FDA Medical Device Recalls (openFDA)
Smiths Medical ASD Inc.: Jelco(R) ViaValve(TM) safety intravenous (I.V.) catheters, 18G x 1 1/4", Model Number REF 3265, MOD 10 The Jelco(R) ViaValve(TM) safety I.V. catheter is a sterile, non pyrogenic, single use, radiopaque intravascular catheter device used for the administration of medically prescribed fluids, designed to reduce the risk of accidental secondary needle sticks.
- Recall number
- Z-1218-2019
- Recalling firm
- Smiths Medical ASD Inc.
- Product
- Jelco(R) ViaValve(TM) safety intravenous (I.V.) catheters, 18G x 1 1/4", Model Number REF 3265, MOD 10 The Jelco(R) ViaValve(TM) safety I.V. catheter is a sterile, non pyrogenic, single use, radiopaque intravascular catheter device used for the administration of medically prescribed fluids, designed to reduce the risk of accidental secondary needle sticks.
- Status
- Terminated
- Initiated
- 2018-08-22
- Posted
- not on file
- Terminated
- 2021-02-11
- Reason
- Several lots of Jelco ViaValve" safety intravenous (I.V.) catheters exhibited a V shaped puncture at the base of the catheter near the hub due to an adjustment that was made in the manufacturing process.
- Root cause
- Process design
- Action
- Smiths Medical delivered an "URGENT MEDICAL DEVICE RECALL NOTICE" dated 8/22/2018 and accompanying Recall Response Forms via tracked mail on 08/22/2018 to all consignees who purchased potentially affected product. The notices describe the product, problem and actions to be taken. The consignees were instructed to do the following: 1. Locate affected Jelco ViaValve" safety I.V. catheters in your possession 2. Determine the number of affected devices in your possession and complete the Recall Response Form within 10 days of receipt, returning it to SmithsMedical6697@stericycle.com. The form must be returned even if you do not have any of the affected product in your possession. Product credit and/or replacement will be processed once the Recall Response Form is received and returned affected product has been verified. 3. All affected product must be returned to Stericycle for processing. Please include a copy of the completed Recall Response Form inside EACH BOX of returned product to facilitate processing. 4. DISTRIBUTORS: If you have distributed potentially affected product to your customers, please immediately notify them of this recall. If you have any questions, contact the Compliance Manager at 763-383-3310 or email to: fieldactions@smiths-medical.com.
- Quantity
- 136,600 units
- Distribution
- Worldwide Distribution: US (nationwide) and countries of: Canada, Australia, and New Zealand.
- Lot, serial or model codes
- Lot Numbers: 3584467, 3584468, 3584469, 3576073, 3576233, 3578511, 3578512
- 510(k) numbers
- ["K160235"]
- PMA numbers
- not on file
- Product code
- FOZ
- Firm FEI
- 3012307300
- Firm city
- Minneapolis
- Firm state
- MN
- 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
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
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