Teleflex Medical Europe Ltd recalls
Every recall we track for Teleflex Medical Europe Ltd — 11 in all, from 2018–2021 — plus the complaints and injury reports the public filed about them. 1 is rated “stop using now”.
Recalls per year, by danger level
Recalls from Teleflex Medical Europe Ltd peaked in 2018 (7); 11 since 2017. 9% rated “stop using now”.
All FDA recall records for Teleflex Medical Europe Ltd 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 | 1 | 3 | 3 | 0 | 7 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 4 | 0 | 0 | 4 |
| 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 Teleflex Medical Europe Ltd 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 Teleflex Medical Europe Ltd recalls
5 shown- Use cautionMedical device
Teleflex Medical Europe Ltd recalls RUSCH Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF numbers: a) 170050 b) 170055 c) 170060 d)
RUSCH Slick Set Cuffed Endotracheal Tubes with specific REF and lot numbers recalled due to potential cuff inflation while pilot balloon remains flat.
RUSCHJul 16, 2021 - Stop using nowMedical device
Teleflex Medical Europe Ltd recalls Teleflex MEDICAL Pilling(R) UNIVERSAL SHEARS 7 1/2", REF 142542 Product Usage: general surgical scissors
Teleflex Medical Europe recalls universal surgical shears with handles that melt during sterilization. Affected lot numbers F7 and G7. Stop using immediately to prevent injury.
Teleflex MedicalJun 12, 2018 - Use cautionMedical device
Teleflex Medical Europe Ltd recalls Teleflex MEDICAL HUDSON RCI One Way Valve w. Capped Monitoring Port, REF 1644, QTY 50 Product Usage: for use in
Teleflex Medical recalls Hudson RCI One Way Valve (REF 1644) due to potential disconnection causing ventilation interruption. Affected units sold in respiratory/anesthesia circuits.
Teleflex MedicalMar 27, 2018 - Lower riskMedical device
Teleflex Medical Europe Ltd recalls Teleflex MEDICAL LMA(TM) MADgic(TM) LARYNGO-TRACHEAL MUCOSAL ATOMIZATION DEVICE, MAD700, QTY: 1 Intended for the
Teleflex Medical recalls MAD700 laryngotracheal mucosal atomization device due to potential missing or incomplete package label information. Affected units may not have proper labeling for topical anesthetic use.
Teleflex MedicalMar 19, 2018 - Use cautionMedical device
Teleflex Medical Europe Ltd recalls Simplastic Suprapubic Puncture Instruments: Product Code Equivalent Code (a) 650704100 551310 (b) 650704120 551312 (c)
Teleflex Medical recalls Simplastic suprapubic puncture instruments with latex that may cause allergic reactions. Affected products include specific model codes and batch numbers. Consumers should check packaging for the allergy warning.
Teleflex MedicalMar 15, 2018
Teleflex Medical Europe Ltd recall questions
How many recalls has Teleflex Medical Europe Ltd had?
11 recalls from Teleflex Medical Europe Ltd are on record with U.S. safety agencies, from 2018–2021.
What is the most recent Teleflex Medical Europe Ltd recall?
Teleflex Medical Europe Ltd recalls RUSCH Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF numbers: a) 170050 b) 170055 c) 170060 d), dated Jul 16, 2021. Every Teleflex Medical Europe Ltd recall is listed on this page, newest first.
What should I do if I have a recalled Teleflex Medical Europe Ltd 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 Teleflex Medical Europe Ltd 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.