BD MaxGuard Extension Set with 2 Needleless Y-Site — Class II medical device recall Z-1757-2022
Ongoing recall by CAREFUSION, reported 2022-09-28, distributed in AL, AR, AZ, CA, CO, FL, GA, IA…. Administration set, and extension set product labels list expiration year 2027 but the labels should list expi
| Recall number | Z-1757-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | CAREFUSION, San Diego, CA, United States |
| Recall initiated | 2022-08-01 |
| Classified | 2022-09-16 |
| Reported by FDA | 2022-09-28 |
| Distributed | AL, AR, AZ, CA, CO, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, NC, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, VT, WA, WV, WY |
| Quantity | 17,250 |
| Reason classes | labeling, packaging |
| UPC / GTIN / UDI-DI | 10885403237584 |
| Lot numbers | 22029431, 22029432 |
| Model numbers | MX9059 |
Product
BD MaxGuard Extension Set with 2 Needleless Y-Site, REF: MX9059
Reason for recall
Administration set, and extension set product labels list expiration year 2027 but the labels should list expiration year 2025. If expired product is used, the integrity of the product may be compromised, and may result in potential leaks and risk of infection to the patient and healthcare worker.
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-1757-2022. 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.