PlainRecalls
FDA Devices Moderate Class II Ongoing

Medline convenience kits containing semi-rigid suction liners labeled as follows: MERCY TIFFIN C-SECTION, Pack Number DYNJ909732

Reported: September 18, 2024 Initiated: June 27, 2024 #Z-3119-2024

Product Description

Medline convenience kits containing semi-rigid suction liners labeled as follows: MERCY TIFFIN C-SECTION, Pack Number DYNJ909732

Reason for Recall

Due to reported adverse events, Medline Industries, LP. is issuing a recall on specific SKUs and lots of 1500 cc semi-rigid liners manufactured from 09/2023-11/2023 due to the potential loss of suction or low suction during intermittent suction use.

Details

Units Affected
35 units
Distribution
Worldwide distribution - US Nationwide and the countries of Canada, Panama.
Location
Northfield, IL

Frequently Asked Questions

What product was recalled?
Medline convenience kits containing semi-rigid suction liners labeled as follows: MERCY TIFFIN C-SECTION, Pack Number DYNJ909732. Recalled by MEDLINE INDUSTRIES, LP - Northfield. Units affected: 35 units.
Why was this product recalled?
Due to reported adverse events, Medline Industries, LP. is issuing a recall on specific SKUs and lots of 1500 cc semi-rigid liners manufactured from 09/2023-11/2023 due to the potential loss of suction or low suction during intermittent suction use.
Which agency issued this recall?
This recall was issued by the FDA Devices on September 18, 2024. Severity: Moderate. Recall number: Z-3119-2024.