Z-1625-2016 Class II Terminated
FDA device recall Z-1625-2016 was initiated by Stryker Sustainability Solutions on Apr 4, 2016 and is designated Class II. Reason for recall: Device packaging may not be sealed. The recall status is terminated (terminated Jul 13, 2016). Affected quantity: 4.
Recall Details
- Product Type
- Devices
- Report Date
- May 18, 2016
- Initiation Date
- Apr 4, 2016
- Termination Date
- Jul 13, 2016
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 4
Product Description
Mallinckrodt Evac Tracheal Tubes Model #124170-MALLINCKRODT & 124175
Reason for Recall
Device packaging may not be sealed.
Distribution Pattern
US distribution to KY.
Code Information
Lot #481938U
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-1625-2016
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 25, 2026