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MEDLINE INDUSTRIES, INC. · Model 401780RH · UDI-DI 10197344020973
NLH
Prescription
1
510(k) clearances
451
Adverse events (1 deaths)
48
Recalls
11
Facilities
Description
DIAG EP CATH QUAD MED SWEEP 5-5-5 5FR
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-05-15 | Medline Industries, LP | Expansion of RES 98277. Specific lots of reprocessed catheters may contain small particles of residual material. If devices with residual particulates on patient-contacting surface |
| 2026-04-10 | Stryker Sustainability Solutions | Incomplete seals on sterile product |
| 2026-04-10 | Stryker Sustainability Solutions | Incomplete seals on sterile product |
| 2026-04-10 | Stryker Sustainability Solutions | Incomplete seals on sterile product |
| 2026-04-10 | Stryker Sustainability Solutions | Incomplete seals on sterile product |
| 2026-04-10 | Stryker Sustainability Solutions | Incomplete seals on sterile product |
| 2026-04-10 | Stryker Sustainability Solutions | Incomplete seals on sterile product |
| 2026-04-10 | Stryker Sustainability Solutions | Incomplete seals on sterile product |
| 2026-04-10 | Stryker Sustainability Solutions | Incomplete seals on sterile product |
| 2026-04-10 | Stryker Sustainability Solutions | Incomplete seals on sterile product |
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Get your free API keyRead the docsData 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.