The Recall Desk
HighFDA (Devices)·Z-1319-2026·Announced 2026-02-18

[pending] Medline ReNewal Reprocessed Webster CS Catheters: Webster CS Catheter 10 Electrodes 2-8-2mm Spaci

Pending LLM rewrite. Source: FDA_DEVICE Z-1319-2026.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: Pending LLM scoring against the rubric.

Plain-English summary

These lots of reprocessed catheters may contain small particles of residual material. If affected devices are used, there is a risk of inflammatory response, systemic infection, or granulomatous reaction or thrombus reaction which may lead to cerebral or pulmonary embolism, or deep vein thrombosis. Expansion of recall Z-2610/2614-2025

The recalled product

Product
Medline ReNewal Reprocessed Webster CS Catheters: Webster CS Catheter 10 Electrodes 2-8-2mm Spacing w/AutoID w/ EZ Steer BD710DF282CRH; Webster CS Catheter 10 Electrodes, 2-8-2mm Spacing w/ EZ Steer BD710DF282RRH BD710FJ282RRH; Webster CS Catheter 10 Electrodes, 2-8-2mm S
Manufacturer
Medline Industries, LP

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (3)

  • BD710DF282CRH UDI-DI 10197344044023 Lots EP250429 EP250808
  • BD710DF282RRH UDI-DI 10197344044030 Lots EP250429 EP250808
  • BD710FJ282RRH UDI-DI 10197344044054 Lots EP250429 EP250808

Distribution

Distributed nationwide across the United States.