RegWardenFDA facility compliance records
Recall

Class II — Corin Ltd

Recalling firmCorin Group
Registered facilityView this company's 4 registered facilities → (openFDA recall records do not name a specific facility)
ClassificationClass II
StatusOngoing
ReasonThe BIOLOX Delta Ceramic Head size 36XL is labelled as the size 32XL and vice-versa.
ProductCorin BIOLOX DELTA MOD HEAD, 036mm EX LONG +8mm, REF 104.3615
Quantity12 units
DistributionUS Nationwide distribution in the states of FL, GA, MA, MI, Ok, PA, TX.
Initiated2022-11-08
Classified2022-12-19
Recall numberZ-0727-2023
InitiationVoluntary: Firm initiated

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Class II recall — Corin Ltd (Z-0727-2023).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/91183/

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