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 50 entries, severity tagging shows 0 critical, 50 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 50 of 50 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 (50). The date window on this page runs from Nov 1, 2023 to Jul 17, 2024.

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 Jul 17, 2024

KNEE ARTHROSCOPY-Procedure Kit Catalog Number: QPKA35A

FDA Devices Moderate Jul 17, 2024

TOTAL KNEE - 247546 Procedure tray Catalog Number: BFTK01Z

FDA Devices Moderate Jul 17, 2024

HAND DRAPING SJH-Procedure Kit Catalog Number: SJHD67F

FDA Devices Moderate Jul 17, 2024

KNEE SCOPE Procedure tray Catalog Number: COKN48L

FDA Devices Moderate Jul 17, 2024

TOTAL KNEE -Procedure Kit Catalog Number: QPTK95A

FDA Devices Moderate Jul 17, 2024

TOTAL KNEE, ST LUKES Catalog Number: LMTK17AP

FDA Devices Moderate Jul 17, 2024

ARTHRO KNEE BEACHES PACK BHS- Procedure tray Catalog Number: BPKB46B

FDA Devices Moderate Jul 17, 2024

HAND WRIST FOREARM-LF Procedure tray Catalog Number: CCHD17B

FDA Devices Moderate Jul 17, 2024

AHAR50K STANDARD ARTHROSCOPY PACK - 291852. Procedure tray Catalog Number: AHAR50K

FDA Devices Moderate Jul 17, 2024

TOTAL KNEE - 247546 - Procedure tray Catalog Number: BFTK01AA

FDA Devices Moderate Jul 17, 2024

CUSTOM KNEE - 206061-Procedure Kit Catalog Number: UDKN68AG

FDA Devices Moderate Jul 17, 2024

TOTAL KNEE -Procedure Kit Catalog Number: QPTK95B

FDA Devices Moderate Jul 17, 2024

TOTAL KNEE - 297835 -Procedure Kit Catalog Number: RGTK10L

FDA Devices Moderate Jul 17, 2024

BPKN15C KNEE BASIN PACK BHS- Procedure tray Catalog Number: BPKN15C

FDA Devices Moderate Jul 17, 2024

ARTHROSCOPY PACK-Procedure Kit Catalog Number: TNAR22U

FDA Devices Moderate Jul 17, 2024

ARTHO KNEE BAPTIST SOUTH PACK Procedure tray Catalog Number: BPKA49B

FDA Devices Moderate Jul 17, 2024

ACL PACK - 206039-Procedure Kit Catalog Number: UDAC66AA

FDA Devices Moderate Jul 17, 2024

TOTAL KNEE-Procedure Kit Catalog Number: SMTK21C

FDA Devices Moderate Jul 17, 2024

KNEE ARTHROSCOPY PACK Catalog Number: MEKA12R

FDA Devices Moderate Jul 17, 2024

MAJOR KNEE - 302497- Procedure tray Catalog Number: ASKN23B

FDA Devices Moderate Jul 17, 2024

ORIF HIP - IM RODDING FEMUR-Procedure Kit Catalog Number: UTHP44S

FDA Devices Moderate Jul 17, 2024

CUSTOM KNEE - 206061-Procedure Kit Catalog Number: UDKN68AE

FDA Devices Moderate Jul 17, 2024

TOTAL KNEE - 297835-Procedure Kit Catalog Number: RGTK10K

FDA Devices Moderate Jul 17, 2024

FOOT ANKLE-LF Procedure tray Catalog Number:CCFA51B

FDA Devices Moderate Jul 17, 2024

TOTAL KNEE-Procedure Kit Catalog Number: SFTK54B

FDA Devices Moderate Jul 17, 2024

LOWER EXTREMITY - 247542- Procedure tray Catalog Number: BFLE56X

FDA Devices Moderate Jul 17, 2024

ARTHROSCOPY PACK-Procedure Kit Catalog Number: TNAR22V

FDA Devices Moderate Jul 17, 2024

KNEE ARTHROSCOPY PACK-Procedure Kit Catalog Number: WEKA15B

FDA Devices Moderate Jul 17, 2024

ACL, ST LUKES METHODIST 1CS Catalog Number: LMAC10AA

FDA Devices Moderate Jul 17, 2024

HAND PACK 297829--Procedure Kit Catalog Number: RGHN04I

FDA Devices Moderate Jul 17, 2024

KNEE ARTHROSCOPY PACK-Procedure Kit Catalog Number: SFAR60A

FDA Devices Moderate Feb 7, 2024

Procedural convenience kits and trays, cardiac, labeled as: a) EP LAB BI V IMPLANT PACK, kit number AGBI64J; b) LAB DEVICE IMPLANT, kit number A…

FDA Devices Moderate Feb 7, 2024

Custom procedural convenience kits and trays, ear, nose & throat, labeled as: a) T AND A PACK AGH ASC, kit number AGTA48J; b) OPSC EAR PACK, kit…

FDA Devices Moderate Feb 7, 2024

Custom procedural convenience kits and trays, Obstetrical & Gynecological use, labeled as: a) LavH, kit number BBLV21C; b) LAP HYST 247540, ki…

FDA Devices Moderate Feb 7, 2024

Custom procedural convenience kits and trays, cardiac, labeled as: a) CENTRAL LINE INSERTION PACK, kit number LLCE52; b) Adult Central Line Inse…

FDA Devices Moderate Feb 7, 2024

Custom procedural convenience kits and trays, general & plastic surgery, labeled as: a) BRACHY THERAPY PROCEDURE PAC, kit number AGBR90E; b) BRA…

FDA Devices Moderate Feb 7, 2024

Custom procedural convenience kits and trays, gastroenterological & urological, labeled as: a) LAP KIDNEY MODULE, kit number AGKD50L; b) ROBOTIC…

FDA Devices Moderate Feb 7, 2024

Custom procedural convenience kits and trays, general hospital use, labeled as: a) Baby PICC Kit, kit number UIBP90J; b) Baby PICC Kit, kit numb…

FDA Devices Moderate Feb 7, 2024

Custom procedural convenience kits and trays, Obstetrical & Gynecological use, labeled as: a) LOWER PELVIC PACK, kit number AGLP52L; b) OB/GYN D…

FDA Devices Moderate Feb 7, 2024

Custom procedural convenience kits and trays, Obstetrical & Gynecological use, labeled as: a) C-SECTION PACK, kit number FDCS01AA; b) C-SECTION …

FDA Devices Moderate Feb 7, 2024

Custom procedural convenience kits and trays, cardiac, labeled as: a) HEART CATHETERIZATION TRAY, kit number JRHC45G; b) TAVR PACK, kit number L…

FDA Devices Moderate Feb 7, 2024

Custom procedural convenience kits and trays, general hospital use, labeled as: a) IR NEURO PACK, kit number AGNE20J; b) ADULT CRANIOTOMY PACK, …

FDA Devices Moderate Feb 7, 2024

Custom procedural convenience kits and trays, gastroenterological & urological, labeled as: AHN BIOPSY STERILE, kit number AHBP12A

FDA Devices Moderate Feb 7, 2024

Custom procedural convenience kits and trays, general & plastic surgery, labeled as: a) Breast Plastics Pack, kit number BBPL20D; b) MINOR PLAST…

FDA Devices Moderate Feb 7, 2024

Custom procedural convenience kits and trays, Obstetrical & Gynecological use, labeled as: a) LABOR & DELIVERY PACK, kit number HILD52F; b) LABO…

FDA Devices Moderate Feb 7, 2024

Custom procedural convenience kits and trays, urological, labeled as: a) UROLOGY DAVINCI PACK, kit number HGUR87G; b) CYSTO PACK, kit number LVC…

FDA Devices Moderate Feb 7, 2024

Custom procedural convenience kits and trays, anesthesia, labeled as: a) HEART ANESTHESIA BUNDLE NS, Kit Number LMHA01V; b) OR/Anesthesia Centra…

FDA Devices Moderate Feb 7, 2024

Custom procedural convenience kits and trays, Ophthalmic use, labeled as: a) EYE PACK, kit number LVEY27; b) Laminectomy, kit number UIOL34AG

FDA Devices Moderate Feb 7, 2024

Custom procedural convenience kits and trays, Othopedic use, labeled as: a) HIP FRACTURE, kit number AHHF15C; b) HIP FRACTURE, kit number AHHF15…

FDA Devices Moderate Nov 1, 2023

LAVH, REF BBLV21C

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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.