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.
FDA Recall Z-1218-2019 · Posted None
Advertisement
Recalling FirmSmiths Medical ASD Inc.
Recall StatusTerminated
Product CodeFOZ
Date Initiated2018-08-22
Date Terminated2021-02-11
Product Quantity136,600 units
Reason for Recall
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.
Firm 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 [email protected]. 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: [email protected].
Root Cause
Process design
Distribution Pattern
Worldwide Distribution: US (nationwide) and countries of: Canada, Australia, and New Zealand.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
Advertisement