Cardinal Health Inc. recalls
Every recall we track for Cardinal Health Inc. — 240 in all, from 2018–2025 — plus the complaints and injury reports the public filed about them. 2 are rated “stop using now”.
Recalls per year, by danger level
Recalls from Cardinal Health Inc. peaked in 2021 (213); 240 since 2017. 1% rated “stop using now”.
All FDA recall records for Cardinal Health Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 1 | 1 |
| 2019 | 1 | 0 | 8 | 0 | 9 |
| 2020 | 0 | 0 | 3 | 0 | 3 |
| 2021 | 0 | 0 | 205 | 8 | 213 |
| 2022 | 0 | 0 | 3 | 0 | 3 |
| 2023 | 1 | 1 | 4 | 0 | 6 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 5 | 0 | 5 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
Most common reasons for Cardinal Health Inc. recalls
What to do if you have a recalled Cardinal Health Inc. product
- Match the NDC and lot number on your bottle or box to the recall.
- Don’t stop a prescription on your own — ask your pharmacist or doctor for a replacement first.
- Report side effects to FDA MedWatch.
All Cardinal Health Inc. recalls
12 shown- Lower riskDrug
Cardinal Health Inc. recalls Enoxaparin Sodium Injection, USP, 30 mg/0.3 mL, packaged in 0.3 mL prefilled syringes further packaged in bags of 5
Cardinal Health recalls Enoxaparin Sodium Injection 30mg/0.3mL prefilled syringes packaged in bags of 5 due to mislabeled product. The bags intended for 80mg/0.8mL contain 30mg/0.3mL instead.
Cardinal HealthAug 5, 2025 - Lower riskDrug
Cardinal Health Inc. recalls RECOMBINATE, [Antihemophilic Factor (Recombinant)], 5 mL vials, Rx Only, Takeda Pharmaceuticals USA, Cambridge, MA
Cardinal Health recalls RECOMBINATE antihemophilic factor vials due to temperature exposure during storage. Affected lots expire 03/18/2026 and 10/18/2025. Contact Takeda for details.
Takeda Pharmaceuticals USAJul 30, 2025 - Lower riskDrug
Cardinal Health Inc. recalls Wegovy (semaglutide) injection, 2.4 mg/0.75 mL, 4 Single-Dose Prefilled Pens per Carton, For Subcutaneous Use Only, Rx
Cardinal Health recalls Wegovy (semaglutide) injections due to potential temperature exposure during shipping. This may cause product instability. Check your lot number and contact Novo Nordisk for details.
Cardinal HealthApr 9, 2025 - Lower riskDrug
Cardinal Health Inc. recalls LEADER brand Dry Eye Relief (Polyethylene Glycol 400, 0.4% Propylene Glycol, 0.3%); 0.33 FL OZ (10 mL) dropper bottle,
Cardinal Health recalls LEADER Dry Eye Relief (0.33 fl oz) due to non-sterility found at manufacturing facility. FDA detected bacterial contamination in environmental samples.
LEADEROct 31, 2023 - Lower riskDrug
Cardinal Health Inc. recalls Trulicity (dulaglutide) injection, 0.75 mg/0.5mL once weekly, 4 Single-Dose Pens, Rx only, Eli Lilly and Company,
Eli Lilly recalls Trulicity injections that may have been exposed to improper temperatures. This could affect product stability and safety. Check your product details to see if you are affected.
Eli LillyApr 5, 2022 - Lower riskMedical device
Cardinal Health Inc. recalls OPTICHAMBER DIAMOND SPACER WITH LARGE MASK Item Number: 4742326
Cardinal Health recalls Diamond Spacer with Large Mask (Item 4742326) due to temperature exposure during shipping, which may cause inaccurate results. Affected units shipped between Feb 23, 2021 and March 10, 2021.
Cardinal HealthMar 16, 2021 - Lower riskDrug
Cardinal Health Inc. recalls Edarbi (azilsartan medoxomil) tablets 80 mg 30 Tablets Rx Only NDC 60631-080-30 Manufactured for: arbor Pharmaceuticals
Cardinal Health recalls Edar: 80mg tablets due to potential temperature exposure during storage. This may affect drug stability. Check NDC 60631-080-30 for affected units.
Cardinal HealthMar 15, 2021 - Lower riskDrug
Cardinal Health Inc. recalls Tremfya (guselkumab) Injection, 100 mg/mL, one single-dose prefilled syringe per carton, Rx only, Manufactured by:
Cardinal Health recalls Tremfya (guselkumab) injections due to temperature abuse risks. This product may be unsafe if exposed to high temperatures.
Cardinal HealthMar 9, 2021 - Lower riskMedical device
Cardinal Health Inc. recalls Professional Urine Drug Control, Item code 88010 - Product Usage: The Alere Professional Cup Urine Drug Controls are
Cardinal Health recalls Alere Professional Urine Drug Controls with improper refrigeration causing misdiagnosis. Affected units may lead to incorrect test results if stored outside approved temperatures.
AlereApr 20, 2020 - Lower riskMedical device
Cardinal Health Inc. recalls Kangaroo Connect ENPlus Spike Set Anti-free Flow, Product Code 77000FD
Cardinal Health recalls Kangaroo Connect ENPlus Spike Set Anti-free Flow (Product Code 77000FD) due to potential leaks at the tube and spike connector interface. All units are affected.
Cardinal HealthDec 26, 2019 - Lower riskMedical device
Cardinal Health Inc. recalls Cordis Precise Nitinol Stent System. The Cordis PRECISE Nitinol Stent System devices are designed to deliver a
Cardinal Health recalls PRECISE Nitinol Stent Systems with incorrect MRI labeling. The devices are labeled "MRI Safe" instead of "MRI Conditional". This could cause issues with MRI scans. Consumers should check their product codes.
Cardinal HealthNov 14, 2019 - UnratedMedical device
Cardinal Health Inc. recalls Presource Kit Total Joint Pack containing a double-wrapped basin component. Product Usage: This kit is used on patients
Cardinal Health recalls Presource Kit Total Joint Pack with double-wrapped basin component due to sterility assurance validation issues. Affected units sold with specific lot numbers.
Cardinal HealthNov 16, 2018
Cardinal Health Inc. recall questions
How many recalls has Cardinal Health Inc. had?
240 recalls from Cardinal Health Inc. are on record with U.S. safety agencies, from 2018–2025 (213 drug, 27 medical device).
What is the most recent Cardinal Health Inc. recall?
Cardinal Health Inc. recalls Enoxaparin Sodium Injection, USP, 30 mg/0.3 mL, packaged in 0.3 mL prefilled syringes further packaged in bags of 5, dated Aug 5, 2025. Every Cardinal Health Inc. recall is listed on this page, newest first.
Why are Cardinal Health Inc. products recalled?
The most common reasons on record: CGMP Deviations: Intermittent exposure to temperature excursion during storage. (198).
What should I do if I have a recalled Cardinal Health Inc. product?
Match the NDC and lot number on your bottle or box to the recall. Don’t stop a prescription on your own — ask your pharmacist or doctor for a replacement first. Report side effects to FDA MedWatch.
How do I get alerts for new Cardinal Health Inc. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.