Bard Peripheral Vascular Inc Bard Recovery Cone Removal System, Catalog Numbers: RC-15. The device is intended for use for percutaneously remove the recovery filter or facilitate the retrieval of foreign objects from the peripheral vascular system. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Bard Recovery Cone Removal System, Catalog Numbers: RC-15. The device is intended for use for percutaneously remove the recovery filter or facilitate the retrieval of foreign objects from the peripheral vascular system.
Brand
Bard Peripheral Vascular Inc
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
All lots with expiry dates between May 2008 and February 2011. Serial Numbers: GFPD1574 GFPD2170 GFPD1576 GFPD4227 GFPD1575 GFPD2171 GFPD4228 GFPD4229 GFPD4230 GFPD4723 GFPD4724 GFPD4725 GFPD4727 GFPD4728 GFPD4729 GFPD2172 GFPD4726 GFPE3233 GFPE3234 GFPE3236 GFPE3235 GFPE3238 GFPE3237 GFPE3239 GFPE3240 GFPE3241 GFPE3242 GFPE3243 GFPE3244 GFPE3245 GFPF2336 GFPF4114 GFPF4115 GFPF4116 GFPF4117 GFPF4118 GFPF4119 GFPF4121 GFPF4122 GFPF4123 GFPF4120 GFPF4124 GFPF4125 GFPF4126 GFPF4127 GFPF4108 GFPF4109 GFPF4110 GFPF4111 GFPF4112 GFPF4113 GFPH0443 GFPH0444 GFPH0445 GFPH0446 GFPH0449 GFPH0447 GFPH0448 GFPH0450 GFPH0451 GFPH0452 GFPH0453 GFPH0454 GFPH0455 GFPH0457 GFPH0456 GFPH0458 GFPK2806 GFPK2807 GFPK2808 GFPK2809 GFPK2810 GFPK2811 GFPK2812 GFPK2813 GFPK2814 GFPK2815 GFPK4721 GFPK4722 GFPL4248 GFPL4249 GFPL4250 GFPL4251 GFPL4252 GFPL4253 GFPL4254 GFPL4255 GFPL4256 GFPL4257 GFPL4258 GFPL4259 GFPL4261 GFPL4260 GFQA3500 GFQA3501 GFQA3502 GFQA3503 GFQA3504 GFQA3505 GFQA3512 GFQA3514 GFQA3516 GFQB1627 GFQB1628 GFQA3518 GFQB1629 GFQB1630 GFQB1631 GFQB3492 GFQB3493 GFQB3494 GFQB3495 GFQB3496 GFQB3497 GFQB3499 GFQB3498 GFQB3500 GFQB3501 GFQB3502 GFQB3503 GFQB3504 GFQB3505 GFQB3506 GFQC4378 GFQC4379 GFQC4382 GFQC4380 GFQC4381 GFQD0077 GFQD0078 GFQD0079 GFQD0080 GFQD0081 GFQD0082 GFQD2039 GFQD2038 GFQD2040 GFQD3742 GFQD3744 GFQD3745 GFQD3739 GFQD3740 GFQD3741 GFQD3746 GFQD3747 GFQD3749 GFQE4409 GFQE4410 GFQE4724 GFQE4725 GFQF0388 GFQF0389 GFQF0392 GFQF4296 GFQF4297 GFQF4288 GFQF4289 GFQG2518 GFQG2841 GFQG3368 GFQG3369 GFQG3370 GFQG3371 GFQG3367 GFQG3372 GFQH2309 GFQH3845 GFQH3846 GFQI0229 GFQI0230 GFQI0231 GFQI0232 GFQI3507 GFQI3508 GFQJ0020 GFQJ0442 GFQJ0443 GFQJ0444 GFQJ0445 GFQJ0446 GFQJ0432 GFQI3994 GFQI3995 GFQJ4114 GFQJ4115 GFQJ4637 GFQJ4638 GFQJ4641 GFQJ4642 GFQJ4646 GFQJ4644 GFQJ4645 GFQK3057 GFQK3788 GFQL0324 GFQL0249 GFQL0250 GFQL0322 GFQL0323 GFQL0711 GFQL2631 GFQL2632 GFQL0731 GFQL2633 GFQL4073 GFQL4074 GFQL4075 GFQL4076 GFQL4077 GFQL4078 GFRA3887 GFRA3888 GFRA5030 GFRA5031 GFRA5032 GFRB0123 GFRB0124 GFRC0529 GFRC0530 GFRC0531 GFRC0532 GFRC0533 GFRC0534 GFRC0535 GFRC2639 GFRC2628 GFRC2629 GFRC2631 GFRC2632 GFRC2633 GFRC2634 GFRC2635 GFRC2630 GFRC2636 GFRC2637 GFRC2638 GFRD3500 GFRD3501 GFRD3502 GFRE1347 GFRE1349 GFRE1350 GFRE1351 GFRE1422 GFRE1423 GFRE1424 GFRE4483 GFRE4484 GFRE4485 GFRE4486 GFRE4487 GFRE4488 GFRE4489 GFRE4490 GFRE4491 GFRE4492 GFRE4493 GFRE4494 GFRE4495 GFRE4496 GFRE4497 GFRE4498 GFRF3639 GFRF3640 GFRF3641 GFRF3642 GFRF3643 GFRF3644 GFRF3645 GFRF3646 GFRF3647 GFRF3648 GFRF3649 GFRG2502 GFRG2503 GFRG2505 GFRG2504 GFRG2506 GFRG2507 GFRG2508 GFRH4779 GFRH4781 GFRH4780 GFRH4783 GFRH4782 GFRH4784 GFRH4785 GFRH4786 GFRI0045 GFRI3372 GFRI3373 GFRJ4044 GFRI3380 GFRI3381 GFRJ4045 GFRI3379 GFRI3382 GFRI3383 GFRJ4046 GFRJ4047 GFRJ4048 GFRJ4049 GFRK3903 GFRK3904 GFRK3905 GFRL0039 GFSA2453 GFSA2452 GFSB0182
Bard Peripheral Vascular Inc is recalling Bard Recovery Cone Removal System, Catalog Numbers: RC-15. The device is intended for use for perc due to This action is being taken because the product has a potential for the handle to detach. The handle detachment may result in the device unable to retr. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
This action is being taken because the product has a potential for the handle to detach. The handle detachment may result in the device unable to retrieve the filter or foreign body.
Recommended Action
Per FDA guidance
On May 9, 2008, BARD began distribution of an Urgent Recall Notice with fax-back attachment to all customers in the United States via overnight carrier (FedEx). The Notice informed customers of the problem and the risks associated with the use of this product. The letter instructed their customers to check all inventory locations for the recalled product, remove and return affected product to BPV. The letter also asked their customers to share this information regarding the recall with physicians that perform procedures with the affected product at their facility. Once the product affected by the recall has been removed from their inventory, the customers were asked to contact the BPV Recall Coordinator at 1-800-321-4254 X 2727 to obtain a Return Authorization Number to facilitate replacement of the returned devices. A mailing label was enclosed to return the recalled product.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026