Akita Sumitomo Bakelite Co SB (Sumitomo Bakelite Co.,) Electrosurgical Knife Size: Working recall — FDA Z-0389-2017
Mislabeled product: Sterilization pouch and carton labeled as Standard Type instead of Short type
Overview of recall records associated with Akita Sumitomo Bakelite Co., Ltd., including dates, categories and classifications where available.
Classification mix: Class II: 2.
Mislabeled product: Sterilization pouch and carton labeled as Standard Type instead of Short type
Mislabeled product: Sterilization pouch and carton box labeled as Standard type instead of Jr type-Long
This page summarizes recall records in which the official source identifies Akita Sumitomo Bakelite Co., Ltd. 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.