Covidien Curity Eye Pad Item Code: 91650 The sterile eye pad is a… — Class II medical device recall Z-1741-2017
Terminated recall by Covidien LLC, reported 2017-04-12, distributed nationwide. Product sterility is compromised due to breach of sterile barrier
| Recall number | Z-1741-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Covidien LLC, North Haven, CT, United States |
| Recall initiated | 2017-03-03 |
| Classified | 2017-04-06 |
| Reported by FDA | 2017-04-12 |
| Terminated | 2019-10-07 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AU, BE, CA, CH, CZ, DK, EG, ES, FR, GB, GR, HU, IE, IL, IT, JP, KE, LU, MX, NL, NO, PH, PL, PT, RU, SA, SG, SK, ZA |
| Quantity | 1,659,500 |
| Reason classes | sterility |
| Model numbers | 91650 |
Product
Covidien Curity Eye Pad Item Code: 91650 The sterile eye pad is a device that consists of a pad made of various materials, such as gauze and cotton, intended for use as a bandage over the eye for protection or absorption of secretions. It is supplied sterile to allow for use in the operating room, and for application to the eye following injury and or surgery in order to reduce the likelihood of introduction of infection
Reason for recall
Product sterility is compromised due to breach of sterile barrier
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-1741-2017. 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.