- 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-CSRC-7.5D-40-STRANGE, UDI (01)00827002091085(17)260221(10)15133690X, Lot Number 15133690X; Reference Part Number C-CSRC-7.5D-40-STRANGE, UDI (01)00827002091085(17)260314(10)15274382, Lot Number 15274382; Reference Part Number C-CSRC-7.5D-40-STRANGE, UDI (01)00827002091085(17)270104(10)15435573, Lot Number 15435573; Reference Part Number C-CSRC-7.5D-40-STRANGE, UDI (01)00827002091085(17)270118(10)15445615, Lot Number 15445615; Reference Part Number C-CSRC-7.5D-40-STRANGE, UDI (01)00827002091085(17)270104(10)15501690, Lot Number 15501690.
- Units affected
- 49 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-1784-2026
- 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