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Channel Drain

C. R. Bard, Inc. · Model V072227 · UDI-DI 00801741119132

GBX Prescription
10
510(k) clearances
5,886
Adverse events (26 deaths)
82
Recalls
239
Facilities

Description

Novaplus Channel Drain, 10Fr. Round Hubless Full Fluted Silicone with 3.2mm Trocar

Recalls

DateFirmReason
2026-03-05Cook IncorporatedProducts from the affected device lots were labeled with expiration dates that exceed the true shelf life.
2025-11-07Rocket Medical PlcIFU and device kit labeling contains misleading statements leading to improper securing of the device resulting in the potential to fall out during use.
2025-11-07Rocket Medical PlcIFU and device kit labeling contains misleading statements leading to improper securing of the device resulting in the potential to fall out during use.
2025-11-07Rocket Medical PlcIFU and device kit labeling contains misleading statements leading to improper securing of the device resulting in the potential to fall out during use.
2025-11-07Rocket Medical PlcIFU and device kit labeling contains misleading statements leading to improper securing of the device resulting in the potential to fall out during use.
2025-11-07Rocket Medical PlcIFU and device kit labeling contains misleading statements leading to improper securing of the device resulting in the potential to fall out during use.
2025-11-07Rocket Medical PlcIFU and device kit labeling contains misleading statements leading to improper securing of the device resulting in the potential to fall out during use.
2024-03-27Cardinal Health 200, LLCCardinal Health is issuing a lot number specific voluntary removal of Jackson-Pratt 3-Spring Reservoir kits due to specific products being shipped to users before undergoing steril
2024-03-27Cardinal Health 200, LLCCardinal Health is issuing a lot number specific voluntary removal of Jackson-Pratt 3-Spring Reservoir kits due to specific products being shipped to users before undergoing steril
2024-03-27Cardinal Health 200, LLCCardinal Health is issuing a lot number specific voluntary removal of Jackson-Pratt 3-Spring Reservoir kits due to specific products being shipped to users before undergoing steril

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.