FDA Device Intelligence
Home › FISHER SCIENTIFIC COMPANY L.L.C. › Sure-Vue

Sure-Vue

FISHER SCIENTIFIC COMPANY L.L.C. · Model 23-200-277 · UDI-DI 00613647000304

MHI Prescription
10
510(k) clearances
2
Adverse events
6
Recalls
17
Facilities

Description

Sure-Vue Signature Cryptosporidium and Giardia Test Kit

Recalls

DateFirmReason
2025-11-03GET TESTED INTERNATIONAL ABDistribution without premarket approval/clearance.
2025-03-24MEDLINE INDUSTRIES, LP - NorthfieldA single lot of the ImmunoCard STAT! Crypto/Giardia Test Kit was inadvertently stored in Medline warehouses at temperatures outside of the labeled storage requirements.
2008-08-11Remel, IncFaint grey test lines for Cryptosporidium may be visible which may be interpreted as false positive
2004-02-23Genzyme DiagnosticsFalse Positive results.
2003-12-09Remel, Inc.The conjugate may cause the negative control to produce high OD readings, therefore invalidating the run.
2002-11-21Remel, Inc.The conjugate of the ProSpecT Giardia/Cryptosporidium Microplate Assay, Lot #926230, may have become contaminated during filling. The particulates in the contamination may cause t

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.