Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company recalls
Every recall we track for Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company — 18 in all, all from 2017 — plus the complaints and injury reports the public filed about them. 5 are rated “stop using now”.
Recalls per year, by danger level
Recalls from Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company peaked in 2017 (18); 18 since 2017. 28% rated “stop using now”.
All FDA recall records for Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company 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 | 5 | 4 | 6 | 3 | 18 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 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 Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company 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 Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company recalls
3 shown- Stop using nowMedical device
Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company recalls Irrisept OR, Finished Bottle Assembly 450 ml STEP 1
Smiths Medical recalls Irrisept OR 450ml bottles due to leaking containers that could expose users to infectious agents. Affected units include specific model and lot numbers.
Smiths MedicalSep 5, 2017 - Lower riskMedical device
Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company recalls Portex 5ml Normal Saline (0.9%) Unit Dose¿¿¿¿ ¿
Smiths Medical recalls Portex 5ml Normal Saline (0.9%) Unit Dose containers due to leaking containers that could expose users to infectious agents. Affected units have model # UD9005 and lot number B515.
Smiths MedicalSep 5, 2017 - Stop using nowDrug
Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company recalls Sterile Eyewash (sterile isotonic phosphate buffered saline solution), 4 oz. 24 units per box. Manufactured by Medex
Smiths Medical recalls 4 oz sterile eyewash bottles due to leaking containers that lack sterility assurance, posing an infection risk.
Smiths MedicalSep 5, 2017
Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company recall questions
How many recalls has Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company had?
18 recalls from Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company are on record with U.S. safety agencies, from 2017 (14 medical device, 4 drug).
What is the most recent Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company recall?
Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company recalls Irrisept OR, Finished Bottle Assembly 450 ml STEP 1, dated Sep 5, 2017. Every Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company recall is listed on this page, newest first.
What should I do if I have a recalled Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company 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 Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company 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.