FDA Device Intelligence
Home › STRYKER SUSTAINABILITY SOLUTIONS, INC. › N/A

N/A

STRYKER SUSTAINABILITY SOLUTIONS, INC. · Model N/A · UDI-DI 00885825002145

NLH Prescription
1
510(k) clearances
449
Adverse events (1 deaths)
48
Recalls
11
Facilities

Description

Diagnostic EP Catheter D-Curve (Damato/BLU) ,5mm electrodes, 5mm spacing, 6F

Recalls

DateFirmReason
2026-05-15Medline Industries, LPExpansion of RES 98277. Specific lots of reprocessed catheters may contain small particles of residual material. If devices with residual particulates on patient-contacting surface
2026-04-10Stryker Sustainability SolutionsIncomplete seals on sterile product
2026-04-10Stryker Sustainability SolutionsIncomplete seals on sterile product
2026-04-10Stryker Sustainability SolutionsIncomplete seals on sterile product
2026-04-10Stryker Sustainability SolutionsIncomplete seals on sterile product
2026-04-10Stryker Sustainability SolutionsIncomplete seals on sterile product
2026-04-10Stryker Sustainability SolutionsIncomplete seals on sterile product
2026-04-10Stryker Sustainability SolutionsIncomplete seals on sterile product
2026-04-10Stryker Sustainability SolutionsIncomplete seals on sterile product
2026-04-10Stryker Sustainability SolutionsIncomplete seals on sterile product

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
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.