PlainRecalls

Cardinal Health 200, LLC

Compiled from official public sources by the publisher.

285 recalls on record · Latest: Aug 19, 2026

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Agency notice ledger

Federal filing book Cardinal Health 200, LLC HEAVY-BOOK · MULTI-AGENCY

#39 of 14,151 · 285 notices · 0.273% archive

  • BOOK 285 notices
  • RANK #39 of 14,151
  • SHARE 0.273% archive
  • AGENCY FDA Devices (284)
  • CAT medical devices
  • CATS 2 categories
  • LATEST Aug 19, 2026
  • PHOTO Reser's Fine Foods, I…

Nearest notice-volume peer: Reser's Fine Foods, Inc. (1 notice gap)

Cardinal Health 200, LLC accounts for about 0.273% of the 104,423-notice archive on 285 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 →

Cardinal Health 200, LLC's standing among 14,151 recalling firms

Cardinal Health 200, LLC ranks 39th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Cardinal Health 200, LLC vs all firms by recall-notice count

Where this firm's archive sits among every tracked recalling manufacturer

285 39th of 14151 higher than 14,112 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

Cardinal Health 200, LLC in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Cardinal Health 200, LLC holds about 0.273% of archive notices alongside 285 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026

How the 285 notices break down

Same federal filing book as the hero total — split by issuing agency, no new counts.

FDA Devices Moderate Sep 9, 2020

PROTEXIS Latex Micro Surgical Gloves Size 6.5 - Product Usage: This surgeon s glove is a disposable device made of natural rubber latex or synthetic rubber intended to be worn by operating room personnel to be a barrier protection from contamination. Various thickness for sensitivity or durability depending on need.
FDA Devices Moderate Jul 15, 2020

Cardinal Health NPWT Canister with Gel 300cc, Prescription Only - Product Usage: The systems are intended for use on patients with chronic, acute, traumatic, sub-acute and dehisced wounds, partial-thickness burns, ulcers (such as diabetic or pressure), flaps and grafts. The Cardinal Health NPWT PRO family of systems provides care in the acute, extended and home care settings.
FDA Devices Moderate Jul 15, 2020

Cardinal Health NPWT Occlusion Detection Canister 300cc, Prescription Only - Product Usage: The systems are intended for use on patients with chronic, acute, traumatic, sub-acute and dehisced wounds, partial-thickness burns, ulcers (such as diabetic or pressure), flaps and grafts. The Cardinal Health NPWT PRO family of systems provides care in the acute, extended and home care settings.
FDA Devices Moderate Mar 18, 2020

Monoject Hypodermic Safety Needle 30G X 1/2" Item Code 1183005 - Product Usage: used for general purpose injection and aspiration of fluids from vials, ampules and parts of the body below the surface of the skin.
FDA Devices Moderate Mar 18, 2020

Monoject 3mL Syringe with Hypodermic Safety Needle, 22G x 1-1/2 . Item Code 11832215 - Product Usage: used for general purpose injection and aspiration of fluids from vials, ampules and parts of the body below the surface of the skin.
FDA Devices Moderate Mar 18, 2020

Monoject Hypodermic Safety Needle 25G x 5/8" Item Code 1182558 - Product Usage: used for general purpose injection and aspiration of fluids from vials, ampules and parts of the body below the surface of the skin.
FDA Devices Moderate Mar 18, 2020

Monoject Bluntfill with Filter, 18G x 1-1/2" Item Code 11811022F. Used for drawing fluid from a vial - Product Usage: used for general purpose injection and aspiration of fluids from vials, ampules and parts of the body below the surface of the skin.
FDA Devices Moderate Feb 26, 2020

Presource Procedure Packs containing AAMI Level 3 surgical gowns, Multiple Catalog Numbers Produced Between September 1, 2018 and January 15, 2020. Additional kits produced through February 19, 2020 were included.
FDA Devices Moderate Feb 26, 2020

Presource Procedure Packs containing AAMI Level 3 surgical gowns, Multiple Catalog Numbers Produced Between September 1, 2018 and January 15, 2020
FDA Devices Moderate Feb 12, 2020

Genius 2 Tympanic Thermometer OEM Tympanic Item Code:303062
FDA Devices Moderate Feb 12, 2020

Genius 2 Tympanic Thermometer Private Label Item Code: 3069
FDA Devices Moderate Feb 12, 2020

Genius 2 Tympanic Thermometer (discontinued) Item Code: 303000
FDA Devices Moderate Feb 12, 2020

Genius 3 Tympanic Thermometer- electric thermometer Item Code: 303013
FDA Devices Moderate Feb 12, 2020

Genius 2 Tympanic Thermometer OEM Tympanic Item Code: 303063
FDA Devices Moderate Jul 31, 2019

Monoject Standard Hypodermic Needle, 20 G x 1-1/2" bulk Item code: 8881200664
FDA Devices Moderate Jul 31, 2019

Monoject Standard Hypodermic Needle, 27 G x 1-1/4" Item code: 8881200508
FDA Devices Moderate Jul 31, 2019

Monoject Standard Hypodermic Needle Item code: 8881200029
FDA Devices Moderate Jul 31, 2019

Monoject Standard Hypodermic Needle, 16 G x 1-1/2" Item code:8881200045
FDA Devices Moderate Jul 31, 2019

Monoject Blunt Cannula, 16 G x 1-1/2" (1.651 mm x 3.8 cm) Item code: 8881202322
FDA Devices Moderate Jul 31, 2019

Monoject Standard Hypodermic Needle, 14 G x 1-1/2" Item code: 8881200011
FDA Devices Moderate Jul 31, 2019

Monoject Blunt Cannula, 22 G x 1-1/2" (0.711 mm x 3.8 cm) Item code: 8881202389
FDA Devices Moderate Jul 31, 2019

Monoject 201 Vet Pak Hypodermic Needle, 19 ga x 1-1/2 Item code: 8881201522
FDA Devices Moderate Jul 31, 2019

Monoject 201 Vet Pak Hypodermic Needle, 22 ga x 1-1/2" Item code: 8881201456
FDA Devices Moderate Jul 31, 2019

Monoject 201 Vet Pak Hypodermic Needle, 20 ga x 1-1/2" Item code: 8881201498
FDA Devices Moderate Jul 31, 2019

Monoject Blunt Cannula, 15 G x 1-1/2" (1.829 mm x 3.8 cm) Item code: 8881202314
FDA Devices Moderate Jul 31, 2019

Monoject Blunt Cannula, 20 G x 1-1/2" (0.902 mm x 3.8 cm) Item code: 8881202363
FDA Devices Moderate Jul 31, 2019

Monoject 201 Vet Pak Hypodermic Needle, 18 ga x 1-1/2 Item code: 8881201548
FDA Devices Moderate Jul 31, 2019

Monoject Standard Hypodermic Needle, 18 G x 1-1/2" Item code: 8881200078
FDA Devices Moderate Jul 31, 2019

Monoject Standard Hypodermic Needle, 16 G x 1-1/2" Item code: 8881200037
FDA Devices Moderate Jul 31, 2019

Monoject" 201 Vet Pak Hypodermic Needle, 16 ga x 1-1/2 Item code: 8881201654
FDA Devices Moderate Jul 31, 2019

Monoject Blunt Cannula, 19 G x 1-1/2" (1.067 mm x 3.8 cm) Item code: 8881202355
FDA Devices Moderate May 15, 2019

ChemoPlus Chemo Spill Kit Product Code:CT4004 Product Usage: ChemoPlus chemotherapy spill kits are for the clean-up and containment of chemotherapy spills
FDA Devices Moderate May 15, 2019

ChemoPlus Chemo Spill Kit, Home Health Kit Product Code:DP5108K Product Usage: ChemoPlus chemotherapy spill kits are for the clean-up and containment of chemotherapy spills
FDA Devices Moderate May 15, 2019

ChemoPlus Protective Wrap-around Goggles Product Code:DP5030G Product Usage: ChemoPlus chemotherapy spill kits are for the clean-up and containment of chemotherapy spills
FDA Devices Moderate May 15, 2019

ChemoPlus Chemo Spill Kit Product Code:DP5016K Product Usage: ChemoPlus chemotherapy spill kits are for the clean-up and containment of chemotherapy spills
FDA Devices Moderate Mar 6, 2019

Curity All Purpose Sponges, Non-woven, 4 Ply, 4" x 4" (10.2 cm x 10.2 cm) Product Code: 8044 - Product Usage: Ideal for applying ointments, prepping, wiping needles, cleaning slides and more Rayon/polyester blend construction Highly absorbent.
FDA Devices Moderate Dec 26, 2018

Protexis Neoprene Surgical Glove, Size 8.5 This powder-free sterile light brown colored surgeons gloves are a disposable device made of synthetic rubber intended to be worn by operating room personnel to protect a surgical wound from contamination.
FDA Devices Moderate Dec 26, 2018

Protexis Neoprene Surgical Glove, Size 5.5 This powder-free sterile light brown colored surgeons gloves are a disposable device made of synthetic rubber intended to be worn by operating room personnel to protect a surgical wound from contamination.
FDA Devices Moderate Dec 26, 2018

Protexis Neoprene Surgical Glove, Size 9.0 This powder-free sterile light brown colored surgeons gloves are a disposable device made of synthetic rubber intended to be worn by operating room personnel to protect a surgical wound from contamination.
FDA Devices Moderate Dec 26, 2018

Protexis Neoprene Surgical Glove, Size 6.5 This powder-free Surgeon s glovessterile light brown colored surgeons gloves are a disposable device made of synthetic rubber intended to be worn by operating room personnel to protect a surgical wound from contamination.
FDA Devices Moderate Dec 26, 2018

Protexis Neoprene Surgical Glove, Size 7.5 This powder-free sterile light brown colored surgeons gloves are a disposable device made of synthetic rubber intended to be worn by operating room personnel to protect a surgical wound from contamination.
FDA Devices Moderate Dec 26, 2018

Protexis Neoprene Surgical Glove, Size 7.0 This powder-free sterile light brown colored surgeons gloves are a disposable device made of synthetic rubber intended to be worn by operating room personnel to protect a surgical wound from contamination.
FDA Devices Moderate Dec 26, 2018

Protexis Neoprene Surgical Glove, Size 6.0 This powder-free sterile light brown colored surgeons gloves are a disposable device made of synthetic rubber intended to be worn by operating room personnel to protect a surgical wound from contamination.
FDA Devices Moderate Dec 26, 2018

Protexis Neoprene Surgical Glove, Size 8.0 This powder-free sterile light brown colored surgeons gloves are a disposable device made of synthetic rubber intended to be worn by operating room personnel to protect a surgical wound from contamination.
FDA Devices Moderate Jul 25, 2018

Hydroline Trumpet Valve, Trumpet Valve, 5mm x 28cm Probe, Double Spike, Ref ASU1211, packaged 1/box, 12 boxes/case, single use, RX, Sterile. Manufactured For Cardinal Health, Waukegan, IL.
FDA Devices Moderate Jul 25, 2018

Hydroline Trumpet Valve with Pulse Wave Cassette, Trumpet Valve with Cassette, 5mm x 33cm Composite Probe, Double Spike, Ref ASC1201, packaged 1/box, 12 boxes/case, single use, RX, Sterile.
FDA Devices Moderate Jul 25, 2018

Hydroline Trumpet Valve, Trumpet Valve, 5mm x 33cm Probe, Single Spike, Ref ASU1200, packaged 1/box, 12 boxes/case, single use, RX, Sterile.
FDA Devices Moderate Jul 25, 2018

Hydroline Trumpet Valve with Pulse Wave Cassette, Trumpet Valve with Single Spike and no Probe, Ref ASC1220, packaged 1/box, 12 boxes/case, single use, RX, Sterile.
FDA Devices Moderate Jul 25, 2018

Hydroline Trumpet Valve with Pulse Wave Cassette, Trumpet Valve with Cassette, 5mm x 33cm Composite Probe, Single Spike, Ref ASC1200, packaged 1/box, 12 boxes/case, single use, RX, Sterile.
FDA Devices Moderate Jul 25, 2018

Hydroline Trumpet Valve, Trumpet Valve, 5mm x 28cm Probe, Single Spike, Ref ASU1210, packaged 1/box, 12 boxes/case, single use, RX, Sterile. .

Cardinal Health 200, LLC carries an outsized archive share

Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.

Similar medical devices volume

Nearest multi-notice firms that share this firm's dominant product category.

Smiths Medical Asd, Inc. 293 Cook Inc. 264 The Anspach Effort, Inc. 261 Smith & Nephew, Inc. 258

Frequently Asked Questions

How many federal recall notices name Cardinal Health 200, LLC? ▼
PlainRecalls indexes 285 distinct federal recall events naming Cardinal Health 200, LLC, 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 Cardinal Health 200, LLC sit among other recalling firms? ▼
Cardinal Health 200, LLC ranks #39 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 Cardinal Health 200, LLC's notices? ▼
FDA Devices accounts for 284 of this firm's 285 indexed notices across 2 issuing agencies.
What product category dominates Cardinal Health 200, LLC's filing book? ▼
Filings for Cardinal Health 200, LLC span 2 product categories, 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.
Cardinal Health 200, LLC: 285 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 Cardinal Health 200, LLC; individual notices remain authoritative on each linked recall page.

Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026