Curity All Purpose Sponges — Class II medical device recall Z-0957-2019
Terminated recall by Cardinal Health 200, LLC, reported 2019-03-06, distributed nationwide. Curity All Purpose Sponges were not sterilized and distributed
| Recall number | Z-0957-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Cardinal Health 200, LLC, Mansfield, MA, United States |
| Recall initiated | 2018-12-27 |
| Classified | 2019-02-26 |
| Reported by FDA | 2019-03-06 |
| Terminated | 2020-06-29 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, CO |
| Lot numbers | 18E190262 |
| Expiration dates | 2023-05 |
Product
Curity All Purpose Sponges, Non-woven, 4 Ply, 4" x 4" (10.2 cm x 10.2 cm) Product Code: 8044 - Product Usage: Ideal for applying ointments, prepping, wiping needles, cleaning slides and more Rayon/polyester blend construction Highly absorbent.
Reason for recall
Curity All Purpose Sponges were not sterilized and distributed
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-0957-2019. 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.