Medical Device
Manufacturing
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Device recalls

Recall records from FDA, newest initiation date first.

Every device recall MDM has ingested. The recall record supplies the product, the reason and the product code; the matching enforcement report supplies the Class I, II or III classification. Where the two have not been joined, the class is left blank rather than assumed.

Data as of , the FDA export date. FDA medical device recall database

59,460 records, page 1190 of 1190
FDA device recalls, page 1190 of 1190
Recall numberClassProductRecalling firmProduct codeInitiated
Z-1044-2013Class IISIEMENS brand COHERENCE RT Therapist versions RTT MR1.5, RTT 2.1/2.1A and RTT 2.2/ 2.2B...Siemens Medical Solutions USA, Inc.IYE
Z-1043-2013Class IISIEMENS brand COHERENCE RT Therapist versions RTT MR1.5, RTT 2.1/2.1A and RTT 2.2/ 2.2B...Siemens Medical Solutions USA, Inc.IYE
Z-1042-2013Class IISIEMENS brand COHERENCE RT Therapist versions RTT MR1.5, RTT 2.1/2.1A and RTT 2.2/ 2.2B...Siemens Medical Solutions USA, Inc.IYE
Z-1041-2013Class IISIEMENS brand COHERENCE RT Therapist versions RTT MR1.5, RTT 2.1/2.1A and RTT 2.2/ 2.2B...Siemens Medical Solutions USA, Inc.IYE
Z-1040-2013Class IISIEMENS brand COHERENCE RT Therapist versions RTT MR1.5, RTT 2.1/2.1A and RTT 2.2/ 2.2B...Siemens Medical Solutions USA, Inc.IYE
Z-1039-2013Class IISIEMENS brand COHERENCE RT Therapist versions RTT MR1.5, RTT 2.1/2.1A and RTT 2.2/ 2.2B...Siemens Medical Solutions USA, Inc.IYE
Z-1038-2013Class IISIEMENS brand COHERENCE RT Therapist versions RTT MR1.5, RTT 2.1/2.1A and RTT 2.2/ 2.2B...Siemens Medical Solutions USA, Inc.IYE
Z-1037-2013Class IISIEMENS brand COHERENCE RT Therapist versions RTT MR1.5, RTT 2.1/2.1A and RTT 2.2/ 2.2B...Siemens Medical Solutions USA, Inc.IYE
Z-1036-2013Class IISIEMENS brand COHERENCE RT Therapist versions RTT MR1.5, RTT 2.1/2.1A and RTT 2.2/ 2.2B...Siemens Medical Solutions USA, Inc.IYE
Z-0660-2013Class IIPT113950 PT HYBRID Glenoid Post Regenerex porous titanium construct Sterile...Zimmer GmbHKWS