Recall Z-0538-2026

Polymedco, Inc. / Polymedco Cancer Diagnostic Products, LLC · initiated October 6, 2025

Class III Open, Classified

Class III – products unlikely to cause any adverse health reaction but that violate FDA labeling or manufacturing laws

Product

OC-Auto FOBT-CHEK Negative Controls is the negative hemoglobin control materials designed to monitor FOBT (Fecal Occult Blood Test)

Codes / lots: UDI: 00855574005520, Catalog Number(s): OCQN Lot Number(s): Lot 250805

Reason for recall

A labeling error was identified on the affected product. The expiration date on the kit box label and on the vial labels incorrectly stated the expiration date as 2026-01-16. The correct expiration date should be 2027-01-17.

FDA-determined cause: Process control

Action taken

On October 6, 2025 URGENT PRODUCT RECALL: INCORRECT EXPIRATION DATE ON PRODUCT LABELING letters were sent to customers. ACTIONS REQUIRED BY YOU 1. Please trace the OCQN kits, lot 250805 in your inventory and at the customer sites listed in appendix one. If the kits have already been used no further action is required. There is no risk to patient care. 2. For customers with remaining stock there are two options:1) Manually correct the date on the packaging and vial labels to 2027-01-17 and add this notification to the kit box. OR 2) Request replacement stock with corrected labeling from Polymedco. ADDITIONAL INFORMATION Polymedco s inventory of Lot 250805 has been updated with new labels with the correct shelf life. All kits provided from September 25, 2025, will have the correct expiration date.

Details

Recall number
Z-0538-2026
Initiated
October 6, 2025
Posted by FDA
November 17, 2025
Product code
JJY – Multi-Analyte Controls, All Kinds (Assayed)
Quantity
403 units
Distribution
USA: AK AL,AR,AZ, CA,CO,CT,DC,DE,FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MO, MT, NC, NE, NH, NJ, NM, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, ,WI, WV, WY, Canada: AB, ON
Recalling firm
Polymedco, Inc. / Polymedco Cancer Diagnostic Products, LLC, Cortlandt Manor, NY

Official FDA recall record