Every recall we track for American Contract Systems Inc — 195 in all — plus the complaints and injury reports the public filed about them.
American Contract Systems recalls Convenience Kits CV B PACK (TNCB10AP) due to catheters not meeting performance specs. Affected units sold until Jan 2027.
American Contract Systems recalls Convenience Kit CV B PACK (TNCB10AM) due to catheters not meeting performance specs. Affected units sold through specific channels until 7/15/2026.
American Contract Systems recalls Convenience Kit CV B PACK (Model TNCB10AN) due to catheters not meeting performance specs. Affected units sold until Jan 2027.
American Contract Systems recalls Convenience Kit D & C PACK (LLPD90H) due to catheters not meeting performance specs. Affected units sold with lot code 70-054952.
Recall of specific medical procedure kits due to potential for unexpected endotoxin levels in Ritmed Neurological Sponges. Affected items include CRANI PACK, SPINE PACK, and other surgical trays with listed model numbers and lot numbers.
American Contract Systems recalls specific medical procedure kits due to potential endotoxin level variations in Ritmed Neurological Sponges, which could affect surgical safety.
American Contract Systems recalls convenience kits with Medline Namic Angiographic Control Syringes that may disconnect during use, risking blood exposure, infection, or air embolism. Affected kits have specific model numbers and lots.
American Contract Systems recalls medical convenience kits that may have been re-gassed more than once during sterilization, risking product safety and effectiveness. Affected kits include specific item numbers and serial numbers.
American Contract Systems recalls adult central line insertion supply kits that were re-gassed after initial sterilization, risking product safety and effectiveness.
American Contract Systems recalls medical convenience kits that were re-gassed more than once during sterilization, risking product safety and effectiveness. Affected kits may not be safe for use.
American Contract Systems recalls medical convenience kits that were re-gassed more than once during sterilization. Products may not be safe or effective due to unvalidated multiple sterilization cycles.
American Contract Systems recalls medical convenience kits that were re-gassed more than once during sterilization, risking product safety and effectiveness. Affected kits include Heart Pack, CV Set Up Pack, and Pacemaker Pack models.
American Contract Systems recalls medical convenience kits that were re-gassed (sterilized more than once) after a nonconformance during initial sterilization. Products may not be safe or effective due to unvalidated multiple sterilization cycles.
American Contract Systems recalls medical convenience kits that may have been re-gassed more than once during sterilization, risking product safety and effectiveness. Consumers should check item numbers and serial numbers for affected units.
American Contract Systems recalls medical convenience kits that were re-gassed (sterilized more than once) after initial Ethylene Oxide process. Product quality, safety, and effectiveness cannot be confirmed due to unvalidated multiple sterilization cycles.
American Contract Systems recalls LKRA40G RADIOLOGY PACK medical kits that may have been re-gassed more than once during sterilization, risking product safety and effectiveness.
American Contract Systems recalls UDPG88W PICC G-TUBE PACK kits that were re-gassed after initial sterilization, risking product safety and effectiveness.
American Contract Systems recalls Basic Biopsy Trays that were re-gassed after initial sterilization. These products may not be safe or effective due to multiple sterilization cycles.
American Contract Systems recalls medical convenience kits that were re-gassed (sterilized more than once) after a nonconformance during initial sterilization. These products may not be safe or effective due to unvalidated multiple sterilization cycles.
American Contract Systems recalls Basic Biopsy Tray (NMBP44L) due to potential re-gassing during sterilization, risking product safety and effectiveness.
American Contract Systems recalls IHDC30R medical convenience kits that were re-gassed more than once during sterilization, risking product safety and effectiveness.
American Contract Systems recalls medical delivery kits that were re-gassed after initial sterilization, risking product safety and effectiveness. Affected kits may not be safe for use due to multiple sterilization cycles.
American Contract Systems recalls medical cysto packs that were re-gassed more than once during sterilization, risking product safety and effectiveness.
American Contract Systems recalls medical convenience kits that may have been re-gassed more than once during sterilization, risking product safety and effectiveness. Consumers should check item numbers and lot numbers for affected kits.
American Contract Systems recalls medical convenience kits that may have been re-gassed more than once during sterilization, risking product safety and effectiveness.
American Contract Systems recalls medical procedure kits with model GRRB10E and SPVH62P due to unverified sterilization. Affected kits may not meet safety standards.
American Contract Systems recalls medical procedure kits and trays due to unverified sterilization. Products labeled CYSTO with specific model numbers and lot numbers may not meet sterilization standards.
American Contract Systems recalls laparoscopy and pelviscopy kits with model numbers EVLP61I and EVPV29G due to unverified sterilization. Products may not meet safety standards after use.
American Contract Systems recalls medical procedure kits with model numbers CILC69L, HNLC80J, JKLC55H, LLLA21K, and MPGL15G due to unverified sterilization status. Products may not be safe for use after sterilization.
American Contract Systems recalls 16 medical procedure kits due to unverified sterilization of components. Products may not meet sterilization standards, posing potential infection risks. Affected kits include A-C Supplement Pack, Kidney Perfusion Pack, and others.
American Contract Systems recalls 27 medical procedure kits due to unverified sterilization. Products may not meet sterilization standards, but no injuries reported. Check model numbers and lot numbers for affected items.
American Contract Systems recalls medical procedure kits with unverified sterilization. Some components may not be sterilized properly, risking infection. Affected kits have specific model numbers and lot codes.
American Contract Systems recalls medical procedure kits with unverified sterilization. Some components may not be safe for reuse after sterilization. Affected kits include BORN ON ARRIVAL KIT (LLBN11C) and LABOR & DELIVERY PACK (LLLD19I).
American Contract Systems recalls 7 medical procedure kits due to unverified sterilization status. Some components may not meet sterilization standards, risking infection during surgery.
American Contract Systems recalls specific cast padding kits due to ethylene oxide/ethylene chlorohydrin residuals exceeding safety limits, potentially causing treatment delays or complications.
American Contract Systems recalls Total Hip Pack models SMTH06O and SMTH06P due to possible sterilization issues causing treatment delays. Affected units sold between 2005-2:05 and 2005-05.
American Contract Systems recalls LAPAROSCOPY PACK models CALS41F and CALS41G due to possible failure in sterilization assurance, which may cause treatment delays or prolonged procedures.
American Contract Systems recalls LAPAROSCOPY PACK models LLLA21J and LLLA21J-02 due to possible sterilization issues affecting medical use safety.
American Contract Systems recalls EAR PACK Model SFEA12A due to possible sterilization issues causing treatment delays. Affected units have specific lot numbers and were sold in the U.S. Learn what to do.
American Contract Systems recalls laceration trays with model numbers SGLA07A, SGLA07B-0: possible sterilization failure may delay or prolong treatment. No remedy specified in recall notice.
American Contract Systems recalls NEURO IR TRAY Model WENI56J due to possible failure in sterilization, risking treatment delays. Affected units have specific lot numbers and UDI-DI codes.
American Contract Systems recalls SPINE LUMBAR PACK models UTSL72AA/UTSL7: Possible treatment delays due to unconfirmed sterilization. Affected units sold with specific lot numbers.
American Contract Systems recalls MAJOR DIEP models CCMJ73G-01 and CCMJ7: Possible treatment delays due to unconfirmed sterilization. Return or stop use to avoid risks.
American Contract Systems recalls CV BASIC PUMP PACK Model WECV23D due to possible sterilization issues affecting treatment safety. Affected units sold with specific lot numbers.
American Contract Systems recalls OPEN HEART A PACK models UTOH19AI, UTOH19AJ-01, UTOH19AJ-02 due to possible failure in sterilization assurance, which could delay or prolong medical treatment.
American Contract Systems recalls thoracic packs with model UTTC82Y/UTTC82AA-01 due to potential sterilization issues causing treatment delays. Affected units sold from specific lots.
American Contract Systems recalls AV FISTULA Model UTAV77T due to unconfirmed sterilization. This may cause treatment delays or reduced functionality. Check product details for affected units.
American Contract Systems recalls C-SECTION PPS models LLCI66M-02 to -04 due to possible sterilization issues causing treatment delays. No remedy provided in official notice.
American Contract Systems recalls General Angio Packs with specific model numbers due to unconfirmed sterilization. This may cause treatment delays or prolonged procedures. Affected units include model LLAP75G and variants.
American Contract Systems recalls URO ROBOTIC PACK models LVUR44C and LVUR44C-03 due to possible sterilization issues causing treatment delays. Affected units sold from 2022-2023.
American Contract Systems recalls BORN ON ARRIVAL Kit (Model LLBN11B) due to unconfirmed sterilization. This may cause treatment delays or reduced functionality. Affected units sold with specific lot numbers.
American Contract Systems recalls CYSTO PACK Model N HKCY31A due to possible sterilization issues causing treatment delays. Affected units have specific lot numbers and UDI-DI codes.
American Contract Systems recalls VEIN TRAY models UTVT21C and variants due to possible sterilization issues affecting treatment safety. Affected units may cause delays or complications in medical procedures.
American Contract Systems recalls LABOR & DELIVERY PPS models LLLD64O-01, -02 due to possible sterilization issues affecting medical use. No remedy specified in recall notice.
American Contract Systems recalls DR DIULUS injection packs with model numbers CCDU12C, CCDU12D, and CCDU12D-01 due to possible failure in sterilization assurance, which may cause treatment delays or complications.
American Contract Systems recalls CYSTO Model SACY80: Unconfirmed sterilization may cause treatment delays or malfunction. Affected units have specific lot numbers.
American Contract Systems recalls LAPAROSCOPY PACK models SFLA02A/B due to possible sterilization failure risking treatment delays. Affected units sold from 2005-2007.
American Contract Systems recalls laceration trays with model numbers SGLA07A, SGLA07B-0: possible sterilization failure may delay or prolong medical treatment. No remedy specified.
American Contract Systems recalls HIP SCOPE models CCHS21B and variants due to unconfirmed sterilization. This may cause treatment delays or reduced functionality. Affected units sold with specific serial numbers.
American Contract Systems recalls OPEN HEART Adult Side A devices with specific model numbers due to potential sterilization issues that could cause treatment delays.
