Recall Z-1937-2017— The Anspach Effort, Inc.
Class II · Terminated
Class II FDA medical device recall by The Anspach Effort, Inc., initiated 2016-10-06, terminated 2019-07-26. FDA's recall record names no specific 510(k) clearance for this event. Product: Autolube-III with Foot Guard Product Usage: Pneumatic system. Reason: Supplied Directions for Use (DFU) did not contain a recommended service interval..
- Recalling firm
- The Anspach Effort, Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2016-10-06
- Terminated
- 2019-07-26
- Firm location
- Palm Beach Gardens, FL, United States
Product description
Autolube-III with Foot Guard Product Usage: Pneumatic system
Reason for recall
Supplied Directions for Use (DFU) did not contain a recommended service interval.
Data sourced from openFDA. This site is unofficial and independent of the FDA.