Recall Z-0604-2024

Abbott Laboratories · initiated October 19, 2023

Class II Open, Classified

Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature

Product

Abbott CELL-DYN Ruby, Model CD-Ruby, List number 08H67-01, and Abbott CELL-DYN Sapphire, Model CD Sapphire, list number 08H00-01. Multi-parameter, automated hematology analyzer.

Codes / lots: All serial numbers are involved. CELL-DYN Ruby - UDI/DI 00380740017170; CELL-DYN Sapphire - UDI/DI 00380740016616.

Reason for recall

The devices contain a dry natural rubber (latex) subcomponent, which are not labeled as containing dry natural rubber(latex).

FDA-determined cause: Under Investigation by firm

Action taken

The recalling firm issued the Product Correction letter dated 10/19/2023 via FedEx priority overnight express delivery in the U.S. and either in person or mail, telephone, email, or FAX to the OUS consignees. The product correction is for instruments distributed in the U.S. and Brazil only. The letter explains the issue, lists all products involved (some of which have different 806 report numbers and are being submitted by Division III) and that a precautionary label indicating the presence of dry natural rubber (latex) will be applied to the devices by the local Abbott representative. The Impact to User Safety is provided and actions to be taken by the customer, which included: Follow good laboratory practice by wearing impervious gloves and other personal protective equipment when working on the listed Abbott products; complete and return the Customer Reply Form; if the consignee has forwarded the product(s) listed to other laboratories, inform them of this Product Correction and provide a copy of the letter; and retain this letter for their laboratory records.

Details

Recall number
Z-0604-2024
Initiated
October 19, 2023
Posted by FDA
December 21, 2023
Product code
GKZ – Counter, Differential Cell
Quantity
670 devices (329 US and 341 OUS)
Distribution
Distribution was made to AL, AR, AZ, CA, CO, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, NC, NE, NJ, NV, NY, OH, OK, PA, SC, SD, TN, TX, UT, VA, WA, WI, WV, and WY, including Puerto Rico. There was also government and military distribution. Foreign distribution was made to Brazil.
Recalling firm
Abbott Laboratories, Abbott Park, IL

Official FDA recall record