Collagen Plugs — Class II medical device recall Z-0709-2022
Ongoing recall by Lacrimedics Inc, reported 2022-03-09, distributed nationwide. The sterile pouch seal may contain channels that could affect the seal integrity and potentially compromise st
| Recall number | Z-0709-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Lacrimedics Inc, Dupont, WA, United States |
| Recall initiated | 2022-01-17 |
| Classified | 2022-03-01 |
| Reported by FDA | 2022-03-09 |
| Distributed | Nationwide (US) |
| Countries outside the US | GB |
| Quantity | 4,780 units |
| Reason classes | sterility, packaging |
Product
Collagen Plugs, CP3, 0.3mm, CP4, 0.4mm, CP5, 0.5 mm, Sterile, EO, Rx Only, CE Dry eye treatment
Reason for recall
The sterile pouch seal may contain channels that could affect the seal integrity and potentially compromise sterility.
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-0709-2022. 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.