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American Contract Systems Recalls
204 recalls on record · November 21, 2018 to May 13, 2026 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
August 14, 2024Medical DevicesFDA
American Contract Systems, Inc. recalls American Contract Systems Gyn Laparoscopy convenience kit
Hazard: Product released with insufficient aeration time impacting the kits sterilized on the same cycle or in the same aeration chamber, which may have been compromised in sterility
August 14, 2024Medical DevicesFDA
American Contract Systems, Inc. recalls American Contract Systems Hand Pack convenience kit
Hazard: Product released with insufficient aeration time impacting the kits sterilized on the same cycle or in the same aeration chamber, which may have been compromised in sterility
July 17, 2024Medical DevicesFDA
American Contract Systems Inc recalls KNEE ARTHROSCOPY PACK-Procedure Kit Catalog Number: WEKA15B
Hazard: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding component exceeded the residual limits for permanent exposure devices as indicated by ANSI/AAMI/ISO 10993-7/(R)2012.
July 17, 2024Medical DevicesFDA
American Contract Systems Inc recalls HAND PACK-Procedure Kit Catalog Number: WEHD16C
Hazard: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding component exceeded the residual limits for permanent exposure devices as indicated by ANSI/AAMI/ISO 10993-7/(R)2012.
July 17, 2024Medical DevicesFDA
American Contract Systems Inc recalls HAND PACK-Procedure Kit Catalog Number: WEHD16B
Hazard: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding component exceeded the residual limits for permanent exposure devices as indicated by ANSI/AAMI/ISO 10993-7/(R)2012.
July 17, 2024Medical DevicesFDA
American Contract Systems Inc recalls ORIF HIP - IM RODDING FEMUR-Procedure Kit Catalog Number: UTHP44S
Hazard: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding component exceeded the residual limits for permanent exposure devices as indicated by ANSI/AAMI/ISO 10993-7/(R)2012.
July 17, 2024Medical DevicesFDA
American Contract Systems Inc recalls CUSTOM KNEE - 206061-Procedure Kit Catalog Number: UDKN68AG
Hazard: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding component exceeded the residual limits for permanent exposure devices as indicated by ANSI/AAMI/ISO 10993-7/(R)2012.
July 17, 2024Medical DevicesFDA
American Contract Systems Inc recalls CUSTOM KNEE - 206061-Procedure Kit Catalog Number: UDKN68AE
Hazard: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding component exceeded the residual limits for permanent exposure devices as indicated by ANSI/AAMI/ISO 10993-7/(R)2012.
July 17, 2024Medical DevicesFDA
American Contract Systems Inc recalls ACL PACK - 206039-Procedure Kit Catalog Number: UDAC66AA
Hazard: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding component exceeded the residual limits for permanent exposure devices as indicated by ANSI/AAMI/ISO 10993-7/(R)2012.
July 17, 2024Medical DevicesFDA
American Contract Systems Inc recalls TPK ANTERIOR HIP PACK 176483-Procedure Kit Catalog Number: TPAH21E
Hazard: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding component exceeded the residual limits for permanent exposure devices as indicated by ANSI/AAMI/ISO 10993-7/(R)2012.
July 17, 2024Medical DevicesFDA
American Contract Systems Inc recalls ARTHROSCOPY PACK-Procedure Kit Catalog Number: TNAR22V
Hazard: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding component exceeded the residual limits for permanent exposure devices as indicated by ANSI/AAMI/ISO 10993-7/(R)2012.
July 17, 2024Medical DevicesFDA
American Contract Systems Inc recalls ARTHROSCOPY PACK-Procedure Kit Catalog Number: TNAR22U
Hazard: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding component exceeded the residual limits for permanent exposure devices as indicated by ANSI/AAMI/ISO 10993-7/(R)2012.
July 17, 2024Medical DevicesFDA
American Contract Systems Inc recalls TOTAL KNEE-Procedure Kit Catalog Number: SMTK21C
Hazard: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding component exceeded the residual limits for permanent exposure devices as indicated by ANSI/AAMI/ISO 10993-7/(R)2012.
July 17, 2024Medical DevicesFDA
American Contract Systems Inc recalls KNEE ARTHROSCOPY-Procedure Kit Catalog Number: SLAR14G
Hazard: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding component exceeded the residual limits for permanent exposure devices as indicated by ANSI/AAMI/ISO 10993-7/(R)2012.
July 17, 2024Medical DevicesFDA
American Contract Systems Inc recalls HAND DRAPING SJH-Procedure Kit Catalog Number: SJHD67F
Hazard: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding component exceeded the residual limits for permanent exposure devices as indicated by ANSI/AAMI/ISO 10993-7/(R)2012.
July 17, 2024Medical DevicesFDA
American Contract Systems Inc recalls TOTAL KNEE-Procedure Kit Catalog Number: SFTK54B
Hazard: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding component exceeded the residual limits for permanent exposure devices as indicated by ANSI/AAMI/ISO 10993-7/(R)2012.
July 17, 2024Medical DevicesFDA
American Contract Systems Inc recalls KNEE ARTHROSCOPY PACK-Procedure Kit Catalog Number: SFAR60A
Hazard: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding component exceeded the residual limits for permanent exposure devices as indicated by ANSI/AAMI/ISO 10993-7/(R)2012.
July 17, 2024Medical DevicesFDA
American Contract Systems Inc recalls TOTAL KNEE - 297835 -Procedure Kit Catalog Number: RGTK10L
Hazard: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding component exceeded the residual limits for permanent exposure devices as indicated by ANSI/AAMI/ISO 10993-7/(R)2012.
July 17, 2024Medical DevicesFDA
American Contract Systems Inc recalls TOTAL KNEE - 297835-Procedure Kit Catalog Number: RGTK10K
Hazard: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding component exceeded the residual limits for permanent exposure devices as indicated by ANSI/AAMI/ISO 10993-7/(R)2012.
July 17, 2024Medical DevicesFDA
American Contract Systems Inc recalls HAND PACK 297829--Procedure Kit Catalog Number: RGHN04I
Hazard: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding component exceeded the residual limits for permanent exposure devices as indicated by ANSI/AAMI/ISO 10993-7/(R)2012.
July 17, 2024Medical DevicesFDA
American Contract Systems Inc recalls TOTAL KNEE -Procedure Kit Catalog Number: QPTK95B
Hazard: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding component exceeded the residual limits for permanent exposure devices as indicated by ANSI/AAMI/ISO 10993-7/(R)2012.
July 17, 2024Medical DevicesFDA
American Contract Systems Inc recalls TOTAL KNEE -Procedure Kit Catalog Number: QPTK95A
Hazard: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding component exceeded the residual limits for permanent exposure devices as indicated by ANSI/AAMI/ISO 10993-7/(R)2012.
July 17, 2024Medical DevicesFDA
American Contract Systems Inc recalls KNEE ARTHROSCOPY-Procedure Kit Catalog Number: QPKA35A
Hazard: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding component exceeded the residual limits for permanent exposure devices as indicated by ANSI/AAMI/ISO 10993-7/(R)2012.
July 17, 2024Medical DevicesFDA
American Contract Systems Inc recalls KNEE ARTHROSCOPY PACK Catalog Number: MEKA12R
Hazard: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding component exceeded the residual limits for permanent exposure devices as indicated by ANSI/AAMI/ISO 10993-7/(R)2012.
July 17, 2024Medical DevicesFDA
American Contract Systems Inc recalls TOTAL KNEE, ST LUKES Catalog Number: LMTK17AP
Hazard: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding component exceeded the residual limits for permanent exposure devices as indicated by ANSI/AAMI/ISO 10993-7/(R)2012.
July 17, 2024Medical DevicesFDA
American Contract Systems Inc recalls ACL, ST LUKES METHODIST 1CS Catalog Number: LMAC10AA
Hazard: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding component exceeded the residual limits for permanent exposure devices as indicated by ANSI/AAMI/ISO 10993-7/(R)2012.
July 17, 2024Medical DevicesFDA
American Contract Systems Inc recalls UPPER EXTREMITY PK, STRL F G Catalog Number: IHUE40AG
Hazard: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding component exceeded the residual limits for permanent exposure devices as indicated by ANSI/AAMI/ISO 10993-7/(R)2012.
July 17, 2024Medical DevicesFDA
American Contract Systems Inc recalls KNEE SCOPE Procedure tray Catalog Number: COKN48L
Hazard: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding component exceeded the residual limits for permanent exposure devices as indicated by ANSI/AAMI/ISO 10993-7/(R)2012.
July 17, 2024Medical DevicesFDA
American Contract Systems Inc recalls HAND WRIST FOREARM-LF Procedure tray Catalog Number: CCHD17B
Hazard: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding component exceeded the residual limits for permanent exposure devices as indicated by ANSI/AAMI/ISO 10993-7/(R)2012.
July 17, 2024Medical DevicesFDA
American Contract Systems Inc recalls FOOT ANKLE-LF Procedure tray Catalog Number:CCFA51B
Hazard: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding component exceeded the residual limits for permanent exposure devices as indicated by ANSI/AAMI/ISO 10993-7/(R)2012.