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Medline convenience kits containing semi-rigid suction… recallZ-3111-2024 · MEDLINE INDUSTRIES, LP - Northfield · initiated Jun 27, 2024

Open, Classified

Is my device affected?

  1. Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
  2. If yours is listed, follow the instructions from MEDLINE INDUSTRIES, LP - Northfield or your healthcare provider. The company's action is summarized under what the company is doing.
  3. Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.

Where to find your model and lot numbers · What recall classes and statuses mean

Why it was 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.

FDA root cause category: Process control

What the company is doing

Medline Industries issued a MEDICAL DEVICE RECALL notice to its consignees on 06/27/2024 via US mail and email. The notice explained the problem with the device, potential risk to the patient, and requested the consignee immediately check their stock for the affected item number and the affected lot numbers and destroy any affected inventory. Distributors were directed to notify their customers of the recall and request the affected products be destroyed. For questions: contact the Recall Department at 866-359-1704 or [email protected].

Recall details

Recall number
Z-3111-2024
Status
Open, Classified
Initiated by the company
Jun 27, 2024
Posted by the FDA
Sep 11, 2024
Recalling firm
MEDLINE INDUSTRIES, LP - Northfield
Quantity
6257 units
Product code
NWU
Distribution
Worldwide distribution - US Nationwide and the countries of Canada, Panama.

Product description

Medline convenience kits containing semi-rigid suction liners labeled as follows: a) ENDO BRONCH PACK, Pack Number DYKE1355; b) ENDO BASIC KIT, Pack Number DYKE1356; c) ENDOSCOPY KIT, Pack Number DYKE1771C

Code information (models, lots, serial numbers)

a) DYKE1355: UDI/DI case 40889942274193, UDI/DI each 10889942274192; Lot Numbers: 23LBB043, 24BBJ327, 24CBS751; b) DYKE1356: UDI/DI case 40889942274186, UDI/DI each 10889942274185; Lot Numbers: 23LBD062, 24ABA646, 24BBJ328, 24CBG449, 24DBE106, 24EBG238; c) DYKE1771C: UDI/DI case 40195327331994, UDI/DI each 10195327331993; Lot Numbers: 24ABX292

Devices named in this recall

3 devices in the FDA device registry whose identifier appears in the recall's code information.

Other products in the same recall event

The FDA groups related products into one recall event (event 95128).

Sources and updates

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