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SUSI

Aesculap AG · Model BC606SU · UDI-DI 04046963892739

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

Description

METZENBAUM SUSI Dissecting Scissors, curved, 7", (180 mm), sterile, disposable, pack of 20 pcs, single packed

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.