Prytime Medical Devices recalls
Prytime Medical Devices appears in 2 official U.S. recall notices indexed by RecallRadar, most recently on 2021-02-17.
Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.
Recall summary
| Recall notices | 2 |
|---|---|
| Published | 2020-12-30 to 2021-02-17 |
| By agency | FDA Device (2) |
| By classification | Class II (2) |
| By status | terminated (2) |
| Distribution named in notices | US |
Recalls
- PRYTIME MEDICAL REBOA Catheter Introducer Kit, REF: KT1835C, Contents: Needle, 18 GA x 7 CM ECHOGENIC, STERILE, 1 EA, SYRINGE, 30CC, STERIL…
FDA Device · Class II · 2021-02-17 · Prytime Medical Devices
Reason: There is a potential that a catheter convenience set contains a 21G access needle instead of the correct 18G needle. If the 21G needle is used to gain vascular access then the guidewire included in the kit will not pass… - PryTime Medical - ER-Reboa Plus Catheter, Ref: ER7232PLUS, Guidewire Free, Compatabel with 7Fr introducer Sheaths, Arterial Line, Rx Only,…
FDA Device · Class II · 2020-12-30 · Prytime Medical Devices
Reason: There is a potential that catheters may have incorrectly marked balloon and arterial lines. This could result in a procedure delay or injury to the patient.