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Fisherbrand

FISHER SCIENTIFIC COMPANY L.L.C. · Model 31323176 · UDI-DI 00613647000441

MMK
10
510(k) clearances
982
Adverse events (2 deaths)
3
Recalls
94
Facilities

Description

INPATIENT CL/TOP RD BASE 5QT

Recalls

DateFirmReason
2006-08-23Bemis Health Care,IncThe 5 Quart Wall Safes are shipped as two pieces (bottom & top) that customers are unable to assemble because of excess warp in the back wall of the container.
2006-04-03EM Innovations IncThe firm failed to include User Instructions with the Stic Kit Needle Containment Device, Model EMI 82691, which they shipped to distributor/customers.
2004-02-25Bemis Manufacturing Co.The closure flap of the recalled sharps containers have two tabs that fit into slots on the cover for final closure and locking but some of the covers have one of the tabs that wil

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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.