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Prytime Medical Devices Recalls
2 recalls on record · December 30, 2020 to February 17, 2021 · Medical Devices
Recalls by year
20
21
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
February 17, 2021Medical DevicesFDA
Prytime Medical Devices, Inc. recalls PRYTIME MEDICAL REBOA Catheter Introducer Kit, REF: KT1835C, Contents: Needle, 18 GA x 7 CM ECHOGENIC, STERILE, 1 EA,
Hazard: 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 through the access needle to facilitate insertion of an introducer sheath and could therefore cause procedure delay or injury.
December 30, 2020Medical DevicesFDA
Prytime Medical Devices, Inc. recalls PryTime Medical - ER-Reboa Plus Catheter, Ref: ER7232PLUS, Guidewire Free, Compatabel with 7Fr introducer Sheaths, Arter
Hazard: 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.