DeRoyal ST — Class II medical device recall Z-1134-2014
Terminated recall by DeRoyal Industries Inc, reported 2014-03-12, distributed in AL, FL, IL, KS, NJ, OK, OR, TX…. Three lots of circumcision clamps were manufactured out of specification and as a result may not properly clam
| Recall number | Z-1134-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | DeRoyal Industries Inc, Powell, TN, United States |
| Recall initiated | 2014-01-16 |
| Classified | 2014-03-04 |
| Reported by FDA | 2014-03-12 |
| Terminated | 2015-10-13 |
| Distributed | AL, FL, IL, KS, NJ, OK, OR, TX, VA, WA |
| Quantity | 2,504 units |
| Reason classes | specification failure |
| Lot numbers | 33347799, 33423747, 33444071 |
| Model numbers | 32-1622 |
Product
DeRoyal ST. Circumcision Clamp, REF 32-1622, Size 1.3 cm, 1 Per Pack, Rx Only STERILE EO, distributed by DeRoyal Industries.
Reason for recall
Three lots of circumcision clamps were manufactured out of specification and as a result may not properly clamp at the surgical site completely.
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-1134-2014. 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.