.com can assist in initiating product return as necessary. 4. Return all product from the affected lots in your possession to Medtronic as described on the Customer Confirmation Form. 5. Pass on this notice to all those who need to be aware within your organization or to any organization where the potentially affected product from the specified lots has been transferred or distributed.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AK, AZ, CA, CT, FL, GA, IN, IA, LA, MD, MA, MI, MN, MO, NY, NC, OH, OK, PA, SC, TN, TX, VA, WA, WI
Page updated: Jan 10, 2026