Z-1732-2024 Class II Ongoing
FDA device recall Z-1732-2024 was initiated by Covidien on Jan 9, 2024 and is designated Class II. Reason for recall: manufacturing defects to sensor cable connectors may result in error codes or non-functioning channel The recall status is ongoing. Affected quantity: 2305 units.
Recall Details
- Product Type
- Devices
- Report Date
- May 8, 2024
- Initiation Date
- Jan 9, 2024
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 2305 units
Product Description
Medtronic Invos, Reusable Sensor Cable for PM7100, REF: PMAC71RSC
Reason for Recall
manufacturing defects to sensor cable connectors may result in error codes or non-functioning channel
Distribution Pattern
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
Code Information
Lot # 2023-02-22, 2023-04-28, 2023-05-04, 2023-07-20; UDI: 10884521780125
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-1732-2024
- openFDA file date
- Oct 26, 2026
- Loaded by RegDataLab
- Oct 27, 2026