LeMaitre 5F Plus Over the Wire Embolectomy Catheter recall
LeMaitre 5F Plus Over the Wire Embolectomy Catheter, Model Nos. 1651-84, e1651-84, 1651-88, e1651-88. The LeMaitre Over the Wire Embolectomy Catheter…
Why was LeMaitre 5F Plus Over the Wire Embolectomy Catheter recalled?
There has been an increased trend in reports of catheters failing to deflate during use, which may ultimately lead to tip separation.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
OTW2897¿ OTW3273¿ OTW3333¿ OTW3379¿ OTW3418¿ OTW3543¿ OTW3564¿ OTW3620¿ OTW3700¿ OTW3740¿ OTW3758¿ OTW3805¿ OTW3865¿ OTW3879¿ OTW3892¿ OTW3966¿ OTW4009¿ OTW4010¿ OTW4017¿ OTW4018¿ OTW4024¿ OTW4060¿ OTW4063¿ OTW4064¿ OTW4065¿ OTW4117¿ OTW4201¿ OTW4238¿ OTW4239¿ OTW2957¿ OTW3001¿ OTW3266¿ OTW3395¿ OTW3565¿ OTW3637¿ OTW3638¿ OTW3658¿ OTW3665¿ OTW3670¿ OTW3671¿ OTW3682¿ OTW3683¿ OTW3694¿ OTW3695¿ OTW3701¿ OTW3708¿ OTW3727¿ OTW3728¿ OTW3747¿ OTW3769¿ OTW3770¿ OTW3775¿ OTW3776¿ OTW3779¿ OTW3780¿ OTW3810¿ OTW3820¿ OTW3821¿ OTW3853¿ OTW3854¿ OTW3880¿ OTW3881¿ OTW3886¿ OTW3893¿ OTW3898¿ OTW3899¿ OTW3915¿ OTW3916¿ OTW3924¿ OTW3930¿ OTW3957¿ OTW3958¿ OTW3981¿ OTW3982¿ OTW4011¿ OTW4025¿ OTW4026¿ OTW4030¿ OTW4031¿ OTW4052¿ OTW4053¿ OTW4054¿ OTW4066¿ OTW4067¿ OTW4068¿ OTW4073¿ OTW4074¿ OTW4075¿ OTW4092¿ OTW4093¿ OTW4098¿ OTW4099¿ OTW4105¿ OTW4106¿ OTW4107¿ OTW4119¿ OTW4120¿ OTW4157¿ OTW4158¿ OTW4188¿ OTW4197¿ OTW4220¿ OTW4221¿ OTW4222¿ OTW4229¿ OTW4230¿ OTW4247¿ OTW4249¿ OTW4254¿ OTW4255¿ OTW4258¿ OTW4259¿ OTW4260¿ OTW4261¿ OTW4263¿ OTW4291¿ OTW4294¿ OTW4339¿ OTW4341¿ OTW4363¿ OTW4364¿ OTW2942¿ OTW2959¿ OTW2987¿ OTW3207¿ OTW3292¿ OTW3303¿ OTW3312¿ OTW3322¿ OTW3323¿ OTW3351¿ OTW3367¿ OTW3438A¿ OTW3511¿ OTW3635¿ OTW3636¿ OTW3660¿ OTW3661¿ OTW3667¿ OTW3688¿ OTW3689¿ OTW3706¿ OTW3707¿ OTW3711¿ OTW3717¿ OTW3718¿ OTW3734¿ OTW3750¿ OTW3783¿ OTW3784¿ OTW3794¿ OTW3795¿ OTW3827¿ OTW3828¿ OTW3851¿ OTW3852¿ OTW3862¿ OTW3863¿ OTW3882¿ OTW3896¿ OTW3897¿ OTW3907¿ OTW3908¿ OTW3931¿ OTW3936¿ OTW3944¿ OTW3945¿ OTW3962¿ OTW3963¿ OTW3978¿ OTW3979¿ OTW3995¿ OTW3996¿ OTW4033¿ OTW4034¿ OTW4057¿ OTW4058¿ OTW4084¿ OTW4085¿ OTW4127¿ OTW4128¿ OTW4140¿ OTW4141¿ OTW4146¿ OTW4147¿ OTW4176¿ OTW4177¿ OTW4183¿ OTW4184¿ OTW4191¿ OTW4192¿ OTW4193¿ OTW4232¿ OTW4317¿ OTW4336¿ OTW2872¿ OTW3191¿ OTW3439¿ OTW3537¿ OTW3623¿ OTW3662¿ OTW3668¿ OTW3669¿ OTW3690¿ OTW3691¿ OTW3712¿ OTW3735¿ OTW3766¿ OTW3771¿ OTW3812¿ OTW3822¿ OTW3823¿ OTW3836¿ OTW3849¿ OTW3850¿ OTW3874¿ OTW3888¿ OTW3903¿ OTW3925¿ OTW3932¿ OTW3946¿ OTW3947¿ OTW3968¿ OTW3969¿ OTW3987¿ OTW3988¿ OTW4020¿ OTW4021¿ OTW4036¿ OTW4037¿ OTW4038¿ OTW4079¿ OTW4080¿ OTW4087¿ OTW4196¿ OTW4267¿ OTW4268¿ OTW4269¿ OTW4270¿ OTW4275¿ OTW4276¿ OTW4277¿ OTW4288¿ ***Added 3/19/20*** OTW2847¿ OTW2863¿ OTW2871¿ ***Updated 4/14/20*** The firm noted upon review that some of the original recall lots were originally relabeled with different lot numbers for Non-US customers. Those additional lot numbers are as follow: OTW3461 OTW3501 OTW3591 OTW3628 OTW3737 OTW3742 OTW3753 OTW3813 OTW3859 OTW3861 OTW4208 ***Updated 8/21/20*** Lots OTW4180, OTW4187, OTW4198, OTW4202, OTW4218, OTW4246
- Product
- LeMaitre 5F Plus Over the Wire Embolectomy Catheter, Model Nos. 1651-84, e1651-84, 1651-88, e1651-88. The LeMaitre Over the Wire Embolectomy Catheter…
- Recalling firm
- LeMaitre Vascular, Inc.
- Quantity
- 43315
- Distribution
- Worldwide distribution: US (Nationwide distribution) and foreign countries of: Australia, Austria, Belgium, Bulgaria, Colombia, Costa Rica, Czech Republic, Dominican Republic, Egypt, El Salvador, Estonia, Finland, France, Germany, Georgia, Hungary, Ireland, Israel, Italy, Japan, Korea, Netherlands, New Zealand, Norway, Poland, Portugal, Qatar, Saudi Arabia, Singapore, Slovenia, South Africa, Spain, Sweden, Switzerland, Taiwan, Thailand, United Kingdom, and Vietnam.
- Recall date
- April 8, 2020
- Classification
- Class I
- Status
- Ongoing
- Agency
- FDA (device)