Arrowhead DE LLC recalls
1 recall filed under Arrowhead DE LLC. The most recent was published August 26, 2026.
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Class II · 2 months ago
Arrowhead DE LLC Arrow-LOK Implant, REF: 21-253519, 21-253522, 21-253525 recall: Implant did not undergo required gamma radiation dose audit. A potential
Implant did not undergo required gamma radiation dose audit. A potential reduction in sterility assurance could lead to patient infection.
About this page
Arrowhead DE LLC appears here because a federal agency named it as the recalling firm or the brand on the label. A recall is not a judgement about everything the company sells — it covers only the lot codes and models listed in each notice.