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Medtronic recalls SCHRITTMACHER ANGIO X3; Item Number: 4045255423347
Recalled June 21, 2017 · FDA recall Z-2548-2017 · Medtronic
Hazard
Potential for an incomplete seal on the inner package, which may result in premature degradation of the suture material. · FDA Class II
Units
478,465 (total for all products)
Sold at
Worldwide distribution. US Nationwide including PR, and countries of AU, BE, CA, CL, CN, IL, IT, JP, KR, MX, PA, SA, SG, and TR.
Description
Potential for an incomplete seal on the inner package, which may result in premature degradation of the suture material.
Product
SCHRITTMACHER ANGIO X3; Item Number: 4045255423347
Manufacturer(s)
Medtronic
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →