Z-0051-2014 Class II Terminated
FDA device recall Z-0051-2014 was initiated by Synergetics Inc on Jul 30, 2013 and is designated Class II. Reason for recall: One lot of 25 gauge Soft-Tip Disposable Cannulas are co-mingled with 23 gauge cannulas; the product is labeled as 25 gauge cannulas. The recall status is terminated (terminated Apr 7, 2014). Affected quantity: 48/6-cannula boxes.
Recall Details
- Product Type
- Devices
- Report Date
- Oct 30, 2013
- Initiation Date
- Jul 30, 2013
- Termination Date
- Apr 7, 2014
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 48/6-cannula boxes
Product Description
Synergetics 25 gauge Soft Tip Cannula, packaged in 6 units per box. Catalog number: 30.08.25. Single-use 25 gauge cannula used in vitreoretinal surgery.
Reason for Recall
One lot of 25 gauge Soft-Tip Disposable Cannulas are co-mingled with 23 gauge cannulas; the product is labeled as 25 gauge cannulas.
Distribution Pattern
Nationwide Distribution-USA including the states of MO, CO, KY, TN, NC, PA, IL CA, NY, IN, MI, LA, NJ and OH.
Code Information
Lot number: M222240
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-0051-2014
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 25, 2026