PlainRecalls
FDA Devices Moderate Class II Terminated

AL-III W/ male disconnect and 30ft hose Product Usage: Pneumatic system

Reported: May 10, 2017 Initiated: October 6, 2016 #Z-1932-2017

Product Description

AL-III W/ male disconnect and 30ft hose 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
17
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?
AL-III W/ male disconnect and 30ft hose Product Usage: Pneumatic system. Recalled by The Anspach Effort, Inc.. Units affected: 17.
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-1932-2017.