PlainRecalls

American Contract Systems, Inc.

Compiled from official public sources by the editorial team.

190 recalls on record · Latest: May 13, 2026

American Contract Systems, Inc. Recall Insight

American Contract Systems, Inc. appears on 190 federal recall records indexed by PlainRecalls, out of 101,704 total recalls tracked across the FDA, CPSC, and NHTSA. That represents approximately 0.187% of the federal archive, a data point that is only interpretable alongside production volume, product mix, and decades of operation, because a high recall count alone does not establish fault. Large, diversified firms that sell tens of millions of units across many categories will mechanically accumulate more recall records than small manufacturers, even when their defect rates per unit shipped are comparable or lower. The most recent action on this firm is dated May 13, 2026, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 40 entries, severity tagging shows 2 critical, 37 moderate, and 1 lower-severity recalls. Affected-unit counts are disclosed on 40 of 40 entries, unit-count disclosure is more common on CPSC and NHTSA actions and less common on FDA drug/device recalls, where lot numbers and distribution scope substitute for absolute totals. The records on this page span 1 distinct product categories, with issuing agencies dominated by FDA Devices (40). The date window on this page runs from Nov 21, 2018 to Nov 1, 2023.

Manufacturer-level browsing is useful when monitoring a single firm for patterns, whether recalls cluster around one product family (suggesting a specific design or supplier issue) or scatter across the firm's entire catalog (which can indicate systemic quality-control problems or deliberate regulator attention). Clicking into each recall reveals the specific hazard, remedy, and distribution scope that together determine whether a consumer is actually at risk. For decisions that depend on being current, deciding whether a product in your home is safe, whether to return a gift, or whether to accept a replacement, always verify the recall number on the issuing agency's site, because federal agencies amend, terminate, and re-scope recalls over time and only the agency's live record reflects the current legal status. This page aggregates what agencies have published publicly and is intended for consumer awareness and research.

FDA Devices Moderate Nov 1, 2023

Robotics Pack SAH, REF SAR530M

FDA Devices Moderate Nov 1, 2023

Robotics Pack, REF SJVO56B

FDA Devices Moderate Nov 1, 2023

Vasc. Open CVOR SJH, REF SJVO56B

FDA Devices Moderate Nov 1, 2023

CVS PCSU SJH, REF SJCV48J

FDA Devices Moderate Nov 1, 2023

Pediatric Heart SJH, REF SJPH34K

FDA Devices Moderate Nov 1, 2023

Cath Cardiac Pack, REF IHCC03V

FDA Devices Moderate Nov 1, 2023

Robotics Pack, REF SSRO22D

FDA Devices Moderate Nov 1, 2023

Sub Q Recorder Pack, REF BPRC87A

FDA Devices Moderate Nov 1, 2023

Breast Plastics Pack, REF BBPL20D

FDA Devices Moderate Nov 1, 2023

Pediatric Urology Wolson Pack, REF BPPU55A

FDA Devices Moderate Nov 1, 2023

General Pack, REF BBGP31C

FDA Devices Low Jun 21, 2023

Total Knee Pack, REF CETJ130, medical convenience kits

FDA Devices Moderate Nov 30, 2022

BASIN SET, MEBS42K, general surgical kit

FDA Devices Moderate Oct 19, 2022

COVID Test Kit Nonsterile

FDA Devices Moderate Sep 14, 2022

Various Angiography packs/trays

FDA Devices Moderate Sep 14, 2022

Breast Abdominoplasty Pack

FDA Devices Moderate Sep 14, 2022

Various C-section packs

FDA Devices Moderate Sep 14, 2022

Various convenience packs

FDA Devices Moderate Sep 14, 2022

Various convenience packs

FDA Devices Moderate Sep 14, 2022

D&C pack

FDA Devices Moderate Sep 14, 2022

Various Port Insertion Packs

FDA Devices Moderate Sep 14, 2022

Various ob/gyn packs

FDA Devices Moderate Sep 14, 2022

Various eye packs, cataract packs

FDA Devices Moderate Sep 14, 2022

Various neurology packs

FDA Devices Moderate Sep 14, 2022

Various Pacemaker Packs, Cardio Thoracic Packs

FDA Devices Moderate Sep 14, 2022

Various ENT Packs

FDA Devices Moderate Sep 14, 2022

Various Angiography/Cath Lab packs/trays

FDA Devices Moderate Sep 14, 2022

Various Cysto Packs

FDA Devices Moderate Sep 14, 2022

Various hysterectomy, vaginal packs

FDA Devices Moderate Sep 14, 2022

Various Laparoscopy Packs

FDA Devices Moderate Sep 14, 2022

Various PICC Line, Central Line Packs

FDA Devices Critical Jul 13, 2022

Clean Catch Urine Kit NS 178489, AHMU58A

FDA Devices Critical Jul 13, 2022

Nasopharyngeal sample collection tray for COVID-19 testing, labeled as COVID TEST KIT NONSTERILE 184312, AHCV18A

FDA Devices Moderate May 18, 2022

ACS Cath Lab Pack

FDA Devices Moderate May 18, 2022

ACS Lap Chole Pack

FDA Devices Moderate May 18, 2022

1) ACS Spine Pack 2) ACS Lumbar/Back Set Up Tray

FDA Devices Moderate May 18, 2022

1) ACS Arthroscopy Kit 2) ACS Knee Kit 3) ACS Hand Pack

FDA Devices Moderate May 18, 2022

ACS IR - Angio Pack

FDA Devices Moderate Mar 6, 2019

Bag size #4 Custom Convenience Kits Usage: Surgical convenience kits labeled as the following: a. Tray Name: PACK BASIC SET UP LH - 203510…

FDA Devices Moderate Nov 21, 2018

Powdered Surgical Gloves, labeled as: a. Baxter and Ansell brand Powdered Surgical Gloves b. Powdered Surgical Gloves included in ACS surgical co…

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Data Sources

  • Source: FDA + CPSC + NHTSA - federal recall filings naming this firm. Verify with FDA, CPSC, or NHTSA directly.
  • Source: PlainRecalls Manufacturer Index - firm-level aggregation across all three federal recall feeds

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Recalls are aggregated across FDA, CPSC and NHTSA filings that name this firm; the total reflects the federal record, not an independent investigation. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.