McKesson Lap Sponge — Class II medical device recall Z-2473-2021
Terminated recall by Cypress Medical Products LLC, reported 2021-09-22, distributed in VA. Manufacturer issued a recall due to an EO indicator color. The indicator should change from red to blue signif
| Recall number | Z-2473-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Cypress Medical Products LLC, Richmond, VA, United States |
| Recall initiated | 2021-08-11 |
| Classified | 2021-09-14 |
| Reported by FDA | 2021-09-22 |
| Terminated | 2023-07-07 |
| Distributed | VA |
| Lot numbers | CJJ12-07 |
| Model numbers | 16-2112121 |
Product
McKesson Lap Sponge, X-Ray Detectable 12"x 12", 5/pack, Sterile McKesson Part # 16-2112121
Reason for recall
Manufacturer issued a recall due to an EO indicator color. The indicator should change from red to blue signifying sterilization. However, on one case of product, the indicators did not change
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-2473-2021. 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.