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CONMED

Conmed Corporation · Model HPP-B · UDI-DI 20653405023699

LRO Prescription
10
510(k) clearances
21,411
Adverse events (2 deaths)
1,059
Recalls
158
Facilities

Description

ECG LEADWIRES, TAB, .125" (3.2 MM) PIN, BIDIRECTIONAL CLIP 6" (15.2 CM) LONG

Recalls

DateFirmReason
2026-07-29Cardinal Health 200, LLCThe Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is
2026-07-20Medline Industries, LPDownstream recall - manufacturer recalled specific lots of BD ChloraPrep Clear - 1mL Applicators. Affected product may exhibit an open or incomplete seal on the packaging of the ap
2026-07-14Cardinal Health 200, LLCCardinal Health was recently informed of a medical device recall from MEDICOM concerning the Ritmed Neurological Sponges. The recall is being issued due to unexpected variability o
2026-07-14AVID Medical, Inc.Convenience kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which lacks sterility assurance due to to wrinkles in the paper lidding which may breach th
2026-07-10Medline Industries, LPKits contain a potentially contaminated component which were recalled by the manufacturer
2026-07-09AVID Medical, Inc.Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.
2026-07-09AVID Medical, Inc.Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.
2026-07-09AVID Medical, Inc.Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.
2026-07-09AVID Medical, Inc.Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.
2026-07-09AVID Medical, Inc.Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.

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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.