Data Foundry

Medical device recalls 2014

ANSPACH***Modified QD11 Attachment with Soft Tissue Protector***Rx… — Class II medical device recall Z-1886-2014

Terminated recall by The Anspach Effort, Inc., reported 2014-07-02, distributed in AL, CA, FL, IA, IL, KY, MN, MS…. The Anspach Effort, Inc. in Palm Beach Gardens, FL is recalling their Anspach Custom Devices. The units were n

Recall numberZ-1886-2014
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmThe Anspach Effort, Inc., Palm Beach Gardens, FL, United States
Recall initiated2012-11-28
Classified2014-06-25
Reported by FDA2014-07-02
Terminated2014-08-07
DistributedAL, CA, FL, IA, IL, KY, MN, MS, NC, OH, OK, PA, TN, TX
Countries outside the USCA, HU, JP, KR, SE
Quantity6
Serial numbers20039501, 20039502, 20039601, 20039602, 20039701, 20039702
Model numbers98-0013, 98-0014

Product

ANSPACH***Modified QD11 Attachment with Soft Tissue Protector***Rx Only*** This device is intended to be used with Anspach Systems

Reason for recall

The Anspach Effort, Inc. in Palm Beach Gardens, FL is recalling their Anspach Custom Devices. The units were not manufactured consistently with Quality System requirements.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1886-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.