Recall Z-2030-2017— The Anspach Effort, Inc.

Name: FDA recall Z-2030-2017
Creator: U.S. Food and Drug Administration
Published: 2016-10-06

Class II · Terminated

Class II FDA medical device recall by The Anspach Effort, Inc., initiated 2016-10-06, terminated 2019-07-26. It names one FDA 510(k) clearance: K011444. Product: 5.0cm Heavy Duty Short Attachment. 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

510(k) clearances named in this recall

1 on FDA's record

K011444 — ANSPACH EMAX DRILL SYSTEMThe Anspach Effort, Inc.·cleared 2001-08-08

K-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.

Product description

5.0cm Heavy Duty Short Attachment

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.