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
SCISSORS, OR, SHARP/BLUNT, 5.5", STERILE, Item Number DYND04000
The 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.
Code information
DYND04000, UDI-DI: 10193489191349(each), 20193489191346(case), Lot Number: 2023102590
Distribution pattern
US Nationwide distribution in the states CA, CO, IL, KS, and MI.
device · product 2 of 2
FORCEP, STD STR, STERILE KELLY, 5.5 IN, Item Number DYNJ04048
The 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.
Code information
DYNJ04048, UDI-DI: 10193489195248(each), 20193489195245(case), Lot Number: 2023112290
Distribution pattern
US Nationwide distribution in the states CA, CO, IL, KS, and MI.
