Recall Z-0813-2018— Alto Development Corp
Class II · Terminated
Class II FDA medical device recall by Alto Development Corp, initiated 2017-10-23, terminated 2019-04-30. FDA's recall record names no specific 510(k) clearance for this event. Product: Surgical punch; sealed pouches packed in punch shelf box Intended for use by trained surgeons to create circular cuts in soft tissue or openings in soft vessel walls during surgical procedures.. Reason: Surgical punches are being recalled due to potential packaging damage which may have occurred during transportation resulting in loss of sterility..
- Recalling firm
- Alto Development Corp
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2017-10-23
- Terminated
- 2019-04-30
- Firm location
- Wall Township, NJ, United States
Product description
Surgical punch; sealed pouches packed in punch shelf box Intended for use by trained surgeons to create circular cuts in soft tissue or openings in soft vessel walls during surgical procedures.
Reason for recall
Surgical punches are being recalled due to potential packaging damage which may have occurred during transportation resulting in loss of sterility.
Data sourced from openFDA. This site is unofficial and independent of the FDA.