Medical DeviceJun 1, 2016
American Surgical Delicot-J 5 mm x 8 mm Ref Number: 63-01J (Japan Only) Product Usage recall — FDA Z-1777-2016
Product packaging defective compromising sterility
Class IIFDA: TerminatedAmerican Surgical Company
Recall history in this database
Classification mix: Class II: 91.
Medical DeviceJun 1, 2016
American Surgical Cotton Balls-Strung 1.25" Ref Number: 30-05 Product Usage: Neurosurgical recall — FDA Z-1758-2016
Product packaging defective compromising sterility
Class IIFDA: TerminatedAmerican Surgical Company
Medical DeviceJun 1, 2016
American Surgical Ray-Cot 1/2" x 2" Ref Number: 60-29 Product Usage: Neurosurgical and recall — FDA Z-1774-2016
Product packaging defective compromising sterility
Class IIFDA: TerminatedAmerican Surgical Company
Medical DeviceJun 1, 2016
American Surgical Cotton Balls-Strung 1/4" Ref Number: 30-00 Product Usage: Neurosurgical recall — FDA Z-1753-2016
Product packaging defective compromising sterility
Class IIFDA: TerminatedAmerican Surgical Company
Medical DeviceJun 1, 2016
American Surgical Telfa 1/2" x 3" Ref Number: 80-09 Product Usage: Neurosurgical and recall — FDA Z-1803-2016
Product packaging defective compromising sterility
Class IIFDA: TerminatedAmerican Surgical Company
Medical DeviceJun 1, 2016
American Surgical Telfa 1/2" x 1.5" Ref Number: 80-08 Product Usage: Neurosurgical and recall — FDA Z-1802-2016
Product packaging defective compromising sterility
Class IIFDA: TerminatedAmerican Surgical Company
Medical DeviceJun 1, 2016
American Surgical Delicot 30mm x 70mm Ref: 63-10 Product Usage: Neurosurgical and recall — FDA Z-1722-2016
Product packaging defective compromising sterility
Class IIFDA: TerminatedAmerican Surgical Company
Medical DeviceJun 1, 2016
American Surgical Ray-Cot 3" x 3" Ref Number: 60-15 Product Usage: Neurosurgical and recall — FDA Z-1772-2016
Product packaging defective compromising sterility
Class IIFDA: TerminatedAmerican Surgical Company
Medical DeviceJun 1, 2016
American Surgical Ray-Cot 1/2" x 1.5" Ref Number: 60-08 Product Usage: Neurosurgical and recall — FDA Z-1768-2016
Product packaging defective compromising sterility
Class IIFDA: TerminatedAmerican Surgical Company
Medical DeviceJun 1, 2016
American Surgical Delicot non-xray 5 mm x 8 mm Ref Number: 63-01 Non X-Ray Product Usage recall — FDA Z-1776-2016
Product packaging defective compromising sterility
Class IIFDA: TerminatedAmerican Surgical Company
Medical DeviceJun 1, 2016
American Surgical Ray-Cot 1/4" x 3" Ref Number: 60-04 Product Usage: Neurosurgical and recall — FDA Z-1765-2016
Product packaging defective compromising sterility
Class IIFDA: TerminatedAmerican Surgical Company
Medical DeviceJun 1, 2016
American Surgical Ultracot 5 mm x 8 mm (Glassine) Ref Number: 23-01G Product Usage recall — FDA Z-1737-2016
Product packaging defective compromising sterility
Class IIFDA: TerminatedAmerican Surgical Company
Medical DeviceJun 1, 2016
American Surgical Delicot-J 15 mm x 20 mm Ref Number: 63-04J (Japan Only) Product Usage recall — FDA Z-1783-2016
Product packaging defective compromising sterility
Class IIFDA: TerminatedAmerican Surgical Company
Medical DeviceJun 1, 2016
American Surgical Policot 1/2" x 1.5" Ref Number: 90-08 Product Usage: Neurosurgical and recall — FDA Z-1809-2016
Product packaging defective compromising sterility
Class IIFDA: TerminatedAmerican Surgical Company
Medical DeviceJun 1, 2016
American Surgical Ultracot 5 mm x 8 mm Ref Number: 23-01 Product Usage: Neurosurgical and recall — FDA Z-1736-2016
Product packaging defective compromising sterility
Class IIFDA: TerminatedAmerican Surgical Company
Medical DeviceJun 1, 2016
American Surgical Americot Blue 3/8" x 3/4" Ref Number: 20-14S Product Usage: Neurosurgical recall — FDA Z-1729-2016
Product packaging defective compromising sterility
Class IIFDA: TerminatedAmerican Surgical Company
Medical DeviceJun 1, 2016
American Surgical Ultracot 13 mm x 60 mm Ref Number: 23-08 Product Usage: Neurosurgical and recall — FDA Z-1744-2016
Product packaging defective compromising sterility
Class IIFDA: TerminatedAmerican Surgical Company
Medical DeviceJun 1, 2016
American Surgical Delicot 5 mm x 13 mm Ref Number: 63-02 Product Usage: Neurosurgical and recall — FDA Z-1778-2016
Product packaging defective compromising sterility
Class IIFDA: TerminatedAmerican Surgical Company
Medical DeviceJun 1, 2016
American Surgical Telfa 1" x 3" Ref Number: 80-13 Product Usage: Neurosurgical and recall — FDA Z-1806-2016
Product packaging defective compromising sterility
Class IIFDA: TerminatedAmerican Surgical Company
Medical DeviceJun 1, 2016
American Surgical Ultracot 9 mm x 50 mm (Glassine) Ref Number: 23-07G Product Usage recall — FDA Z-1743-2016
Product packaging defective compromising sterility
Class IIFDA: TerminatedAmerican Surgical Company
Medical DeviceJun 1, 2016
American Surgical Americot Blue 1/8" x 1/8" Ref Number: 20-19S Product Usage: Neurosurgical recall — FDA Z-1730-2016
Product packaging defective compromising sterility
Class IIFDA: TerminatedAmerican Surgical Company
Medical DeviceJun 1, 2016
American Surgical Ray-Cot 1" x 3" Ref Number: 60-13 Product Usage: Neurosurgical and recall — FDA Z-1771-2016
Product packaging defective compromising sterility
Class IIFDA: TerminatedAmerican Surgical Company
Medical DeviceJun 1, 2016
American Surgical Delicot-J 13 mm x 60 mm Ref Number: 63-08J (Japan only) Product Usage recall — FDA Z-1788-2016
Product packaging defective compromising sterility
Class IIFDA: TerminatedAmerican Surgical Company
Medical DeviceJun 1, 2016
American Surgical Telfa 1/2" x 1/2" Ref Number: 80-06 Product Usage: Neurosurgical and recall — FDA Z-1801-2016
Product packaging defective compromising sterility
Class IIFDA: TerminatedAmerican Surgical Company
Understanding this recall history
This page summarizes recall records in which the official source identifies American Surgical Company 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.