Carefusion 2200 Inc recalls
Every recall we track for Carefusion 2200 Inc — 97 in all, from 2013–2023 — plus the complaints and injury reports the public filed about them. 3 are rated “stop using now”.
Recalls per year, by danger level
Recalls from Carefusion 2200 Inc peaked in 2022 (63); 95 since 2017. 3% rated “stop using now”.
All FDA recall records for Carefusion 2200 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 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 2 | 5 | 8 | 0 | 15 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 1 | 0 | 57 | 5 | 63 |
| 2023 | 0 | 7 | 10 | 0 | 17 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
Carefusion 2200 Inc recalls before 2017
Recalls on record by year.
What to do if you have a recalled Carefusion 2200 Inc 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 2200 Inc recalls
9 shown- Use cautionMedical device
Carefusion 2200 Inc recalls Snowden-Pencer MIS DIAMOND-TOUCH CLAMP BOWEL 50 MM JAW 5MM, 32CM, RATCHETED, REF SP90-7045; endoscopic surgical device
Carefusion 2200 recalls specific lots of their Diamond-Touch Bowel Clamp for potential rotation knob cracking from manufacturing adhesive issues. Affected units have UDI/DI 10885403160561 and Lot B23. Contact for remedy.
Carefusion 2200Jul 13, 2023 - Lower riskMedical device
Carefusion 2200 Inc recalls (1) Carefusion V. Mueller Graves Vaginal Speculum, Catalog #GL11, Medium Blade, 4 x 1 3/8" (10.2 X 3.5cm); and (2)
Carefusion recalls two vaginal specula models (GL11 and GL31) with incorrect labeling causing product mix-ups. Affected units have specific lot numbers and sizes. Consumers should check their specula for label errors.
CarefusionMar 16, 2023 - Lower riskMedical device
Carefusion 2200 Inc recalls CD5 Series of Genesis Reusable Rigid Sterilization Container Systems catalog number and product name: 1. CD5-3B,
Carefusion recalls CD5 Series Genesis Reusable Rigid Sterilization Containers due to potential sterility breaches. These containers may hold surgical equipment that becomes contaminated after expiration.
CarefusionJan 30, 2023 - Lower riskMedical device
Carefusion 2200 Inc recalls Carefusion V. Mueller" CUSHING BAYONET BIPOLAR FORCEPS, 2.0MM TIP, INSULATED OVERALL LENGTH 7-1/2" (190MM), REF F-2004
Carefusion recalls specific bipolar forceps due to missing instructions for power supply and cleaning. Owners should check model numbers and contact Carefusion for details.
CarefusionNov 2, 2022 - UnratedMedical device
Carefusion 2200 Inc recalls CareFusion V.Mueller GENESIS FULL-LENGTH CONTAINER 23 X12" (58.4 X 30.5CM) 6" (15.2CM) DEEP STERRAD COMPATIBLE, REF
Carefusion recalls Genesis STERRAD reusable sterilization containers that failed aerosol challenge testing. These containers may not meet safety standards for sterilization processes.
CarefusionSep 26, 2022 - Lower riskMedical device
Carefusion 2200 Inc recalls (a) CareFusion Snowden-Pencer Plastics, Endoplastic Endoscope 10 mm, 30 degrees 7", 17.5 cm, Catalog #88-5910; (b)
Carefusion recalls four endoscope models due to missing instruction manual in packaging. This could lead to improper use if the user doesn't know how to operate the device correctly.
CarefusionFeb 23, 2022 - Lower riskMedical device
Carefusion 2200 Inc recalls Safe-T PLUS Thora-Para 5 Fr Catheter Drainage Tray
Carefusion recalls Safe-T PLUS Thora-Para 5 Fr Catheter Drainage Tray due to potential air leaks from valves, which could introduce up to 30cc of air into patients. Affected units have specific catalog and batch numbers.
CarefusionMay 28, 2020 - Use cautionMedical device
Carefusion 2200 Inc recalls Mueller Knife Handle, Hexagonal - Product Usage: Intended to hold surgical blades.
Carefusion recalls Mueller Knife Handles (OP0702/OP0703) due to potential loose blades causing injury during surgery. Affected units sold with specific model and lot numbers.
CarefusionMay 18, 2020 - Use cautionDrug
Carefusion 2200 Inc recalls CareFusion Scrub Care Surgical Scrub Brush-Sponge/Nail Cleaner With 15% Povidone-iodine (USP) Surgical Hand Scrub;
CareFusion recalls 1.66M surgical scrub brushes because available iodine is less than labeled. Check your NDC and lot number for details.
CareFusionDec 20, 2013
Carefusion 2200 Inc recall questions
How many recalls has Carefusion 2200 Inc had?
97 recalls from Carefusion 2200 Inc are on record with U.S. safety agencies, from 2013–2023 (95 medical device, 2 drug).
What is the most recent Carefusion 2200 Inc recall?
Carefusion 2200 Inc recalls Snowden-Pencer MIS DIAMOND-TOUCH CLAMP BOWEL 50 MM JAW 5MM, 32CM, RATCHETED, REF SP90-7045; endoscopic surgical device, dated Jul 13, 2023. Every Carefusion 2200 Inc recall is listed on this page, newest first.
What should I do if I have a recalled Carefusion 2200 Inc 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 2200 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.