(1) Arrow¿ STIM CPNB TUOHY NDL: 18G x 14CM (5-1/2") AB-18140-N (2) Arrow¿ STIM CPNB TUOHY NDL: ...
FDA Recall #Z-1253-2020 — Class II — December 20, 2019
Product Description
(1) Arrow¿ STIM CPNB TUOHY NDL: 18G x 14CM (5-1/2") AB-18140-N (2) Arrow¿ STIM CPNB TUOHY NDL: 18G x 11CM (4-3/8") AB-18110-N (3) Arrow¿ STIM CPNB TUOHY NDL: 18G x 8CM (3-1/8") AB-18080-N (4) Arrow¿ STIM CPNB TUOHY NDL: 17G x 8CM (3-1/8") AB-17080-N (5) Arrow¿ STIM CPNB TUOHY NDL: 17G x 14CM (5-1/2") AB-17140-N (6) Arrow¿ INSL CPNB TUOHY NDL: 17G x 15CM (6") AB-00150 (7) Arrow¿ STIM CPNB TUOHY NDL: 17G x 11CM (4-3/8") AB-17110-N
Reason for Recall
Product lidstock contains the incorrect expiration date for the product
Recalling Firm
Arrow International Inc — Reading, PA
Classification
Class II — May cause temporary or medically reversible adverse health consequences.
Product Type
Devices
Product Quantity
2126
Distribution
Nationwide Foreign: AT, AU, DE, CA, CZ, GT, NZ, PL, SK, and ZA
Code Information
Lot Number: (1) AB-00150 13F16B0155; (2) AB-17080-N 13F18J0654, 13F16H0046,13F16F0210, 13F16E0106, 13F16C0107; (3) AB-17110-N 13F16G0226, 13R16G0226, 13F16F0079; (4) AB-17140-N 13F16F0190, 13F16C0045; (5) AB-18080-N 13F16H0048, 13F16F0007, 13F16B0181, (6) AB-18110-N 13F16F0189, 13F16C0046; (7) AB-18140-N 13F16H0292;
Status
Terminated
Voluntary / Mandated
Voluntary: Firm initiated