Boston Scientific, Small Peripheral Cutting BalloonTM… recallZ-2137-2013 · Boston Scientific Corporation · initiated Jul 31, 2013
Class II Terminated All recalls posted in September 2013
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from Boston Scientific Corporation or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was recalled
Boston Scientific is initiating a recall removal of the 4.0mm x 15mm size of Small Peripheral Cutting Balloon (Monorail and Over-the-Wire) Microsurgical Dilatation Devices and Flextome Cutting Balloon (Monorail and Over-the-Wire) Microsurgical Dilation Devices. Boston Scientific has determined that users may experience significant difficulty or inability to remove the protector cap from the devic
FDA root cause category: Process change control
What the company is doing
Boston Scientific sent an Urgent Medical Device Recall Removal letter dated July 30, 2013, to all affected consignees. The letter identified the product, the problem, and the action to be taken by the consignee. Consignees were advised that further distribution or use of the product should cease immediately, and to segregate the product and return it to Boston Scientific. Consignees were asked to complete and return the "Recall Removal Reply Verification Tracking Form". For questions consignees were instructed to contact their local Sales Representative. For questions regarding this recall call 763-494-2042.
Recall details
- Recall number
- Z-2137-2013
- Recall class
- Class II
- Status
- Terminated
- Initiated by the company
- Jul 31, 2013
- Posted by the FDA
- Sep 3, 2013
- Recalling firm
- Boston Scientific Corporation
- Quantity
- 1,331
- Product code
- LIT
- FDA submissions
- P950020
- Distribution
- Worldwide Distribution - USA including AL, AZ, AR, CA, CO, CT, DE, DC, FL, GA, ID, IL, IN, IA, KY, LA, MD, MA, MI, MN, MS, MO, MT, NE, NV,NH,NJ, NY, NC, ND, OH, OK, OR, PA, RI, SC,SC, TN, TX, UT, VA, WA, WV, and WI. Internationally to Algeria, Finland, Japan, Spain, Australia, France, Latvia, Sweden, Austria, Germany, Netherlands, Switzerland, Belgium, Great Britain, Norway, Taiwan, Brazil, Greece, Panama, Turkey, Canada, Hong Kong, Poland, Unit.Arab Emir., China, India, Russian Fed., Colombia, Ireland, Saudi Arabia, Czech Republic, Israel, South Africa, Denmark, Italy, and South Korea.
Product description
Boston Scientific, Small Peripheral Cutting BalloonTM, Sterilized using irradiation: The Peripheral Cutting Balloon Catheters are indicated for Percutaneous Transluminal Angioplasty (PTA) of obstructive lesions of synthetic or native arteriovenous dialysis fistulae. 1) 4.00mm x 15mm Small Peripheral Cutting BalloonTM MonorailTM Microsurgical Dilatation Device, UPN #001BPM4015140F0, Catalogue # BPM4015140F & UPN # M001PCBM4015140F0, Catalogue # PCBM4015140F. 2) 4.00mm x 15mm Small Peripheral Cutting BalloonTM Over-the-Wire Microsurgical Dilatation Device, UPN # M001PCBO4015140F0, Catalogue # PCBO4015140F.
Code information (models, lots, serial numbers)
UPN # 001BPM4015140F0, Catalogue #BPM4015140F. Lot#'s 15778169, 15735527, 15774378, 15788826, 15812347, 15824636, 15825277, 15836626, 15873338, 15891705, 15931291, 15945240, 16057260. UPN# M001PCBM4015140F0, Catalogue #PCBM4015140F, Lot #15756145. UPN # M001PCBO4015140F0, Catalogue #PCBO4015140F, Lot #'s 15688199, 15992736, 16066536, 16141255.
Other devices under the same FDA submission
37 devices cleared under P950020 — the recall does not name any of them by identifier. One submission often covers many models, so they may or may not be affected.
- Wolverine Coronary Cutting Balloon H74939401103000Boston Scientific Corporation · Catheter, percutaneous transluminal coronary angioplasty (ptca), cutting/scoring1 death36 reports
- Wolverine Coronary Cutting Balloon H74939401103500Boston Scientific Corporation · Catheter, percutaneous transluminal coronary angioplasty (ptca), cutting/scoring21 reports
- Wolverine Coronary Cutting Balloon H74939401104000Boston Scientific Corporation · Catheter, percutaneous transluminal coronary angioplasty (ptca), cutting/scoring19 reports
- Wolverine Coronary Cutting Balloon H74939401153000Boston Scientific Corporation · Catheter, percutaneous transluminal coronary angioplasty (ptca), cutting/scoring19 reports
- Wolverine Coronary Cutting Balloon H74939401153500Boston Scientific Corporation · Catheter, percutaneous transluminal coronary angioplasty (ptca), cutting/scoring19 reports
- Wolverine Coronary Cutting Balloon H74939401102500Boston Scientific Corporation · Catheter, percutaneous transluminal coronary angioplasty (ptca), cutting/scoring16 reports
- Wolverine Coronary Cutting Balloon H74939401154000Boston Scientific Corporation · Catheter, percutaneous transluminal coronary angioplasty (ptca), cutting/scoring15 reports
- Wolverine Coronary Cutting Balloon H74939401063000Boston Scientific Corporation · Catheter, percutaneous transluminal coronary angioplasty (ptca), cutting/scoring9 reports
- Wolverine Coronary Cutting Balloon H74939401062500Boston Scientific Corporation · Catheter, percutaneous transluminal coronary angioplasty (ptca), cutting/scoring8 reports
- Flextome® Cutting Balloon® H749CBM3400150Boston Scientific Corporation · Catheter, percutaneous transluminal coronary angioplasty (ptca), cutting/scoring7 reports
- Wolverine Coronary Cutting Balloon H74939401102000Boston Scientific Corporation · Catheter, percutaneous transluminal coronary angioplasty (ptca), cutting/scoring7 reports
- Wolverine Coronary Cutting Balloon H74939401152500Boston Scientific Corporation · Catheter, percutaneous transluminal coronary angioplasty (ptca), cutting/scoring7 reports
Other products in the same recall event
The FDA groups related products into one recall event (event 65919).
- Z-2138-2013 · TerminatedBoston Scientific, FlextomeTM Cutting BalloonTM, Sterilized using irradiation: 1) 4.00mm x 15mm FlextomeTM Cutting BalloonTM MonorailTM Microsurgical Dilatation Device, UPN #H74…
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 18, 2026. Text above is shown as published by the FDA.
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