American Contract Systems Inc
190 recalls on record · Latest: May 13, 2026
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Agency notice ledger
Federal filing book American Contract Systems I… HEAVY-BOOK · SINGLE-AGENCY
#81 of 14,151 · 190 notices · 0.182% archive
- BOOK 190 notices
- RANK #81 of 14,151
- SHARE 0.182% archive
- AGENCY FDA Devices (190)
- CAT medical devices
- CATS 1 category
- LATEST May 13, 2026
- PHOTO High Liner Foods Inc.
Nearest notice-volume peer: High Liner Foods Inc. (1 notice gap)
American Contract Systems Inc accounts for about 0.182% of the 104,423-notice archive on 190 distinct filings — a heavy share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →
American Contract Systems I…'s standing among 14,151 recalling firms
American Contract Systems Inc ranks 81st of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.
American Contract Systems I… vs all firms by recall-notice count
Where this firm's archive sits among every tracked recalling manufacturer
190 81st of 14151 higher than 14,070 of 14,151 firms
Firms, banded by distinct federal recall-event inventory
Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-09-13
American Contract Systems I… in the notice-volume neighbourhood
Distinct federal recall events among this firm and nearest nationwide peers
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194 notices
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194 notices
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192 notices
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High Liner Foods Inc.
191 notices
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American Contract Systems Inc
190 notices
- Chevrolet,Gmc
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188 notices
What this shows American Contract Systems Inc holds about 0.182% of archive notices alongside 190 distinct filings.
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 AGDI40J; c) LAB DEVICE IMPLANT, kit number AGDI40K; d) MINOR VASCULAR, kit number AGMV26O; e) OPEN HEART ACCESSORY, kit number AGOH98Q; f) OPEN HEART ACCESSORY, kit number AGOH98R; g) OPEN HEART ACCESSORY, kit number AGOH98S; h) PERIPHERAL VASCULAR, kit number AGPV28O; i) PERIPHERAL VASCULAR, kit number AGPV28P; j) MINOR VASCULAR, kit
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 number LLEO66; c) T AND A PACK, kit number MMTA41F
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, kit number BFHY75U
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 Insertion Supply Kit, kit number UICL44N; c) Pediatric Central Line Insertion, kit number UIPL77K
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) BRACHY THERAPY PROCEDURE PAC, kit number AGBR90E; c) MINI MINOR AGH ASC PACK, kit number AGMM60M; d) OUTPATIENT PORT ACCESS KIT 307907, kit number AHPO55J; e) General Pack, kit number BBGP31C; f) FRACTURE TABLE PACK, kit number FDFT75N; g) Arthroscopy Pack, kit number HCAR04K; h) BARIATRIC PACK, kit number HGBA92F; i) LAPAROTOMY PACK, ki
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 PROSTATE PACK - 264852, kit number ANPR34S; c) LAP CHOLE - 213388, kit number BFLC02AD; d) GENERAL LAPAROSCOPY PACK, kit number GUGE09I; e) LAP CHOLE PACK, kit number HNLC80I; f) Lap Chole Ovarian Appy, kit number JSLC06I; g) LAP CHOLE, ST LUKES, kit number LMLP08Z; h) ROBOTIC PACK - 242561, kit number MHRB88AJ; i) KIT, GENERAL LAPARO
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 number UIBP90K; c) PORT PACK (PS 058330), kit number UIPO82AB; d) Pediatric PICC Kit, kit number UIPP76K;
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 DAVINCI PACK A RG BASIN, kit number HGOB98G; c) DAVINCI GYN PACK, kit number HHDV17; d) KIT, GYNE ROBOTIC, kit number MMGR44D; e) KIT, MAJOR LITHOTOMY, kit number MMJL16E; f) GYN PACK, kit number SMGY46; g) Lithotomy Pack, kit number THLH71C; h) ASC HYSTEROSCOPY PACK (PS 020634), kit number UIHY16AA; i) GYN LAPAROSCOPY HPES, kit number
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 PACK, kit number FDCS01AB; c) C-SECTION STERILE PACK, kit number HGCS68J; d) C-SECTION PACK, kit number HICS50H; e) C-SECTION PPS, kit number LLCI66; f) C-Section drape Pack, kit number RBCS12R; g) C-Section, kit number THCS49B; h) C-SECTION PACK (PS 020632), kit number UICS50AG;
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 LLTV10; c) CATH PED LF SJH, kit number SJCA21F; d) CATH HEART ADL LF SJH, kit number SJCH22F; e) INT RAD PORTS-LF - 206060, kit number UDIR58AL
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, kit number LLCR99; c) LAMINECTOMY PACK, kit number LLLC26; d) KIT, CRANIOTOMY, kit number MMCR11J; e) KIT, NEURO SPINE, kit number MMNS20H; f) IR NEURO PACK, kit number OSIN77; g) NEURO SAH, kit number SANE32H; h) NEURO SAH, kit number SANE32I; i) S78FCH CRANI PACK (PS 132432), kit number UICR10U; j) CRANI PACK (PS039498), kit number
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 PLASTIC, kit number WPMP16H
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) LABOR & DELIVERY PACK, kit number HILD52G
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 LVCY20; c) URO ROBOTIC PACK, kit number LVUR44;
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 Central Line Insertion Kit, Kit Number UIAN43L
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 AHHF15D; c) Hand Pack, kit number BBHP10E; d) Lower Extremity, kit number BBLE40B; e) Custom Podiatry, kit number BOCP70J; f) ROBOTIC PACK, kit number BPAR65A; g) HIP PINNING PACK, kit number EMHP84; h) HIP PINNING PK, STRL F G, kit number FHHI17V; i) TOTAL HIP PACK, kit number GNTH06L; j) TOTAL KNEE PACK, kit number GNTK07L; k) EXTREMIT
FDA Devices Moderate Nov 1, 2023
LAVH, REF BBLV21C
American Contract Systems I… carries an outsized archive share
Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.
Similar recall count
Nearest multi-notice firms by distinct-event totals (190 here — heavy-book).
Similar medical devices volume
Nearest multi-notice firms in the same narrow category lane.
Frequently Asked Questions
How many federal recall notices name American Contract Systems I…? ▼
PlainRecalls indexes 190 distinct federal recall events naming American Contract Systems Inc, aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of September 2026). That count is an issuance inventory, not a hazard score.
Where does American Contract Systems I… sit among other recalling firms? ▼
American Contract Systems Inc ranks #81 of 14,151 by distinct recall-event count among 14,151 firms in this archive (99th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of American Contract Systems I…'s notices? ▼
FDA Devices accounts for 190 of this firm's 190 indexed notices.
What product category dominates American Contract Systems I…'s filing book? ▼
Filings for American Contract Systems Inc span 1 product category, led by medical devices. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous? ▼
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
American Contract Systems Inc: 190 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Devices). Verify individual notices with FDA directly before acting on a specific recall.
Firm-level totals aggregate distinct federal recall events naming American Contract Systems Inc; individual notices remain authoritative on each linked recall page.
Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026