Unapproved design changes to the products outside of the 510(k) clearance.
Reason for recall: Unapproved design changes to the products outside of the 510(k) clearance. Distribution: Worldwide distribution - US Nationwide and the countries of Canada, Panama, Barbados. Quantity: 270,311 total Lot/code info: DYNJ35056A UDI-DI 10889942227563 (EA) 40889942227564 (CS) LOT 24ABN639 DYNJ69318A UDI-DI 10195327370756 (EA) 40195327370757 (CS) LOTS 23DMD456 23EMB847 23HMB969 23IMC364 23JME011 23JMI841 23LMC384 24BMD333 24CMB768 24CMJ586 24EMJ527 24GMD970 24JMB408 24JMI594 24KMC774 ***Updated 5/20/26 - The following lots were included in the customer letter but not the FDA submission.*** DYNJ69318A lots 23FMA845 23FMA924 25BMF603
10889942227563, 40889942227564, 10195327370756, 40195327370757
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.