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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.
November 13, 2024Medical DevicesFDA
American Surgical Company, LLC recalls Americot 20-01S (1/4" x 1/4") or 6mm x 6mm: Neurological sponges for use in the protection of neural tissue during surg
Hazard: Product defect where the X-ray detectable barium strip (aka radio-opaque marker) becomes detached from the sponge (pattie). May delay surgical process as the surgeon may require extra time to remove the markers from the surgical field.
June 1, 2016Medical DevicesFDA
American Surgical Company recalls Mass Eye & Ear Finger Cot Nasal 2's Ref Number: 41-04 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Policot 1/2" x 2" Ref Number: 90-29 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Policot 1/2" x 1.5" Ref Number: 90-08 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Policot 1/2" x 1/2" Ref Number: 90-06 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Policot 1/4" x 1/4" Ref Number: 90-02 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Telfa 1" x 3" Ref Number: 80-13 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Telfa 1" x 1" Ref Number: 80-12 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Telfa 3/4" x 3" Ref Number: 80-11 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Telfa 1/2" x 3" Ref Number: 80-09 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Telfa 1/2" x 1.5" Ref Number: 80-08 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Telfa 1/2" x 1/2" Ref Number: 80-06 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Telfa 3/8" x 3" Ref Number: 80-05 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Cylindrical Sponges-Strung 1/2" x 1.5" Ref Number: 70-02 Product Usage: Neurosurgical and Nonneuros
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Uniqcot 1/2" x 2" Ref Number: 67-29 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Uniqcot 1/2" x 3" Ref Number: 67-09 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Uniqcot 1/2" x 1.5" Ref Number: 67-08 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Uniqcot 1/2" x 1/2" Ref Number: 67-06 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Uniqcot 1/4" x 1/4" Ref Number: 67-02 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Delicot X 9 mm x 50 mm Ref Number: 63x07 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Delicot X 6 mm x 50 mm Ref Number: 63x06 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Delicot-J 30 mm x 70 mm Ref Number: 63-10J (Japan Only) Product Usage: Neurosurgical and Nonneur
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Delicot 30 mm x 70 mm Ref Number: 63-10 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Delicot 20 mm x 60 mm Ref Number: 63-09 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Delicot-J 13 mm x 60 mm Ref Number: 63-08J (Japan only) Product Usage: Neurosurgical and Nonneurosu
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Delicot 13 mm x 60 mm Ref Number: 63-08 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Delicot 9 mm x 50 mm Ref Number: 63-07 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Delicot 6 mm x 50 mm Ref Number: 63-06 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Delicot 4 mm x 50 mm Ref Number: 63-05 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Hazard: Product packaging defective compromising sterility
June 1, 2016Medical DevicesFDA
American Surgical Company recalls American Surgical Delicot-J 15 mm x 20 mm Ref Number: 63-04J (Japan Only) Product Usage: Neurosurgical and Nonneuro
Hazard: Product packaging defective compromising sterility