Progressive Medical PMI Endoscopic Dissector with Kittner Tip — Class II medical device recall Z-0276-2013
Terminated recall by Progressive Medical Inc, reported 2012-11-21, distributed nationwide. Some of the sterile packages had broken seals.
| Recall number | Z-0276-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Progressive Medical Inc, Saint Louis, MO, United States |
| Recall initiated | 2011-12-09 |
| Classified | 2012-11-14 |
| Reported by FDA | 2012-11-21 |
| Terminated | 2012-11-14 |
| Distributed | Nationwide (US) |
| Quantity | 70 boxes |
| Reason classes | sterility |
| Lot numbers | 1108-01 |
Product
Progressive Medical PMI Endoscopic Dissector with Kittner Tip (5mm x 40cm), Reorder Number: PMILK40, Product Sterile in Unopened/Undamaged pouch, Cotton Tip - X-Ray Detectable, 1 Pc/Pouch, 10 Pouches/Box, 20 boxes/case. Exclusively Distributed in the U.S. Market by: Progressive Medical, Inc., St. Louis, MO, Made in China. The product is used for pushing tissue from the incision or wound during medical procedures. Per the IFU, the indications for use are for gynecological laparoscopy, laparoscopic cholecystectomy, and other laparoscopic procedures.
Reason for recall
Some of the sterile packages had broken seals.
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-0276-2013. 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.