Bard Midstream Urine Collector with Rigid Funnel and Iodophor Prep… — Class II medical device recall Z-2943-2018
Terminated recall by Bard Medical Division, reported 2018-09-05, distributed in AR, CA, CO, FL, GA, IA, IL, IN…. Medline notified BMD that the Aplicare Povidone Iodine (PVP-I) Prep Pads were not meeting the iodine assay lev
| Recall number | Z-2943-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Bard Medical Division, Covington, GA, United States |
| Recall initiated | 2018-03-21 |
| Classified | 2018-08-25 |
| Reported by FDA | 2018-09-05 |
| Terminated | 2020-04-02 |
| Distributed | AR, CA, CO, FL, GA, IA, IL, IN, KS, LA, MA, MD, MI, MN, MO, MS, NC, NJ, NY, SC, TN, TX, UT, WA |
| Quantity | 131,950 |
| Reason classes | potency |
| Lot numbers | NGAP2619, NGAT0331, NGAT4059, NGAW1807, NGBS2822, NGZD3819, NGZE0787, NGZF0382, NGZF4111, NGZI1126 |
| Model numbers | 842802 |
Product
Bard Midstream Urine Collector with Rigid Funnel and Iodophor Prep Pads. Product Packaging: Three (3) PVP-I prep pads are packed into each urine collection kit carton along with a pre-connected drainage funnel, specimen container, funnel lid, specimen lid and a room label.
Reason for recall
Medline notified BMD that the Aplicare Povidone Iodine (PVP-I) Prep Pads were not meeting the iodine assay level requirements to support 36 month expiration dating.
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-2943-2018. 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.