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Medicon

Medicon eG. Chirurgiemechaniker-Genossenschaft · Model 224.11.61 · UDI-DI 04046826174699

LRW Prescription
10
510(k) clearances
795
Adverse events (1 deaths)
20
Recalls
514
Facilities

Description

MC Siegert scrs cvd 11.5cm

Recalls

DateFirmReason
2025-11-13Medline Industries, LPThe items may have weak packaging seals that may result in a breach of sterility if the seal fails and may lead to an increased risk of infection if product is utilized.
2025-11-13Medline Industries, LPThe items may have weak packaging seals that may result in a breach of sterility if the seal fails and may lead to an increased risk of infection if product is utilized.
2024-12-03Sklar InstrumentsReports of various packaging issues that may result in a breach of the sterile barrier.
2024-11-12MEDLINE INDUSTRIES, LP - NorthfieldWeak seals may result in a breach of sterility, which may not be detectable to the user. This can lead to increased risk of contamination and infection.
2024-10-21MEDLINE INDUSTRIES, LP - NorthfieldTip protector may fall off within the packaging, resulting in compromised sterile barrier system and loss of sterility.
2024-04-08MEDLINE INDUSTRIES, LP - NorthfieldMedical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that ma
2024-02-23MEDLINE INDUSTRIES, LP - NorthfieldProduct may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
2023-11-16Steris CorporationBandage Scissors handle cover component contains an incorrect color masterbatch resin carrier. This may allow a pink dye/residue to appear on the Bandage Scissors and/or sterilizat
2022-07-25Stradis Medical, LLC dba Stradis HealthcareThe sterile barrier may be compromised.
2018-06-12Teleflex Medical Europe LtdThe incorrect plastic was used to manufacture the handles of these shears, which causes the handles to melt if sterilized.

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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.