FDA Device recall Z-2177-2026
BARD Dynamic Tip Steerable, Product Number 6DYNTP001
- FDA Device
- Class II
- ongoing
- Published 2026-05-20
On 2026-05-20 the FDA classified a Class II recall of BARD Dynamic Tip Steerable, Product Number 6DYNTP001 by Stryker Sustainability Solutions, citing incomplete seals on sterile product.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2177-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-04-10 |
| Published | 2026-05-20 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Stryker Sustainability Solutions |
| Distribution | US |
Product
BARD Dynamic Tip Steerable, Product Number 6DYNTP001;
Reason
Incomplete seals on sterile product
Identifiers
| code_info | UDI 00885825005528, Lot Numbers: 3495675, 4117216, 4330131, 4471121, 4553575, 4630179, 4768595, 4821705, 4954755, 5043…UDI 00885825005528, Lot Numbers: 3495675, 4117216, 4330131, 4471121, 4553575, 4630179, 4768595, 4821705, 4954755, 5043512, 3684287, 4129638, 4334639, 4471122, 4554838, 4630180, 4773075, 4821706, 4954759, 5043513, 3691298, 4145046, 4334644, 4474949, 4555860, 4634858, 4793018, 4821707, 4961661, 5043514, 3763763, 4150788, 4334650, 4474951, 4556028, 4634859, 4793019, 4821708, 4971101, 5043515, 3775492, 4175981, 4355098, 4474952, 4569198, 4634860, 4793020, 4822439, 4971102, 5043518, 3775494, 4179878, 4359156, 4479369, 4569199, 4635785, 4793021, 4822440, 4973758, 5045769, 3784070, 4184227, 4359191, 4479371, 4569215, 4635862, 4793022, 4822455, 4974714, 5045901, 3792331, 4186482, 4359418, 4483403, 4570262, 4640440, 4794757, 4830178, 4976272, 5050564, 3794912, 4188323, 4367362, 4483440, 4576849, 4640444, 4794787, 4830179, 4976273, 5050565, 3794915, 4188326, 4367363, 4484604, 4581614, 4645476, 4794789, 4830180, 4976274, 5050573, 3812435, 4201950, 4375667, 4484728, 4583794, 4649445, 4795050, 483 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2177-2026%22
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