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Devices
Device Recall Peregrine 20 GA Endo Ocular Adjustable Laser Probe (Smart Flex)
Model / Serial
Device numbers: PD720.50, PD720.52, PD723.50, PD723.52, PD725.50, PD725.52. Lot numbers 926287, 937391, 931335, 933355, 935370, 937390, 940422, 916188, 917184, 919211, 920228, 922244, 925269, 916189, 917185, 919216, 920229, 923245, 925272, 952026, 002048, 005069, 916186, 918196, 919205, 920240, 924268, 926285, 916184, 918203, 919208, and 922239.
Product Classification
Ophthalmic Devices
Device Class
2
Implanted device?
No
Distribution
Product was distributed to hospitals and eye surgery centers in Florida, Maryland, Missouri, North Carolina, Ohio, Pennsylvania, Texas.
Product Description
Peregrine 20 GA Endo Ocular Adjustable Laser Probe
Manufacturer
Peregrine Surgical Ltd
1 Event
Recall of Device Recall Peregrine 20 GA Endo Ocular Adjustable Laser Probe (Smart Flex)
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Manufacturer
Peregrine Surgical Ltd
Manufacturer Address
Peregrine Surgical Ltd, 51 Britain Dr, New Britain PA 18901-5186
Manufacturer Parent Company (2017)
Peregrine Surgical Ltd.
Source
USFDA
Language
English
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