Z-1239-2015 Class II Terminated
FDA device recall Z-1239-2015 was initiated by CooperSurgical, Inc. on Feb 9, 2015 and is designated Class II. Reason for recall: Incorrect size printed on the Milex Pessary Kit packaging label The recall status is terminated (terminated Jan 15, 2016). Affected quantity: 95 units.
Recall Details
- Product Type
- Devices
- Report Date
- Mar 11, 2015
- Initiation Date
- Feb 9, 2015
- Termination Date
- Jan 15, 2016
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 95 units
Product Description
CooperSurgical PESSARY KIT-CUBE#2, 1-3/8 in , 35 mm Part Number: MXKPEC02
Reason for Recall
Incorrect size printed on the Milex Pessary Kit packaging label
Distribution Pattern
Nationwide Distribution
Code Information
Lot numbers: 144351, 142789
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-1239-2015
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 25, 2026