FDAFDA · Food and drugs·Recall number Z-3120-2024
Medline convenience kits containing semi-rigid suction liners labeled as follows: a) AMB VITRECTOMY, Pack Number DYNJ59921B; b) AMB VITRECTOMY, Pack Number DYNJ59921BH; c) AMB OCULOPLASTICS MUSC, Pack Number DYNJ59923B; d) AMB OCULOPLASTICS MUSC, Pack Number DYNJ59923BH; e) AMB CUSTOM EYE, Pack Number DYNJ59924B; f) AMB CUSTOM EYE, Pack Number DYNJ59924BH; g) CATARACT-30843, Pack Number DYNJVB91139
Published September 18, 2024 · Recall initiated: June 27, 2024
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
XXX
What to do
Voluntary: Firm initiated · Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Recall details
- Manufacturer
- MEDLINE INDUSTRIES, LP - Northfield
- Distributor
- Worldwide distribution - US Nationwide and the countries of Canada, Panama.
- Lot
- a) DYNJ59921B: UDI/DI case 40195327037148, UDI/DI each 10195327037147, Lot Numbers: 23LBS025, 24ABY181; b) DYNJ59921BH: UDI/DI case 40195327037148, UDI/DI each 10195327037147, Lot Numbers: 23LBS025, 24ABY181; c) DYNJ59923B: UDI/DI case 40195327043217, UDI/DI each 10195327043216, Lot Numbers: 23LBF664, 23LBS053, 24ABY182; d) DYNJ59923BH: UDI/DI case 40195327043217, UDI/DI each 10195327043216, Lot Numbers: 23LBF664, 23LBS053, 24ABY182; e) DYNJ59924B: UDI/DI case 40195327036967, UDI/DI each 10195327036966, Lot Numbers: 23LBD909; f) DYNJ59924BH: UDI/DI case 40195327036967, UDI/DI each 10195327036966, Lot Numbers: 23LBD909; g) DYNJVB91139: UDI/DI case 40195327607105, UDI/DI each 10195327607104, Lot Numbers: 24CLA670, 24CLA895
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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