Bio-PLASTY Cannula — Class II medical device recall Z-1372-2015
Terminated recall by Biologic Therapies, Inc, reported 2015-04-08, distributed in CA, FL, IL, MA, NJ, TX, WA. Devices are misbranded - failure to properly classify and obtain FDA clearance prior distribution
| Recall number | Z-1372-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Biologic Therapies, Inc, Ocala, FL, United States |
| Recall initiated | 2015-01-23 |
| Classified | 2015-04-02 |
| Reported by FDA | 2015-04-08 |
| Terminated | 2015-08-06 |
| Distributed | CA, FL, IL, MA, NJ, TX, WA |
| Quantity | 58 |
| Reason classes | labeling |
| Model numbers | BPC.105, BPC.45, BPC.60, BPC.80 |
Product
Bio-PLASTY Cannula (Needle)
Reason for recall
Devices are misbranded - failure to properly classify and obtain FDA clearance prior distribution
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-1372-2015. 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.