Recall Z-2535-2017— Cook Inc.
Class II · Terminated
Class II FDA medical device recall by Cook Inc., initiated 2017-04-25, terminated 2019-03-26. FDA's recall record names no specific 510(k) clearance for this event. Product: Pereyra Ligature Carrier 75. Reason: reprocessing instructions do not provide sufficient detailed information for the cleaning, disinfection, and sterilization of these products.
- Recalling firm
- Cook Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2017-04-25
- Terminated
- 2019-03-26
- Firm location
- Bloomington, IN, United States
Product description
Pereyra Ligature Carrier 75
Reason for recall
reprocessing instructions do not provide sufficient detailed information for the cleaning, disinfection, and sterilization of these products
Data sourced from openFDA. This site is unofficial and independent of the FDA.