Tyco Healthcare/Kendall
Country not established
- Devices
- 4
- FDA recalls
- 6
At a glance
Market reach
- United States
- FDA recalls
What Tyco Healthcare/Kendall makes
The company manufactures sterile pre-filled sodium chloride flush syringes for intravenous use, portable venous thromboembolism prevention compression systems, enteral feeding pumps and associated feeding sets, and compression sleeves for deep vein thrombosis prophylaxis.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Kendall Monoject Pre-Fill Advanced 0.9%SODIUM Chloride Flush Syringes For Sterile Delivery Ref K060339
Regimes: 510(k) Registry: 510(k)Scd Express Portable Compression System Ref K040511
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
FDA recalls
FDA recall records list 6 recalls initiated by Tyco Healthcare/Kendall, initiated on 2003-03-20. By recorded status: 6 terminated. The reasons filed fall into these groups: other reasons as filed. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.
2003
- 20 Mar 2003 Z-0742-03 Unclassified (pre-2012) Terminated Tandem Hemodialysis Catheter may have splits in the catheter shaft below the extension adapter
- 20 Mar 2003 Z-0743-03 Unclassified (pre-2012) Terminated Tandem Hemodialysis Catheter may have splits in the catheter shaft below the extension adapter
- 20 Mar 2003 Z-0744-03 Unclassified (pre-2012) Terminated Tandem Hemodialysis Catheter may have splits in the catheter shaft below the extension adapter
- 20 Mar 2003 Z-0745-03 Unclassified (pre-2012) Terminated Tandem Hemodialysis Catheter may have splits in the catheter shaft below the extension adapter
- 20 Mar 2003 Z-0746-03 Unclassified (pre-2012) Terminated Tandem Hemodialysis Catheter may have splits in the catheter shaft below the extension adapter
- 20 Mar 2003 Z-0747-03 Unclassified (pre-2012) Terminated Tandem Hemodialysis Catheter may have splits in the catheter shaft below the extension adapter
Frequently asked questions
How many devices does Tyco Healthcare/Kendall have in the registry?
The registry currently lists 4 devices for Tyco Healthcare/Kendall. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tyco Healthcare/Kendall's devices?
Among its 4 most recently registered devices, Tyco Healthcare/Kendall has devices listed in FDA 510(k) (4 devices).
What risk classes do Tyco Healthcare/Kendall's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Tyco Healthcare/Kendall's devices are Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for Tyco Healthcare/Kendall?
FDA recall records list 6 recalls initiated by Tyco Healthcare/Kendall, the most recent initiated on 20 Mar 2003. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.
What are the newest devices from Tyco Healthcare/Kendall in the registry?
The most recently registered devices listed for Tyco Healthcare/Kendall include KENDALL MONOJECT PRE-FILL ADVANCED 0.9%SODIUM CHLORIDE FLUSH SYRINGES FOR STERILE DELIVERY, SCD EXPRESS PORTABLE COMPRESSION SYSTEM, KENDALL EPUMP ENTERAL FEEDING PUMP AND ENTERAL FEEDING SETS and KENDALL SCD SLEEVES (EXTRA LARGE KNEE, EXTRA LARGE THIGH), KENDALL SCD LEXPRES SLEEVES (EXTRA LARGE KNEE, EXTRA LARGE.