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Z-0266-2023 Class II

Recalled by Allison Medical, Inc. — Littleton, CO

FDA device recall Z-0266-2023 was initiated by Allison Medical, Inc. on January 19, 2018 and is designated Class II. Reason for recall: Insulin syringe retail packages incorrectly labeled as "Short Needle". Affected quantity: 1,500 Boxes (150,000 syringes).

Recall Details

Product Type: Devices
Report Date: November 30, 2022
Initiation Date: January 19, 2018
Termination Date: N/A
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 1,500 Boxes (150,000 syringes)

Product Description

InControl Insulin Syringes, Short Needle, 29 Gauge, 1CC

Reason for Recall

Insulin syringe retail packages incorrectly labeled as "Short Needle".

Distribution Pattern

Texas

Code Information

UDI/Lot/Expiration: 00041220791484/ 170407/ 2022-03-31