Prytime Medical Devices, Inc. recalls
Every recall we track for Prytime Medical Devices, Inc. — 2 in all, all from 2020 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
2 recalls since 2017.
All FDA recall records for Prytime Medical Devices, Inc. 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 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 2 | 0 | 0 | 2 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 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 |
What to do if you have a recalled Prytime Medical Devices, Inc. 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 Prytime Medical Devices, Inc. recalls
2 shown- Use cautionMedical device
Prytime Medical Devices, Inc. recalls PRYTIME MEDICAL REBOA Catheter Introducer Kit, REF: KT1835C, Contents: Needle, 18 GA x 7 CM ECHOGENIC, STERILE, 1 EA,
Prytime Medical recalls Reboa Catheter Introducer Kit (KT1835C) due to possible 21G needle instead of 18G. Using this wrong needle may cause procedure delays or injury during vascular access.
Prytime MedicalDec 14, 2020 - Use cautionMedical device
Prytime Medical Devices, Inc. recalls PryTime Medical - ER-Reboa Plus Catheter, Ref: ER7232PLUS, Guidewire Free, Compatabel with 7Fr introducer Sheaths,
Prytime Medical recalls ER-Reboa Plus Catheters with potential incorrect balloon marking, risking procedure delays or patient injury. Affected units have specific model and lot numbers.
Prytime MedicalOct 29, 2020
Prytime Medical Devices, Inc. recall questions
How many recalls has Prytime Medical Devices, Inc. had?
2 recalls from Prytime Medical Devices, Inc. are on record with U.S. safety agencies, from 2020.
What is the most recent Prytime Medical Devices, Inc. recall?
Prytime Medical Devices, Inc. recalls PRYTIME MEDICAL REBOA Catheter Introducer Kit, REF: KT1835C, Contents: Needle, 18 GA x 7 CM ECHOGENIC, STERILE, 1 EA,, dated Dec 14, 2020. Every Prytime Medical Devices, Inc. recall is listed on this page, newest first.
What should I do if I have a recalled Prytime Medical Devices, Inc. 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 Prytime Medical Devices, Inc. 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.