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Open, Classified

Medline convenience kits labeled as: a. MIDDLE EAR PACK-LF, Model DYNJ0689093V, b. EENT PACK, Model Number DYNJ62927 Model/Catalog Number: a. DYNJ0689093V, b. DYNJ62927

FDA Recall Z-1472-2022 · Posted None

Recalling FirmMEDLINE INDUSTRIES, LP - SPT
Recall StatusOpen, Classified
Product CodeOGR
Date Initiated2022-06-06
Product Quantity477 units

Reason for Recall

Kits contain leaking bottles of isopropyl alcohol

Firm Action

The firm's consignees were notified by US mail on 06/06/2022 and instructed to destroy any affected kits on hand in accordance with their local and state regulations.

Root Cause

Under Investigation by firm

Distribution Pattern

US Nationwide distribution.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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