- Recalling firm
- Cook Incorporated
- Reason for recall
- Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
- Affected products (lot / model / serial)
- Reference Part Number C-UTPTY-1400-WAYNE-112497-IMH, UDI (01)00827002565371(17)261020(10)15719344X, Lot Number 15719344X; Reference Part Number C-UTPTY-1400-WAYNE-112497-IM , UDI (01)00827002565371(17)261018(10)15714808X, Lot Number 15714808X; Reference Part Number C-UTPTY-1400-WAYNE-112497-IMH, UDI (01)00827002565371(17)260115(10)15834145, Lot Number 15834145; Reference Part Number C-UTPTY-1400-WAYNE-112497-IMH, UDI (01)00827002565371(17)260115(10)15834147, Lot Number 15834147.
- Units affected
- 318 units
- Distribution pattern
- Worldwide distribution.
- Firm location
- Bloomington, IN, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-1792-2026
- Recall initiated
- March 5, 2026
- FDA classification date
- April 6, 2026
- FDA report date
- April 15, 2026
- FDA event ID
- 98495
- Last updated on HTM Vibe
- July 24, 2026