Recall Z-0398-2018— The Anspach Effort, Inc.
Class II · Terminated
Class II FDA medical device recall by The Anspach Effort, Inc., initiated 2017-09-29, terminated 2019-07-30. FDA's recall record names no specific 510(k) clearance for this event. Product: OSCILLATING SAW ATTACHMENT Surgical instrument motors and accessories/attachments are intended for use during surgical procedures to cut hard tissue or bone and soft tissue.. Reason: This voluntary recall was initiated because a veterinary unit was physically shipped in error to a non-veterinary customer account..
- Recalling firm
- The Anspach Effort, Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2017-09-29
- Terminated
- 2019-07-30
- Firm location
- Palm Beach Gardens, FL, United States
Product description
OSCILLATING SAW ATTACHMENT Surgical instrument motors and accessories/attachments are intended for use during surgical procedures to cut hard tissue or bone and soft tissue.
Reason for recall
This voluntary recall was initiated because a veterinary unit was physically shipped in error to a non-veterinary customer account.
Data sourced from openFDA. This site is unofficial and independent of the FDA.