CAREFUSION recalls
Every recall we track for CAREFUSION — 25 in all, from 2021–2022 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from CAREFUSION peaked in 2021 (16); 25 since 2017.
All FDA recall records for CAREFUSION 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 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 1 | 15 | 0 | 16 |
| 2022 | 0 | 0 | 9 | 0 | 9 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled CAREFUSION product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All CAREFUSION recalls
3 shown- Lower riskMedical device
CAREFUSION recalls BD MaxGuard Drop Administration set with 3 Needleless Y-Sites Removable 3-port Manifold and removable 4-way stopcock,
CAREFUSION recalls BD MaxGuard Drop Administration sets with incorrect 2027 expiration labels (should be 2025). Using expired sets may cause leaks and infection risks. Affected units have specific lot numbers.
CAREFUSIONAug 1, 2022 - Lower riskMedical device
CAREFUSION recalls BD Gravity Burette Set 60 DROP 1.2 MF 2 SmartSite VALVES BALL VALVE DRIP CHAMBER V/NV, REF: 10037031; BD Gravity
CAREFUSION recalls Gravity Burette Sets with potential flow problems that could delay medical therapy. Affected models include 60-drop sets with specific serial numbers. Contact CAREFUSION for details.
CAREFUSIONAug 2, 2021 - Lower riskMedical device
CAREFUSION recalls MaxPlusTM bi fuse extension set with 2 clear needleless connectors - Product Usage: The needleless connector can be
CAREFUSION recalls MaxPlus bi fuse extension sets with 2 clear needleless connectors due to leakage issues in validation testing. Affected units may not meet safety standards for medical use.
CAREFUSIONJun 9, 2021
CAREFUSION recall questions
How many recalls has CAREFUSION had?
25 recalls from CAREFUSION are on record with U.S. safety agencies, from 2021–2022.
What is the most recent CAREFUSION recall?
CAREFUSION recalls BD MaxGuard Drop Administration set with 3 Needleless Y-Sites Removable 3-port Manifold and removable 4-way stopcock,, dated Aug 1, 2022. Every CAREFUSION recall is listed on this page, newest first.
What should I do if I have a recalled CAREFUSION product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new CAREFUSION 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.