openFDA Device Enforcement
Report-date coverage
June 20, 2012–July 08, 2026
Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
openFDA Device Recall
event_date_initiated coverage
June 01, 1997–June 30, 2026
Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.
Product dates, classifications, firms, and source wording remain attached to their individual rows.
Opening this dossier never hides products that did not match a prior timeline filter.
device · product 1 of 2
Rusch Greenlite Single-Use Metal Laryngoscope Blade for Fiber Optic System
338,928 (199,018 US and 139,910 OUS) for all products
App-derived interpretation
Unknownreason.no_named_rule · v1.0.0
The products are being recalled due to reports of breakage broke at the point of a welded joint either prior to use during setup or during use inside the patient's mouth.
These labels are deterministic app interpretations, not FDA categories.
The products are being recalled due to reports of breakage broke at the point of a welded joint either prior to use during setup or during use inside the patient's mouth.
Code information
Product Code 004551003; Lot Numbers 1811331, 1902331, 1904331
Distribution pattern
Distributed nationwide in the US and to Puerto Rico; OUS to more than 20 countries; To the following government VA medical Centers: VAMC - KANSAS CITY MO 4801 E Linwood Blvd Kansas City MO 64128-2218
device · product 2 of 2
Rusch Greenlite Single-Use Metal Laryngoscope Blade for Fiber Optic System
338,928 (199,018 US and 139,910 OUS) for all products
App-derived interpretation
Unknownreason.no_named_rule · v1.0.0
The products are being recalled due to reports of breakage broke at the point of a welded joint either prior to use during setup or during use inside the patient's mouth.
These labels are deterministic app interpretations, not FDA categories.
The products are being recalled due to reports of breakage broke at the point of a welded joint either prior to use during setup or during use inside the patient's mouth.
Code information
Product Code 004551004; Lot Numbers 1812341, 1903341
Distribution pattern
Distributed nationwide in the US and to Puerto Rico; OUS to more than 20 countries; To the following government VA medical Centers: VAMC - KANSAS CITY MO 4801 E Linwood Blvd Kansas City MO 64128-2218
