FDA Medical Device Recalls (openFDA)
Cook Incorporated: Roadrunner PC Hydrophilic Wire Guide, Hydrophilic Guidewire Reference Part Number/GPN: RPC-035145-0-5 G34131 RPC-035145 G18154 RPC-035145-5 G34132 RPC-038145-0-5 G34129 RFSPC-038145-0 G17539 RFSPC-035145 G17540 RPC-038145-0 G18155 RPC-035145-0 G18153 RFSPC-035145-0 G17542
- Recall number
- Z-1837-2022
- Recalling firm
- Cook Incorporated
- Product
- Roadrunner PC Hydrophilic Wire Guide, Hydrophilic Guidewire Reference Part Number/GPN: RPC-035145-0-5 G34131 RPC-035145 G18154 RPC-035145-5 G34132 RPC-038145-0-5 G34129 RFSPC-038145-0 G17539 RFSPC-035145 G17540 RPC-038145-0 G18155 RPC-035145-0 G18153 RFSPC-035145-0 G17542
- Status
- Open, Classified
- Initiated
- 2022-08-16
- Posted
- 2022-09-28
- Terminated
- not on file
- Reason
- Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised.
- Root cause
- Under Investigation by firm
- Action
- On August 16, 2022, Cook Medical notified affected customers of the recall. Customers were instructed to immediately cease all further distribution and use of the affected products. Affected product should be quarantined and returned to Cook Medical to receive product credit. If you have any questions or concerns, please contact Cook Medical Customer Relations at 800.457.4500 or 812.339.2235
- Quantity
- 56 US; 1033 OUS
- Distribution
- Domestic distribution nationwide. Foreign distribution worldwide.
- Lot, serial or model codes
- RPC-035145-0-5 G34131 UDI-DI: 00827002341319 Lot/Expiration Date: 14769270X 03-06-2025 14802181 20-06-2025 14816224 28-06-2025 14818488 29-06-2025 14818489 29-06-2025 14828627 06-07-2025 14828629 06-07-2025 RPC-035145 G18154 UDI-DI: 00827002181540 Lot/Expiration Date: 14770863 06-06-2025 14770864 06-06-2025 14813490 27-06-2025 14816227 28-06-2025 NS14770866 06-06-2025 NS14804982 21-06-2025 RPC-035145-5 G34132 UDI-DI: 00827002341326 Lot/Expiration Date: 14770872 06-06-2025 14810022 23-06-2025 14831440 07-07-2025 RPC-038145-0-5 G34129 UDI-DI: 00827002341296 Lot/Expiration Date: 14804972 21-06-2025 14809971 23-06-2025 RFSPC-038145-0 G17539 UDI-DI: 00827002175396 Lot/Expiration Date: 14809157 23-06-2025 14837048 12-07-2025 RFSPC-035145 G17540 UDI-DI: 00827002175402 Lot/Expiration Date: 14818484 29-06-2025 14818485 29-06-2025 14818490 29-06-2025 14840310 13-07-2025 RPC-038145-0 G18155 UDI-DI: 00827002181557 Lot/Expiration Date: 14819269 29-06-2025 14823406 01-07-2025 14832976 08-07-2025 NS14828649 06-07-2025 RPC-035145-0 G18153 UDI-DI: 00827002181533 Lot/Expiration Date: 14828625 06-07-2025 14828630 06-07-2025 14828635 06-07-2025 14828636 06-07-2025 14828637 06-07-2025 14828640 06-07-2025 14828641 06-07-2025 14841469 14-07-2025 NS14813479 27-06-2025 NS14818486 29-06-2025 RFSPC-035145-0 G17542 UDI-DI: 00827002175426 Lot/Expiration Date: 14844152 15-07-2025
- 510(k) numbers
- ["K082536"]
- PMA numbers
- not on file
- Product code
- OCY
- Firm FEI
- 1820334
- Firm city
- Bloomington
- Firm state
- IN
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28