Medcomp 15 — Class II medical device recall Z-2940-2020
Terminated recall by Medical Components, Inc dba MedComp, reported 2020-09-16, distributed in AZ, CA, FL, GA, NC, ND, NJ, NY…. Kits were packaged with the incorrect size valve peelable introducer. The kits include a 15F instead of the co
| Recall number | Z-2940-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medical Components, Inc dba MedComp, Harleysville, PA, United States |
| Recall initiated | 2020-07-27 |
| Classified | 2020-09-06 |
| Reported by FDA | 2020-09-16 |
| Terminated | 2021-04-30 |
| Distributed | AZ, CA, FL, GA, NC, ND, NJ, NY, OH, PA, VA, WA |
| Quantity | 132 eaches |
| UPC / GTIN / UDI-DI | 00884908129304 |
| Lot numbers | MPCT670 |
| Model numbers | THD155024 |
| Expiration dates | 2020-12-20 |
Product
Medcomp 15.SF X 24CM Titan HD CATHETER (CUFF 19CM FROM TIP) Ref: THD155024
Reason for recall
Kits were packaged with the incorrect size valve peelable introducer. The kits include a 15F instead of the correct 16F valve peelable introducer
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-2940-2020. 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.