FDA Device Intelligence
HomeMEDTRONIC MINIMED, INC. › Extended™ Reservoir 3.0mL

Extended™ Reservoir 3.0mL

MEDTRONIC MINIMED, INC. · Model MMT-342G · UDI-DI 00763000837211

LZP Prescription
1
510(k) clearances
2,822
Adverse events (1 deaths)
25
Recalls
24
Facilities

Description

RSVR MMT-342G 5PK EW 3ML US

Recalls

DateFirmReason
2026-07-31Johnson & Johnson Surgical Vision, Inc.Surgical instructions sent for viscoelastic products used during ophthalmic viscosurgical cataract procedures including in part: If resistance is encountered during insertion, with
2019-12-03Johnson & Johnson Surgical Vision IncOphthalmic viscosurgical device may be difficult to remove from the eye, leading to increased postoperative intraocular pressure requiring additional intervention. Also, reports of
2017-04-01Abbott Medical Optics Inc. (AMO)Remote possibility that certain solutions in these lots may contain microscopic glass particles due to damage that occurred at the cylinder neck during the manufacturing process.
2017-04-01Abbott Medical Optics Inc. (AMO)Remote possibility that certain solutions in these lots may contain microscopic glass particles due to damage that occurred at the cylinder neck during the manufacturing process.
2017-04-01Abbott Medical Optics Inc. (AMO)Remote possibility that certain solutions in these lots may contain microscopic glass particles due to damage that occurred at the cylinder neck during the manufacturing process.
2017-04-01Abbott Medical Optics Inc. (AMO)Remote possibility that certain solutions in these lots may contain microscopic glass particles due to damage that occurred at the cylinder neck during the manufacturing process.
2017-04-01Abbott Medical Optics Inc. (AMO)Remote possibility that certain solutions in these lots may contain microscopic glass particles due to damage that occurred at the cylinder neck during the manufacturing process.
2017-04-01Abbott Medical Optics Inc. (AMO)Remote possibility that certain solutions in these lots may contain microscopic glass particles due to damage that occurred at the cylinder neck during the manufacturing process.
2014-11-06Abbott Medical Optics Inc (AMO)AMO has received complaints where the finger grip dislodged while depressing the syringe plunger. The finger grip dislodgement could result in the surgeon's hand unintentionally m
2013-11-25C.L.R. Medicals International, Inc.CLR Medicals International Inc., initiated a nationwide recall of Viscocel and Viscocel Plus, in response to FDA inspection findings of deficiencies in the Quality System Regulatio

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.