Medical DeviceOct 9, 2019
CooperSurgical Embryology Heated Plate within the RI Witness, Model Numbers 6-70-807 recall — FDA Z-0029-2020
The touchpad may not work properly after cleaning.
Class IIIFDA: TerminatedCooperSurgical, Inc.
October 2019 recalls — page 15
These records include useful source details for the selected month.
Medical DeviceOct 9, 2019
Medtronic Vascular SHERPA NX ACTIVE GUIDING CATHETER, 6F SAL1.0, .070", REF SA6SAL10. for recall — FDA Z-2671-2019
There is a potential for extensive loss of primary segment material exposing underlying stainless-steel braid wires on a subset of 6F Sherpa catheters.
Class IFDA: CompletedMedtronic Vascular
Medical DeviceOct 9, 2019
Medtronic Vascular SHERPA NX ACTIVE GUIDING CATHETER, 6F, JCR4.0, 100CM, 070", REF SA6JCR40. recall — FDA Z-2587-2019
There is a potential for extensive loss of primary segment material exposing underlying stainless-steel braid wires on a subset of 6F Sherpa catheters.
Class IFDA: CompletedMedtronic Vascular
Medical DeviceOct 9, 2019
Medtronic Vascular SHERPA NX ACTIVE GUIDING CATHETER, 6F ERAD RIGHT, .070", REF SA6ERADR. recall — FDA Z-2724-2019
There is a potential for extensive loss of primary segment material exposing underlying stainless-steel braid wires on a subset of 6F Sherpa catheters.
Class IFDA: CompletedMedtronic Vascular
Medical DeviceOct 9, 2019
Implant Direct Sybron Manufacturing ImplantDirect Legacy 3 Implant, REF 855216, SBM implant recall — FDA Z-0018-2020
Two units in distribution were found to be mislabeled on the vial cap with the incorrect part number.
Class IIFDA: TerminatedImplant Direct Sybron Manufacturing, LLC
Medical DeviceOct 9, 2019
Medtronic Vascular SHERPA NX ACTIVE GUIDING CATHETER, 6F, CHAMP0.5 SH, 100CM.070", REF recall — FDA Z-2574-2019
There is a potential for extensive loss of primary segment material exposing underlying stainless-steel braid wires on a subset of 6F Sherpa catheters.
Class IFDA: CompletedMedtronic Vascular
Medical DeviceOct 9, 2019
Medtronic Vascular SHERPA NX ACTIVE GUIDING CATHETER, 6F CHAMP1.5, .070", REF SA6CHAMP15. recall — FDA Z-2691-2019
There is a potential for extensive loss of primary segment material exposing underlying stainless-steel braid wires on a subset of 6F Sherpa catheters.
Class IFDA: CompletedMedtronic Vascular
Medical DeviceOct 9, 2019
Medtronic Vascular SHERPA NX ACTIVE GUIDING CATHETER, 6F HSIII, .070", REF SA6HSIII. for recall — FDA Z-2702-2019
There is a potential for extensive loss of primary segment material exposing underlying stainless-steel braid wires on a subset of 6F Sherpa catheters.
Class IFDA: CompletedMedtronic Vascular
Medical DeviceOct 9, 2019
Medtronic Vascular SHERPA NX ACTIVE GUIDING CATHETER, 6F JCL3.5, .070", REF SA6JCL35. for recall — FDA Z-2704-2019
There is a potential for extensive loss of primary segment material exposing underlying stainless-steel braid wires on a subset of 6F Sherpa catheters.
Class IFDA: CompletedMedtronic Vascular
Medical DeviceOct 9, 2019
Medtronic Vascular SHERPA NX ACTIVE GUIDING CATHETER, 6F, IMA 55CM .070", REF SA6IMAK. for recall — FDA Z-2562-2019
There is a potential for extensive loss of primary segment material exposing underlying stainless-steel braid wires on a subset of 6F Sherpa catheters.
Class IFDA: CompletedMedtronic Vascular
Medical DeviceOct 9, 2019
Medtronic Vascular SHERPA NX ACTIVE GUIDING CATHETER, 6F JL3.5, .070", REF SA6JL355. for recall — FDA Z-2750-2019
There is a potential for extensive loss of primary segment material exposing underlying stainless-steel braid wires on a subset of 6F Sherpa catheters.
Class IFDA: CompletedMedtronic Vascular
Medical DeviceOct 9, 2019
Medtronic Vascular SHERPA NX ACTIVE GUIDING CATHETER, 6F CHAMP1.5 SH, .070", REF recall — FDA Z-2737-2019
There is a potential for extensive loss of primary segment material exposing underlying stainless-steel braid wires on a subset of 6F Sherpa catheters.
Class IFDA: CompletedMedtronic Vascular
Medical DeviceOct 9, 2019
Medtronic Vascular SHERPA NX ACTIVE GUIDING CATHETER, 6F FR3.5, .070", REF SA6FR35. for recall — FDA Z-2722-2019
There is a potential for extensive loss of primary segment material exposing underlying stainless-steel braid wires on a subset of 6F Sherpa catheters.
Class IFDA: CompletedMedtronic Vascular
Medical DeviceOct 9, 2019
Medtronic Vascular SHERPA NX ACTIVE GUIDING CATHETER, 6F SCR5.0, .070", REF SA6SCR50. for recall — FDA Z-2728-2019
There is a potential for extensive loss of primary segment material exposing underlying stainless-steel braid wires on a subset of 6F Sherpa catheters.
Class IFDA: CompletedMedtronic Vascular
Medical DeviceOct 9, 2019
Medtronic Vascular SHERPA NX ACTIVE GUIDING CATHETER, 6F EBU3.5, .070", REF SA6EBU30. for recall — FDA Z-2622-2019
There is a potential for extensive loss of primary segment material exposing underlying stainless-steel braid wires on a subset of 6F Sherpa catheters.
Class IFDA: CompletedMedtronic Vascular
Medical DeviceOct 9, 2019
Medtronic Vascular SHERPA NX ACTIVE GUIDING CATHETER, 6F, SR4.0 SH, 100CM, 070", REF recall — FDA Z-2609-2019
There is a potential for extensive loss of primary segment material exposing underlying stainless-steel braid wires on a subset of 6F Sherpa catheters.
Class IFDA: CompletedMedtronic Vascular
Medical DeviceOct 9, 2019
Medtronic Vascular SHERPA NX ACTIVE GUIDING CATHETER, 6F RRAD, .070", REF SA6RRAD. for recall — FDA Z-2712-2019
There is a potential for extensive loss of primary segment material exposing underlying stainless-steel braid wires on a subset of 6F Sherpa catheters.
Class IFDA: CompletedMedtronic Vascular
Medical DeviceOct 9, 2019
Medtronic Vascular SHERPA NX ACTIVE GUIDING CATHETER, 6F AL1.5, .070", REF SA6AL15. for recall — FDA Z-2659-2019
There is a potential for extensive loss of primary segment material exposing underlying stainless-steel braid wires on a subset of 6F Sherpa catheters.
Class IFDA: CompletedMedtronic Vascular
Medical DeviceOct 9, 2019
Medtronic Vascular SHERPA NX ACTIVE GUIDING CATHETER, 6F SAR2.0 .070", REF SA6SAR20. for recall — FDA Z-2744-2019
There is a potential for extensive loss of primary segment material exposing underlying stainless-steel braid wires on a subset of 6F Sherpa catheters.
Class IFDA: CompletedMedtronic Vascular
Medical DeviceOct 9, 2019
Inter-Med Vista Dental Products 3% Sodium Hypochlorite, 10- 3cc Pre-filled Syringes, REF recall — FDA Z-0015-2020
The affected lots may be packaged in syringes which include an incorrect bung. The incorrect bung is made of a latex-free isoprene rubber material. After prolonged storage and exposure to…
Class IIFDA: TerminatedInter-Med LLC
Medical DeviceOct 9, 2019
Medtronic Vascular SHERPA NX ACTIVE GUIDING CATHETER, 6F, JL3.5, 110CM, 070", REF SA6JL35A. recall — FDA Z-2588-2019
There is a potential for extensive loss of primary segment material exposing underlying stainless-steel braid wires on a subset of 6F Sherpa catheters.
Class IFDA: CompletedMedtronic Vascular
Medical DeviceOct 9, 2019
Medtronic Vascular SHERPA NX ACTIVE GUIDING CATHETER, 6F 3DRIGHT SH .070", REF SA63DRIGHTSH. recall — FDA Z-2649-2019
There is a potential for extensive loss of primary segment material exposing underlying stainless-steel braid wires on a subset of 6F Sherpa catheters.
Class IFDA: CompletedMedtronic Vascular
Medical DeviceOct 9, 2019
Medtronic Vascular SHERPA NX ACTIVE GUIDING CATHETER, 6F EBU3.5, .070", REF SA6EBU35. for recall — FDA Z-2617-2019
There is a potential for extensive loss of primary segment material exposing underlying stainless-steel braid wires on a subset of 6F Sherpa catheters.
Class IFDA: CompletedMedtronic Vascular
Medical DeviceOct 9, 2019
Medtronic Vascular SHERPA NX ACTIVE GUIDING CATHETER, 6F MAC4.0 SH, .070", REF SA6MAC40SH. recall — FDA Z-2729-2019
There is a potential for extensive loss of primary segment material exposing underlying stainless-steel braid wires on a subset of 6F Sherpa catheters.
Class IFDA: CompletedMedtronic Vascular
How to use this monthly recall archive
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.