Reported Sep 18, 2024 · Ongoing

Medline convenience kits containing semi-rigid suction liners labeled as follows

MEDLINE INDUSTRIES, LP - Northfield

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: MEDLINE INDUSTRIES, LP - Northfield · 3 Lakes Dr · Northfield, IL · 60093-2753

Is this the product you have?

Medline convenience kits containing semi-rigid suction liners labeled as follows

7 of 7 products

Products covered by this recall
#Product as published
1AMB VITRECTOMY, Pack Number DYNJ59921B
2AMB VITRECTOMY, Pack Number DYNJ59921BH
3AMB OCULOPLASTICS MUSC, Pack Number DYNJ59923B
4AMB OCULOPLASTICS MUSC, Pack Number DYNJ59923BH
5AMB CUSTOM EYE, Pack Number DYNJ59924B
6AMB CUSTOM EYE, Pack Number DYNJ59924BH
7CATARACT-30843, Pack Number DYNJVB91139
Lot codes and dates

7 of 7 products

Products covered by this recall
#BarcodesProduct as published
14019532703714810195327037147UDI/DI case 40195327037148, UDI/DI each 10195327037147, Lot Numbers: 23LBS025, 24ABY181
24019532703714810195327037147DYNJ59921BH: UDI/DI case 40195327037148, UDI/DI each 10195327037147, Lot Numbers: 23LBS025, 24ABY181
34019532704321710195327043216DYNJ59923B: UDI/DI case 40195327043217, UDI/DI each 10195327043216, Lot Numbers: 23LBF664, 23LBS053, 24ABY182
44019532704321710195327043216DYNJ59923BH: UDI/DI case 40195327043217, UDI/DI each 10195327043216, Lot Numbers: 23LBF664, 23LBS053, 24ABY182
54019532703696710195327036966DYNJ59924B: UDI/DI case 40195327036967, UDI/DI each 10195327036966, Lot Numbers: 23LBD909
64019532703696710195327036966DYNJ59924BH: UDI/DI case 40195327036967, UDI/DI each 10195327036966, Lot Numbers: 23LBD909
74019532760710510195327607104DYNJVB91139: UDI/DI case 40195327607105, UDI/DI each 10195327607104, Lot Numbers: 24CLA670, 24CLA895
Amount recalled
720 units

This recall covers 106 products

The agency filed one notice per product. You are reading one of them; the other 105 are below.

93 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

XXX

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 6:23 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.