Bard Magic 3 Antibacterial Hydrophilic Intermittent Catheter Female — Class II medical device recall Z-3226-2017
Terminated recall by C.R. Bard, Inc., reported 2017-10-04, distributed in AL, AZ, CA, FL, GA, IL, IN, KS…. Specific lots labeled as an Antibacterial Hydrophilic Intermittent Catheter may lack the hydrophilic coating.
| Recall number | Z-3226-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | C.R. Bard, Inc., Covington, GA, United States |
| Recall initiated | 2017-07-28 |
| Classified | 2017-09-27 |
| Reported by FDA | 2017-10-04 |
| Terminated | 2020-08-25 |
| Distributed | AL, AZ, CA, FL, GA, IL, IN, KS, KY, MA, MO, NC, NJ, NY, OH, OK, OR, PA, TN, TX, UT, VA, WA |
| Quantity | 45,270 units |
| Reason classes | labeling |
| Lot numbers | 53623024, 53623047, 53623054, 53623122 |
| Model numbers | 51514 |
| Expiration dates | 2020-01-31 |
Product
Bard Magic 3 Antibacterial Hydrophilic Intermittent Catheter Female, 14 FR (30/box), Rx Only intended for urinary bladder drainage in patients requiring catheterization for management of incontinence, voiding dysfunction, and surgical procedures.
Reason for recall
Specific lots labeled as an Antibacterial Hydrophilic Intermittent Catheter may lack the hydrophilic coating.
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-3226-2017. 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.