Z-0775-2019 Class II Terminated
FDA device recall Z-0775-2019 was initiated by Wilson-Cook Medical Inc. on Dec 18, 2018 and is designated Class II. Reason for recall: The product is being recalled because Captura Serrated Forceps with Spike (DBF-2.4SN-230SP-20-S) were mislabeled as Captura Serrated Large Forcep-No Spike (DBF-2.4SL-230-20-S) and Captura Serrated… The recall status is terminated (terminated Dec 14, 2020). Affected quantity: 6 units.
Recall Details
- Product Type
- Devices
- Report Date
- Feb 6, 2019
- Initiation Date
- Dec 18, 2018
- Termination Date
- Dec 14, 2020
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 6 units
Product Description
COOK MEDICAL Captura SERRATED LARGE FORCEP-NO SPIKE, 2.4 mm, 230 cm, DBF-2.4SL- 230-20-S
Reason for Recall
The product is being recalled because Captura Serrated Forceps with Spike (DBF-2.4SN-230SP-20-S) were mislabeled as Captura Serrated Large Forcep-No Spike (DBF-2.4SL-230-20-S) and Captura Serrated Large Forcep-No Spike (DBF-2.4SL-230-20-S) were mislabeled as Captura Serrated Forceps with Spike (DBF-2.4SN-230SP-20-S).
Distribution Pattern
France, Ireland, Japan
Code Information
Lot Number W4035257
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-0775-2019
- openFDA file date
- Oct 21, 2026
- Loaded by RegDataLab
- Oct 23, 2026