Anspach REF: TURQ-434-4 Twist Drill for 1 — Class II medical device recall Z-0830-2014
Terminated recall by The Anspach Effort, Inc., reported 2014-02-05, distributed in CA, CO, IN, KY, MD, TX. Cutter was longer than was stated on the label
| Recall number | Z-0830-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | The Anspach Effort, Inc., Palm Beach Gardens, FL, United States |
| Recall initiated | 2011-03-31 |
| Classified | 2014-01-27 |
| Reported by FDA | 2014-02-05 |
| Terminated | 2019-07-18 |
| Distributed | CA, CO, IN, KY, MD, TX |
| Countries outside the US | DE, GB, JP, SE, TW |
| Quantity | 29 cutting |
| Reason classes | labeling |
| Lot numbers | D323038131, D343038845 |
| Model numbers | TURQ-434-4 |
Product
Anspach REF: TURQ-434-4 Twist Drill for 1.5mm x 4mm screw. Rx only Single use Sterile bone cutting burs.
Reason for recall
Cutter was longer than was stated on the label
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-0830-2014. 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.