American Contract Systems Inc recalls
Every recall we track for American Contract Systems Inc — 198 in all, from 2018–2026 — plus the complaints and injury reports the public filed about them. 1 is rated “stop using now”.
Recalls per year, by danger level
Recalls from American Contract Systems Inc peaked in 2024 (66); 198 since 2017. 1% rated “stop using now”.
All FDA recall records for American Contract Systems Inc since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 1 | 0 | 1 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 1 | 1 | 15 | 9 | 26 |
| 2023 | 0 | 0 | 31 | 0 | 31 |
| 2024 | 0 | 0 | 61 | 5 | 66 |
| 2025 | 0 | 0 | 55 | 9 | 64 |
| 2026 (to date) | 0 | 2 | 6 | 2 | 10 |
Most common reasons for American Contract Systems Inc recalls
What to do if you have a recalled American Contract Systems Inc product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All American Contract Systems Inc recalls
22 shown- Use cautionMedical device
American Contract Systems Inc recalls Medical convenience kits containing BD CliniClean Pericare Wipes within BD Urinary Catheter Trays ABDOMINAL
American Contract Systems recalls 1,804 medical convenience kits containing BD CliniClean Pericare Wipes that may be contaminated with manufacturing lubricant, increasing risk of skin irritation or infection.
American Contract SystemsAug 10, 2026 - Lower riskMedical device
American Contract Systems Inc recalls American Contract System Convenience Kit, CV B PACK, Model/Catalog Number: TNCB10AN
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 SystemsJun 29, 2026 - Lower riskMedical device
American Contract Systems Inc recalls American Contract Systems medical procedure kits and trays labeled as: 1) CRANI PACK - 208400, Model Item Number
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 SystemsMay 19, 2026 - Use cautionMedical device
American Contract Systems Inc recalls Convenience kits containing Medline Namic Angiographic Control Syringes with Rotating Adaptor CORONARY ANGIO PACK Model
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 SystemsMar 19, 2026 - UnratedMedical device
American Contract Systems Inc. recalls Medical convenience kits Item Number/Description HSAN63N ANGIO PACK IHAN02W ANGIOGRAPHY PACK MHCA98AK CORONARY ANGIO
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 SystemsSep 4, 2025 - Lower riskMedical device
American Contract Systems Inc recalls AMERICAN CONTRACT SYSTEMS, Medical Procedure kits and trays labeled as: 1) ANTERIOR HIP PACK, MODEL/ITEM NUMBER
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 SystemsJul 14, 2025 - Lower riskMedical device
American Contract Systems, Inc. recalls LOWER EXTREMITY, Model: NCEX20I; LOWER EXTREMITY, Model: NCEX20J; TOTAL KNEE PACK, Model: NCTK31K; TOTAL KNEE PACK,
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 SystemsApr 21, 2025 - Lower riskMedical device
American Contract Systems Inc recalls MAJOR VASCULAR PACK , Model No UTMV78X-01 UTMV78Y UTMV78Y-01 UTMV78X-01 UTMV78Y-02
American Contract Systems recalls vascular packs with model numbers UTMV78X-01, UTMV78Y, etc. due to possible sterilization issues that could delay or prolong medical treatment.
American Contract SystemsFeb 6, 2025 - Lower riskMedical device
American Contract Systems Inc recalls CRANI PACK, Model/Catalog Number WECR41D, medical procedure kit.
American Contract Systems recalls CRANI PACK medical kits with model WECR41D due to potential failure in sterilization, risking infection during surgery. Affected kits have specific lot codes and expiration dates.
American Contract SystemsFeb 4, 2025 - Lower riskMedical device
American Contract Systems, Inc. recalls Brand Name: Banner University Med Ctr. Product Name: Cardiac Cath Lab Pack-170278 Model/Catalog Number: GSCC40G
Banner University Med Ctr recalls Cardiac Cath Lab Pack-170278 (GSCC40G) due to potential sterility issues with procedure trays. Affected units may not meet sterility standards for medical procedures.
Banner University Med CtrJan 31, 2025 - Lower riskMedical device
American Contract Systems, Inc. recalls Pacemaker, COPM11B; Medical convenience kit
American Contract Systems recalls Pacemaker COPM11B medical kits due to humidity readings causing sterilization concerns. Affected units have specific lot and expiration dates.
American Contract SystemsAug 7, 2024 - Lower riskMedical device
American Contract Systems Inc recalls TOTAL KNEE - 302497- Procedure tray Catalog Number: ANTK12AF
American Contract Systems recalls TOTAL KNEE Procedure Tray (Catalog ANTK12AF) due to excessive ethylene oxide/ethylene chlorohydrin residuals in cast padding, potentially causing tissue damage with prolonged use.
American Contract SystemsMay 15, 2024 - Lower riskMedical device
American Contract Systems, Inc. recalls American Contract Systems Spine Pack convenience kit
Recalled American Contract Systems Spine Pack convenience kits may not sterilize properly due to insufficient aeration time, risking contamination. Affected kits have specific UDI-DI and lot numbers.
American Contract SystemsMay 6, 2024 - Lower riskMedical device
American Contract Systems, Inc. recalls Procedural convenience kits and trays, cardiac, labeled as: a) EP LAB BI V IMPLANT PACK, kit number AGBI64J; b) LAB
American Contract Systems recalls cardiac procedural kits and trays with specific kit numbers and lot dates due to possible component failure from improper sterilization processes.
American Contract SystemsNov 29, 2023 - Lower riskMedical device
American Contract Systems, Inc. recalls LAVH, REF BBLV21C
American Contract Systems recalls LAVH and REF BBLV21C devices due to potential reduced drug efficacy from improper sterilization. Affected units have specific lot numbers and UDI/DI codes.
American Contract SystemsSep 1, 2023 - Lower riskMedical device
American Contract Systems, Inc. recalls Total Knee Pack, REF CETJ130, medical convenience kits
American Contract Systems recalls Total Knee Pack REF CETJ130 medical kits due to incorrect expiration dates. Affected units may expire prematurely, causing safety risks.
American Contract SystemsApr 17, 2023 - Lower riskMedical device
American Contract Systems, Inc. recalls BASIN SET, MEBS42K, general surgical kit
American Contract Systems recalls BASIN SET MEBS42K surgical kits due to labeling error where contents don't match package label. Affected units have specific batch numbers and expiration dates.
American Contract SystemsOct 12, 2022 - Use cautionMedical device
American Contract Systems, Inc. recalls COVID Test Kit Nonsterile
Recall of American Contract Systems' nonsterile COVID test kits with incorrect labeling for SARS-Co-V2 use. Do not use these kits with any SARS-Co-V2 testing devices.
American Contract SystemsAug 12, 2022 - Lower riskMedical device
American Contract Systems, Inc. recalls Various Angiography packs/trays
Recall of angiography packs/trays due to potential exposure to multiple sterilization cycles without validation. Affected items have specific tray numbers and lot codes.
American Contract SystemsJun 16, 2022 - Lower riskMedical device
American Contract Systems, Inc. recalls Clean Catch Urine Kit NS 178489, AHMU58A
American Contract Systems recalls Clean Catch Urine Kit NS 178489, AHMU58A due to potential improper assembly by untrained individuals. Affected lots include 891211, 737211, 699211, 986221.
American Contract SystemsMay 2, 2022 - Lower riskMedical device
American Contract Systems, Inc. recalls ACS Cath Lab Pack
American Contract Systems recalls ACS Cath Lab Pack model FTCL83K with lot 982221 for higher than specified EO sterilization concentration. This may cause equipment failure. Contact for details.
American Contract SystemsMar 22, 2022 - Lower riskMedical device
American Contract Systems, Inc. recalls Bag size #4 Custom Convenience Kits Usage: Surgical convenience kits labeled as the following: a. Tray Name: PACK BASIC
American Contract Systems recalls Bag size #4 Custom Convenience Kits used in surgery that may not have reached complete sterilization. Affected kits include specific tray names and lot numbers.
American Contract SystemsNov 21, 2018
American Contract Systems Inc recall questions
How many recalls has American Contract Systems Inc had?
198 recalls from American Contract Systems Inc are on record with U.S. safety agencies, from 2018–2026.
What is the most recent American Contract Systems Inc recall?
American Contract Systems Inc recalls Medical convenience kits containing BD CliniClean Pericare Wipes within BD Urinary Catheter Trays ABDOMINAL, dated Aug 10, 2026. Every American Contract Systems Inc recall is listed on this page, newest first.
Why are American Contract Systems Inc products recalled?
The most common reasons on record: Product was sterilized with a higher than specification EO concentration. (5); Sterility assurance with procedure trays (3).
What should I do if I have a recalled American Contract Systems Inc product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new American Contract Systems Inc recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.