PlainRecalls
FDA Devices Moderate Class II Terminated

19cm Attachment, Black Max Product Usage: Pneumatic system

Reported: May 10, 2017 Initiated: October 6, 2016 #Z-1940-2017

Product Description

19cm Attachment, Black Max Product Usage: Pneumatic system

Reason for Recall

Supplied Directions for Use (DFU) did not contain a recommended service interval.

Details

Recalling Firm
The Anspach Effort, Inc.
Units Affected
41
Distribution
Worldwide Distribution - US Nationwide in the states of HI, DC including PR and the countries of Guam and Japan
Location
Palm Beach Gardens, FL

Frequently Asked Questions

What product was recalled?
19cm Attachment, Black Max Product Usage: Pneumatic system. Recalled by The Anspach Effort, Inc.. Units affected: 41.
Why was this product recalled?
Supplied Directions for Use (DFU) did not contain a recommended service interval.
Which agency issued this recall?
This recall was issued by the FDA Devices on May 10, 2017. Severity: Moderate. Recall number: Z-1940-2017.