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    CDI OneView System BPM Probe: Cat. No. CDI753 - CDI OneView BPM Probe, Cat. No. CDI753TK - CDI OneView BPM Probe Trial Kit

    FDA Recall
    Open, Classified ·Terumo Cardiovascular Systems Corporation·Product code DRY·May 28, 2025

    GentleWave System APM Procedure Instrument with Matrix REF GW-APM-PI02

    FDA Recall
    Open, Classified ·Sonendo Inc·Product code ELC·October 14, 2022

    Fuse ULTRA Foot Plating System Instructions for Use. Models: OS200400, OS200401, OS328017, OS200020L, OS200025L, OS200120L, OS200125, OS200125L, OS200135, OS200324, OS200325, OS200326, OS328026, OS328028C, OS216150, OS218150, OS292110, OS292120, OS292160, OS292200, OS200516, OS200518, OS200520, OS200522, OS200616, OS200618, OS200620, OS200622, OS421300, OS421302, OS421304, OS421306, OS421308, OS421208, OS421210, OS421212, OS421000L, OS421000R, OS421002L, OS421002R, OS421004L, OS421004R, OS421006L, OS421006R, OS42260LL, OS42260LR, OS42260ML, OS42260MR, OS42260SL, OS42260SR, OS42260XSL, OS42260XSR, OS422800, OS422803, OS422804, OS422805, OS422807, OS422825, OS422400, OS422403, OS422404, OS422405, OS422406, OS422407, OS421406, OS421408, OS421414, OS422702, OS422703, OS422712, OS422714, OS422716, OS421512, OS421514, OS421516, OS421112, OS421116, OS421120, OS421124, OS421130, OS42150L, OS42150M, OS42150S, OS42150XS, OS326920-T, OS326922-T, OS326924-T, OS326925, OS326925-T, OS326926-T, OS326928, OS326928-T, OS326930, OS326930-T, OS326932, OS326932-T, OS326934, OS326934-T, OS326936, OS326936-T, OS326938, OS326938-T, OS326940, OS326940-T, OS326945, OS326945-T, OS326950, OS326950-T, OS326955, OS326955-T, OS326960, OS326960-T, OS327920, OS327922, OS327924, OS327926, OS327928, OS327930, OS327932, OS327934, OS327936, OS327938, OS327940, OS327945, OS327950, OS327955, OS327960, OS421710, OS421712, OS421714, OS421716, OS421718, OS421720, OS421722, OS421724, OS421726, OS421728, OS421730, OS421735, OS421740, OS421745, OS421750, OS422508, OS422510, OS422512, OS422514, OS422516, OS422518, OS422520, OS422522, OS422524, OS422526, OS422528, OS422530, OS421814, OS421816, OS421818, OS421820, OS421822, OS421824, OS421826, OS421828, OS421830, OS421835, OS421840, OS421845, OS421850, OS422608, OS422610, OS422612, OS422614, OS422616, OS422618, OS422620, OS422622, OS422624, OS422626, OS422628, OS422630, R327924, R327928, R327932, R327936, R327940, R327945, R327950, R421000L, R421000R, R421710, R421712, R421714, R421716, R421718, R421720, R421722, R421724, R421726, R421728, R421730, R421735, R421740, R421814, R421816, R421818, R421820, R421822, R421824, R421826, R421828, R421830, R421835, R421840, R421845, R421850, R42260ML, R42260MR, R42260SL, R42260SR, R42260XSL, R42260XSR

    FDA Recall
    Open, Classified ·CPM Medical Consultants, LLC.·Product code HRS·September 17, 2025

    Recreo Hair Growth Laser Comb

    FDA Recall
    Open, Classified ·OMM Imports, Inc. dba Zero Gravity·Product code OAP·September 1, 2022

    Infant Heel Warmers w/strap, Reference # 989805603201 1223

    FDA Recall
    Open, Classified ·Philips North America Llc·Product code IMD·November 29, 2021

    Cardinal Infant Heel Warmer, Reference # 989805617251 11470-010T

    FDA Recall
    Open, Classified ·Philips North America Llc·Product code IMD·November 29, 2021

    Heel Snuggler, Reference # 989805603411 99047

    FDA Recall
    Open, Classified ·Philips North America Llc·Product code MPO·November 29, 2021

    Medichoice Infant Heel Warmer, Reference # 989805643721 1079906

    FDA Recall
    Open, Classified ·Philips North America Llc·Product code IMD·November 29, 2021

    Infa-Therm Transport Mattress, Reference Number 989805616831 1015

    FDA Recall
    Open, Classified ·Philips North America Llc·Product code IMD·November 26, 2021

    PowerPort isp M.R.I. Implantable Port with Attachable 8F Polyurethane Open-Ended Single-Lumen Venous Catheter

    FDA Recall
    Open, Classified ·Bard Peripheral Vascular Inc·Product code LJT·February 14, 2019

    Biofinity Toric Multifocal Contact Lens

    FDA Recall
    Open, Classified ·CooperVision, Inc.·Product code LPM·June 16, 2025

    BIOFINITY XR TORIC Lenses - Soft Contact lenses Indicated for the correction of ametropia (myopia or hyperopia with astigmatism) with presbyopia in aphakic and non-aphakic persons.

    FDA Recall
    Open, Classified ·CooperVision, Inc.·Product code LPM·August 29, 2024

    Biofinity XR Toric 6-pack- Soft (hydrophilic) Contact Lens (extended wear)

    FDA Recall
    Open, Classified ·CooperVision, Inc.·Product code LPM·January 26, 2023

    Biofinity XR Toric Single Diagnostic lens- Soft (hydrophilic) Contact Lens (extended wear)

    FDA Recall
    Open, Classified ·CooperVision, Inc.·Product code LPM·January 26, 2023

    Biofinity XR Toric Contact Lens

    FDA Recall
    Open, Classified ·CooperVision, Inc.·Product code LPM·June 16, 2025

    Alpha Interlock Suspension System Lanyard Body: An external prosthetic device. The Alpha Lanyard includes suction with a one-way air expulsion valve plus a locking mechanism. Product design features an easy release mechanism. Available with or without a titanium pyramid. The lanyard is part of the Alpha Interlock" Suspension System. This system allows you to interchange suspension methods without remaking a socket Model, 3 part numbers - 700-AIS100, Alpha Interlock Suspension System with Alpha Lanyard - 700-AIS101, Alpha Interlock Suspension System with Alpha Lanyard w/Titanium Pyramid - 700-AIS107, Alpha Interlock Suspension System Lanyard Body ONLY

    FDA Recall
    Open, Classified ·WillowWood Global Llc·Product code IPM·April 20, 2021

    NuOss Collagen Block Size 8mm x 9mm x 9mm- used in filling periodontal and maxillofacial defects. Catalog Number: 5099250

    FDA Recall
    Open, Classified ·Ace Surgical Supply Co., Inc.·Product code NPM·February 2, 2022

    Biofinity Toric Multifocal Lenses - Soft Contact lenses Indicated for the correction of ametropia (myopia or hyperopia with astigmatism) with presbyopia in aphakic and non-aphakic persons.

    FDA Recall
    Open, Classified ·CooperVision, Inc.·Product code LPM·August 29, 2024