# FDA recall Z-0709-2022

> **Lacrimedics Inc** · Class II · device recall initiated 2022-01-17.

## 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.

## Distribution

Nationwide and Worldwide Distribution to following countries - AR. BE, BO, BR, CH, CN, CO, CZ, DE, EC, ES, FI, GE, IN, IL, MY, MX, NZ, PE, RO, SG, SA, TR, TW, TZ, UK

## Key facts

- **Recall number:** Z-0709-2022
- **Recalling firm:** Lacrimedics Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-01-17
- **Report date:** 2022-03-09

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Dupont, WA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0709-2022

## Citation

> AI Analytics. FDA recall Z-0709-2022. Retrieved 2026-06-04 from https://api.ai-analytics.org/recall/Z-0709-2022. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*