Vygon U.S.A. recalls
Every recall we track for Vygon U.S.A. — 11 in all, from 2018–2021 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Vygon U.S.A. peaked in 2018 (10); 11 since 2017.
All FDA recall records for Vygon U.S.A. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 10 | 0 | 10 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 1 | 0 | 1 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
Most common reasons for Vygon U.S.A. recalls
What to do if you have a recalled Vygon U.S.A. product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Vygon U.S.A. recalls
3 shown- Lower riskMedical device
Vygon U.S.A. recalls Vygon Dressing Change w/ Maxiswab - Product Usage: Custom Dressing Change kit, Product Code: AMS-8465CS.
Vygon recalls custom dressing change kits with potential infection risk due to sterile barrier failure. Affected kits have lot number 203373129 expiring June 30, 2022.
VygonApr 15, 2021 - Lower riskMedical device
Vygon U.S.A. recalls Vygon DUALSTOP Red Cap used for intravascular lines Product Code: 9888.00 - Product Usage: Cap used for intravascular
Vygon recalls DUALSTOP Red Caps for intravascular lines due to leaks. Product code 9888.00 with specific lot codes. Affected users should check their caps and contact Vygon for details.
VygonDec 6, 2018 - Lower riskMedical device
Vygon U.S.A. recalls PICC Tray, Product Code: AMS-9093CP Convenience kit for the insertion of PICCs into the vascular system.
Vygon recalls PICC Tray (AMS-9093CP) with lot numbers 16I026D and 16J032D due to potential friction holes that could compromise sterility. Affected users should contact Vygon for details.
VygonFeb 28, 2018
Vygon U.S.A. recall questions
How many recalls has Vygon U.S.A. had?
11 recalls from Vygon U.S.A. are on record with U.S. safety agencies, from 2018–2021.
What is the most recent Vygon U.S.A. recall?
Vygon U.S.A. recalls Vygon Dressing Change w/ Maxiswab - Product Usage: Custom Dressing Change kit, Product Code: AMS-8465CS., dated Apr 15, 2021. Every Vygon U.S.A. recall is listed on this page, newest first.
Why are Vygon U.S.A. products recalled?
The most common reasons on record: Potential friction holes may affect the sterility of the product. (8); DualStop Caps defect causing leaks in affected product (2).
What should I do if I have a recalled Vygon U.S.A. product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Vygon U.S.A. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.