PlainRecalls
FDA Devices Moderate Class II Ongoing

Medline medical procedure kits labeled as follows: a) KIT CANISTER SUCT W 12FT, REF DYKM2169

Reported: August 28, 2024 Initiated: March 22, 2024 #Z-2709-2024

Product Description

Medline medical procedure kits labeled as follows: a) KIT CANISTER SUCT W 12FT, REF DYKM2169

Reason for Recall

A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.

Details

Units Affected
1700 units
Distribution
Worldwide - US Nationwide and the countries of Panama, Mexico, Canada, Qatar, El Salvador, Oman, Colombia, Singapore.
Location
Northfield, IL

Frequently Asked Questions

What product was recalled?
Medline medical procedure kits labeled as follows: a) KIT CANISTER SUCT W 12FT, REF DYKM2169. Recalled by MEDLINE INDUSTRIES, LP - Northfield. Units affected: 1700 units.
Why was this product recalled?
A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
Which agency issued this recall?
This recall was issued by the FDA Devices on August 28, 2024. Severity: Moderate. Recall number: Z-2709-2024.