Medical DeviceAug 25, 2021
Epimed International NEO-KATH(TM) Caudal Set, REF 201-2430, Sterile recall — FDA Z-2313-2021
Potential for stylet to protrude from the distal end of the catheter
Class IIFDA: CompletedEpimed International
Recall history in this database
Classification mix: Class II: 4.
Medical DeviceAug 25, 2021
Epimed International NEO-KATH Epidural Catheter Set, REF 200-2430, Sterile recall — FDA Z-2312-2021
Potential for stylet to protrude from the distal end of the catheter
Class IIFDA: CompletedEpimed International
Medical DeviceMay 13, 2020
Epimed International R-F Injector Cannula. 18gx10cm-STERILE recall — FDA Z-1849-2020
Incorrect expiration date on introduction cannula packaging.
Class IIFDA: TerminatedEpimed International
Medical DeviceMay 13, 2020
Epimed International R-F Injector Cannula. 20gx10cm-STERILE recall — FDA Z-1850-2020
Incorrect expiration date on introduction cannula packaging.
Class IIFDA: TerminatedEpimed International
Understanding this recall history
This page summarizes recall records in which the official source identifies Epimed International as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.