Home › BOSTON SCIENTIFIC CORPORATION › Percuflex™
Percuflex™
BOSTON SCIENTIFIC CORPORATION · Model M001245750 · UDI-DI 08714729048671
FAD
Prescription
10
510(k) clearances
5,858
Adverse events (9 deaths)
55
Recalls
71
Facilities
Description
Ureteral Stent System Kit
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-11-06 | C.R. Bard Inc | Labeling discrepancy; Ureteral stent actual size may not match the actual product label. |
| 2025-11-06 | C.R. Bard Inc | Labeling discrepancy; Ureteral stent actual size may not match the actual product label. |
| 2025-11-06 | C.R. Bard Inc | Labeling discrepancy; Ureteral stent actual size may not match the actual product label. |
| 2025-11-06 | C.R. Bard Inc | Labeling discrepancy; Ureteral stent actual size may not match the actual product label. |
| 2022-07-29 | Hobbs Medical, Inc. | Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration |
| 2022-07-29 | Hobbs Medical, Inc. | Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration |
| 2022-07-29 | Hobbs Medical, Inc. | Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration |
| 2022-07-29 | Hobbs Medical, Inc. | Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration |
| 2022-07-29 | Hobbs Medical, Inc. | Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration |
| 2022-07-29 | Hobbs Medical, Inc. | Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.