Overview of recall records associated with Cooper Surgical, Inc., including dates, categories and classifications where available.
Classification mix: Class III: 9, Class II: 2.
LEEP RediKit Products (for use in Loop Electrosurgical Excision Procedures) have Xylocaine (Lidocaine) HCL (2%) listed on the tray lid label but this is not included in the contents of the…
Pessary mislabeled outer package may not reflect the size of the product contained in the package
Pessary mislabeled outer package may not reflect the size of the product contained in the package
Pessary mislabeled outer package may not reflect the size of the product contained in the package
Pessary mislabeled outer package may not reflect the size of the product contained in the package
Incorrect size was printed on the outer product packaging.
Pessary mislabeled outer package may not reflect the size of the product contained in the package
Pessary mislabeled outer package may not reflect the size of the product contained in the package
Pessary mislabeled outer package may not reflect the size of the product contained in the package
Pessary mislabeled outer package may not reflect the size of the product contained in the package
Pessary mislabeled outer package may not reflect the size of the product contained in the package
This page summarizes recall records in which the official source identifies Cooper Surgical, Inc. 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.
