Medical Device Recalls
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11 to 13 of 13 Results
Related Medical Device Recalls |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Z-1245-2018 - 1. Femoral Canal Pressurizer without Hub, Medium, Blue, Product Number: 0206-546-000, UDI: (01)4546540039552; 2. Femoral Canal Pressurizer without Hub, Large, Red, Product Number: 0206-547-000, UDI: (... | 2 | 03/28/2018 | Stryker Instruments Div. of Stryker Corporation |
Z-1250-2018 - 1. AutoPlex System, Product Number: 0605-887-000, UDI: (01)4546540593108; 2. AutoPlex System: w/ VertaPlex HV, Product Number: 0607-687-000, UDI: (01)7613252039259 Bone cement. | 2 | 03/28/2018 | Stryker Instruments Div. of Stryker Corporation |
Z-1254-2018 - 1. 11g/10mm iVAS System Kit, Product Number: 0705-310-000, UDI: (01)7613252505983; 2. 11g/15mm iVAS System Kit, Product Number: 0705-315-000, UDI: (01)7613252505969 for spinal orthopedic use. ... | 2 | 03/28/2018 | Stryker Instruments Div. of Stryker Corporation |
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