Bioseal Corporation recalls Custom surgical kits labeled as follows: (a) Suture Removal Set, 910-0002 (b) Instrument Set, INST03/20 (c) Suture Re

Recalled November 15, 2017 · FDA recall Z-0085-2018 · Bioseal

Hazard

Custom surgical kits contain Aplicare Providone Iodine Prep Pads which were subsequently recalled by Medline Industries for in incorrect expiration date. · FDA Class II

Units

51635 units

Sold at

CA, IL, NC, VT

Description

Custom surgical kits contain Aplicare Providone Iodine Prep Pads which were subsequently recalled by Medline Industries for in incorrect expiration date.

Product

Custom surgical kits labeled as follows: (a) Suture Removal Set, 910-0002 (b) Instrument Set, INST03/20 (c) Suture Removal Set, SUT309/100 (d) Incision & Drainage Tray, INC03/20 (e) Suture Removal Set, SUT103/50 (f) General Purpose Tray, GPT010/25 (g) General Purpose Tray, GPT002/50

Manufacturer(s)

Bioseal Corporation

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →