PlainRecalls

Cardinal Health

Compiled from official public sources by the editorial team.

75 recalls on record · Latest: Dec 14, 2022

Cardinal Health Recall Insight

Cardinal Health appears on 75 federal recall records indexed by PlainRecalls, out of 101,704 total recalls tracked across the FDA, CPSC, and NHTSA. That represents approximately 0.074% 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 Dec 14, 2022, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 25 entries, severity tagging shows 0 critical, 24 moderate, and 1 lower-severity recalls. Affected-unit counts are disclosed on 25 of 25 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 3 distinct product categories, with issuing agencies dominated by FDA Devices (23), FDA Drug (1), FDA Food (1). The date window on this page runs from Jan 30, 2013 to Feb 12, 2020.

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 Feb 12, 2020

AAMI 3 ROYALSILK SCRBNURGOWN BNS L, Gown. Item Code 90280NC

FDA Devices Moderate Feb 12, 2020

AAMI 3 FABRIC REINFORCEDGown 2XL NS, Item Code 9571NA

FDA Devices Moderate Feb 12, 2020

AAMI 3 NONREINF SURG GOWN 2XL XLONG, Item Code 9575EL

FDA Devices Moderate Feb 12, 2020

AAMI 3 NONREIN SURGGOWN BNS XL, Item Code 9545NC

FDA Devices Moderate Feb 12, 2020

AAMI 3 FABRIC REINF SURG GOWN 2XL, Item Code 9571

FDA Devices Moderate Feb 12, 2020

AAMI 3 NON-RNF SURG GOWN 3XL LONG, Item Code 95995N

FDA Devices Moderate Feb 12, 2020

AAMI 3 ROYALSILK SURGGOWN BNS 2XL, Item Code 9578NB

FDA Devices Moderate Feb 12, 2020

AAMI 3 FABRNF SCRUB SURG GWN XL NS, Gown. Item Code 91070NB

FDA Devices Moderate Feb 12, 2020

AAMI 3 FABREINF SURG GOWN LARGE, Item Code 9511

FDA Devices Moderate Oct 12, 2016

BLUE IMPERVIOUS GOWN WITH THUMBHOOKS, X-LARGE. Non-Sterile, Single Use Only, Plastic Non-Surgical Isolation Gown Non-Sterile, Single Use Only, Plasti…

FDA Devices Moderate Sep 7, 2016

The 9025TRU Arterial Blood Gas (ABG) Kit is used to obtain arterial blood sampling for pH, Blood Gas, Electrolyte and Metabolite Analysis.

FDA Devices Moderate Apr 13, 2016

Gomco Style Circumcision Clamp Trays is an instrument used to compress the foreskin of the penis during circumcision of a male infant.

FDA Devices Moderate Oct 28, 2015

Ambitex NMD400 Nitrile Exam Gloves size medium. General Hospital and Personal use. Intended to be worn on the hand for medical purposes to provide…

FDA Drug Low Apr 22, 2015

Potassium Chloride, microencapsulated extended-release tablets, 20 mEq, blister card of 30/10 cards in a corrugated shipper, Rx only, Manufactured by…

FDA Devices Moderate Feb 11, 2015

Lubricated Intubating Stylet 6FR that is inserted into an endotracheal tube to facilitate intubation. This product is used in surgical or medical eme…

FDA Devices Moderate Apr 3, 2013

Needle Counters with Blade Disarmer; 12.2 x 10.5 x 1.7 cm; 30 Count/60 Capacity; Sterile; Foam Strip; Magnetic Area (Cat. No. 4FS60SSA) Needle Cou…

FDA Devices Moderate Apr 3, 2013

Needle Counters with Blade Disarmer; 11.5 x 6.5 x 3.3 cm; 15 Count/30 Capacity; Sterile; Removable Numbered Foam Block; Magnetic Area (Cat. No. 4FS30…

FDA Devices Moderate Apr 3, 2013

Needle Counters; 11.5 x 6.5 x 3.3 cm; 20 Count/40 Capacity; Sterile; Removable Numbered Foam Block; Adhesive Area (Cat. No. 3FA40SSA) Needle Count…

FDA Devices Moderate Apr 3, 2013

Needle Counters; 12.2 x 10.5 x 3.5 cm; 40 Count/80 Capacity; Sterile; Double Removable Numbered Foam Blocks (Cat. No. 3FF80SSA) Product Usage: Di…

FDA Devices Moderate Apr 3, 2013

Needle Counters; Sterile; Foam Strip; 12.2 x 10.5 x 1.7 cm; 30 Count/60 Capacity; Sterile; Foam Strip; Magnetic Area (Cat. No. 3FS60SSA) Needle Co…

FDA Devices Moderate Apr 3, 2013

Needle Counters with Blade Disarmer; 12.2 x 10.5 x 3.5 cm; 40 Count/70 Capacity; Sterile; Removable Numbered Foam Block; Adhesive Area (Cat. No. 4FA7…

FDA Devices Moderate Apr 3, 2013

Needle Counters; 12.2 x 10.5 x 3.5 cm; 40 Count/70 Capacity; Sterile; Removable Numbered Foam Block; Adhesive Area (Cat. No. 3FA70SSA) Needle Coun…

FDA Devices Moderate Apr 3, 2013

Needle Counters with Blade Disarmer; 12.2 x 10.5 x 3.5 cm; 60 Count/100 Capacity; Sterile; Removable Numbered Foam Block; Double Numbered Magnets (Ca…

FDA Devices Moderate Apr 3, 2013

Needle Counters with Blade Disarmer; 11.5 x 6.5 x 3.3 cm; 20 Count/40 Capacity; Sterile; Removable Numbered Foam Block; Adhesive Area (Cat. No. 4FA40…

FDA Food Moderate Jan 30, 2013

Dairy Aid Lactase Enzyme Supplement, Caplet, 3,000 FCC Units, 60 caplets, OTC, Repackaged by: Cardinal Health, Zanesville, OH 43701, NDC 55154-1335-4

Nearby Manufacturers

Other firms with recall activity tracked in the PlainRecalls index.

Compare Cardinal Health with Zimmer Biomet, Inc. →

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.