Teleflex Medical Europe Ltd
6 FDA 510(k) clearances · Recalling firm
◉ Watch Teleflex Medical Europe Ltd
| Record | Firm | Date |
|---|---|---|
| Teleflex MEDICAL Pilling(R) UNIVERSAL SHEARS 7 1/2", REF 142542 Product Usage: general sur recall (Z-2287-2018) | Teleflex Medical Europe Ltd | 2018-06-14 |
| Teleflex MEDICAL HUDSON RCI One Way Valve w. Capped Monitoring Port, REF 1644, QTY 50 Prod recall (Z-1403-2018) | Teleflex Medical Europe Ltd | 2018-04-17 |
| Latex Rebreathing Bags: Product Code Equivalent Code (a) 151174050 151174 (b) 153000005 15 recall (Z-1367-2018) | Teleflex Medical Europe Ltd | 2018-04-12 |
| Rectal Catheters; Product Code Equivalent Code 580114 580114 Product Usage: Rectal Balloon recall (Z-1368-2018) | Teleflex Medical Europe Ltd | 2018-04-12 |
| Simplastic Suprapubic Puncture Instruments: Product Code Equivalent Code (a) 650704100 551 recall (Z-1369-2018) | Teleflex Medical Europe Ltd | 2018-04-12 |
| Baker Jejunostomy Tubes: Product Code Equivalent Code (a) 655300160 655316 (b) 655500200 6 recall (Z-1370-2018) | Teleflex Medical Europe Ltd | 2018-04-12 |
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Every clearance here is in the API, with alerts when new ones post.