Medical DeviceJun 21, 2017
Medtronic SCHRITTMACHER ANGIO X3 recall — FDA Z-2548-2017
Potential for an incomplete seal on the inner package, which may result in premature degradation of the suture material.
Class IIFDA: TerminatedMedtronic
Recall history in this database
Classification mix: Class II: 8.
Medical DeviceJun 21, 2017
Medtronic CUSTOM SUTURE PACK recall — FDA Z-2547-2017
Potential for an incomplete seal on the inner package, which may result in premature degradation of the suture material.
Class IIFDA: TerminatedMedtronic
Medical DeviceJun 21, 2017
Medtronic Sutures. BIOSYN: BIOSYN 4/0 18" VIOLET CV-25 DT, Item Number: GMJ34M recall — FDA Z-2544-2017
Potential for an incomplete seal on the inner package, which may result in premature degradation of the suture material.
Class IIFDA: TerminatedMedtronic
Medical DeviceJun 21, 2017
Medtronic Sutures. ENDO STITCH: ENDO STITCH POLYSORB 0 48" U/D DLU SU, Item Number: 170056 recall — FDA Z-2543-2017
Potential for an incomplete seal on the inner package, which may result in premature degradation of the suture material.
Class IIFDA: TerminatedMedtronic
Medical DeviceJun 21, 2017
Medtronic Best Practice Kit, Item Numbers: 00Z2064, 00Z2150, 00Z2190, 00Z2192, 00Z2211 recall — FDA Z-2545-2017
Potential for an incomplete seal on the inner package, which may result in premature degradation of the suture material.
Class IIFDA: TerminatedMedtronic
Medical DeviceJun 21, 2017
Medtronic USPACK-SUTURE KIT; Item Number: US1672 recall — FDA Z-2546-2017
Potential for an incomplete seal on the inner package, which may result in premature degradation of the suture material.
Class IIFDA: TerminatedMedtronic
Medical DeviceJun 21, 2017
Medtronic Sutures. MAXON: MAXON 4/0 5X18" GREEN CV-24 D-TACH; Item Number: 8886621933; MAXON recall — FDA Z-2542-2017
Potential for an incomplete seal on the inner package, which may result in premature degradation of the suture material.
Class IIFDA: TerminatedMedtronic
Medical DeviceJun 21, 2017
Medtronic Sutures. POLYSORB: POLSORB 0 18 U/D PRECUT 126R, Item Number: L4; POLSORB 0 18 VIO recall — FDA Z-2541-2017
Potential for an incomplete seal on the inner package, which may result in premature degradation of the suture material.
Class IIFDA: TerminatedMedtronic
Understanding this recall history
This page summarizes recall records in which the official source identifies Medtronic as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.