Data Foundry

Medical device recalls 2026

Medline ReNewal Reprocessed Webster CS Catheters: Webster CS Catheter… — Class I medical device recall Z-1319-2026

Ongoing recall by Medline Industries, LP, reported 2026-02-18, distributed nationwide. These lots of reprocessed catheters may contain small particles of residual material. If affected devices are

Recall numberZ-1319-2026
Product typeMedical device
ClassificationClass I
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmMedline Industries, LP, Northfield, IL, United States
Recall initiated2025-12-22
Classified2026-02-06
Reported by FDA2026-02-18
DistributedNationwide (US)
Quantity228
UPC / GTIN / UDI-DI10197344044023, 10197344044030, 10197344044047, 10197344044054, 40197344044048
Lot numbersBD710DF282RRH, BD710FJ282CRH, BD710FJ282RRH, EP250429, EP250808

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 Spacing w/AutoID w/ EZ Steer BD710FJ282CRH;

Reason for recall

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

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1319-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.