Medical Device Recalls

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510(K) Number: K992368

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Product Description	Recall Class	FDA Recall Posting Date	Recalling Firm
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TufTex Embolectomy Catheter, Model No. This catheter has a latex balloon and a single lumen extr...	2	11/11/2022	FEI # 1220948 LeMaitre Vascular, Inc.
LeMaitre Single Lumen Embolectomy Catheter 5F, 80 cm, Model 1601-58 and e1601-58. Indicated for the...	2	12/04/2015	FEI # 1220948 LeMaitre Vascular, Inc.
LeMaitre Single Lumen Embolectomy Catheter 4F, 80 cm, Model 1601-48 and e1601-48. Indicated for the...	2	12/04/2015	FEI # 1220948 LeMaitre Vascular, Inc.
LeMaitre Single Lumen Embolectomy Catheter 3F, 80 cm, Model 1601-38 and e1601-38. Indicated for the ...	2	12/04/2015	FEI # 1220948 LeMaitre Vascular, Inc.
LeMaitre NovaSil Silicone Single Lumen Embolectomy Catheter 6F, 80 cm, Model 1601-68. Indicated for...	2	12/04/2015	FEI # 1220948 LeMaitre Vascular, Inc.
LeMaitre NovaSil Silicone Single Lumen Embolectomy Catheter 2F, 60 cm, Model e1801-26. Indicated fo...	2	12/04/2015	FEI # 1220948 LeMaitre Vascular, Inc.
LeMaitre Embolectomy Catheter 3F Single Lumen, Balloon volume 0.2ml, Length 80 cm, Latex Model: ...	2	02/24/2005	FEI # 1220948 Lemaitre Vascular, Inc.
LeMaitre Embolectomy Catheter 2F Single Lumen, Balloon Volume 0.05 ml, Length 60 cm. Latex Model:...	2	02/24/2005	FEI # 1220948 Lemaitre Vascular, Inc.
LeMaitre Embolectomy Catheter 5F Single Lumen, Balloon Volume 1.5 ml, Length 80 cm, Latex Model: ...	2	02/24/2005	FEI # 1220948 Lemaitre Vascular, Inc.