Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp — Class II medical device recall Z-0573-2022
Ongoing recall by Baxter Healthcare Corporation, reported 2022-02-16. Cleaning products, containing, but not limited to, hydrogen peroxide, bleach, alcohol, or antiseptic agents an
| Recall number | Z-0573-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Baxter Healthcare Corporation, Deerfield, IL, United States |
| Recall initiated | 2022-01-07 |
| Classified | 2022-02-08 |
| Reported by FDA | 2022-02-16 |
| Quantity | 61,290 units |
| Reason classes | packaging |
Product
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, 5C4482EJ
Reason for recall
Cleaning products, containing, but not limited to, hydrogen peroxide, bleach, alcohol, or antiseptic agents and solvent, such as those containing acetone, toluene, xylene, or cyclohexanone may cause damage, such as leaking or cracking, to the MiniCap Extended Life PD transfer sets.
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-0573-2022. 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.