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American Surgical Recalls
92 recalls on record · June 1, 2016 to November 13, 2024 · Medical Devices
Recalls by year
16
24
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Ultracot 70 mm x 10090 mm Ref Number: 23-24 Product Usage: Neurosurgical and Nonneurosurgical Spon
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Ultracot 30 mm x 90 mm (Glassine) Ref Number: 23-15G Product Usage: Neurosurgical and Nonneurosurgi
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Ultracot 15 mm x 15 mm (Glassine) Ref Number: 23-12G Product Usage: Neurosurgical and Nonneurosurgi
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Ultracot 30 mm x 70 mm (Glassine) Ref Number: 23-10G Product Usage: Neurosurgical and Nonneurosurgi
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Ultracot 30 mm x 70 mm Ref Number: 23-10 Product Usage: Neurosurgical and Nonneurosurgical Spong
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Ultracot 20 mm x 60 mm (Glassine) Ref Number: 23-09G Product Usage: Neurosurgical and Nonneurosurgi
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Ultracot 20 mm x 60 mm Ref Number: 23-09 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Ultracot 13 mm x 60 mm (Glassine) Ref Number: 23-08G Product Usage: Neurosurgical and Nonneurosurgi
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Ultracot 13 mm x 60 mm Ref Number: 23-08 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Ultracot 9 mm x 50 mm (Glassine) Ref Number: 23-07G Product Usage: Neurosurgical and Nonneurosurgi
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Ultracot 6 mm x 50 mm Ref Number: 23-06 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Ultracot 15 mm x 20 mm (Glassine) Ref Number: 23-04G Product Usage: Neurosurgical and Nonneurosurgi
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Ultracot 15 mm x 20 mm Ref Number: 23-04 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Ultracot 10 mm x 13 mm (Glassine) Ref Number: 23-03G Product Usage: Neurosurgical and Nonneurosurgi
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Ultracot 5 mm x 13 mm (Glassine) Ref Number: 23-02G Product Usage: Neurosurgical and Nonneurosurgic
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Ultracot 5 mm x 8 mm (Glassine) Ref Number: 23-01G Product Usage: Neurosurgical and Nonneurosurgica
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Ultracot 5 mm x 8 mm Ref Number: 23-01 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Americot Blue 1/2" x 2" Ref Number: 20-32S Product Usage: Neurosurgical and Nonneurosurgical Sponge
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Americot White 1.5 cm x 5.5 cm Ref Number: 20-31SW Product Usage: Neurosurgical and Nonneurosurgic
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Americot Blue 1/4" x 1.5" Ref Number: 20-30S Product Usage: Neurosurgical and Nonneurosurgical Sp
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Americot Blue 3/8" x 2" Ref Number: 20-26S Product Usage: Neurosurgical and Nonneurosurgical Sponge
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Americot Blue 3/8" x 3/8" Ref Number: 20-22S Product Usage: Neurosurgical and Nonneurosurgical Spon
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Americot Blue 1/8" x 1/8" Ref Number: 20-19S Product Usage: Neurosurgical and Nonneurosurgical Spon
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Americot Blue 3/8" x 3/4" Ref Number: 20-14S Product Usage: Neurosurgical and Nonneurosurgical Spon
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Americot Blue 1" x 3" Ref Number: 20-10S Product Usage: Neurosurgical and Nonneurosurgical Sponges
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Americot Blue 1/2" x 3" Ref Number: 20-07S Product Usage: Neurosurgical and Nonneurosurgical Sponge
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Americot Blue 1/2" x 1.5" Ref Number: 20-06S Product Usage: Neurosurgical and Nonneurosurgical Sp
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Americot Blue 1/2" x 1" Ref Number: 20-05S Product Usage: Neurosurgical and Nonneurosurgical Sponge
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Americot Blue 1/2" x 1/2" Ref Number: 20-04S Product Usage: Neurosurgical and Nonneurosurgical Spon
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Americot Blue 1/4" x 1/4" Ref Number: 20-01S Product Usage: Neurosurgical and Nonneurosurgical Spon
Hazard: Product packaging defective compromising sterility