Prosthesis, Shoulder, Semi-constrained, Metal/polymer Cemented
Zimmer, Inc.'s record for this product code
Recent MDR events
146 adverse event reports on file
- ALLIANCE®Jan 30, 2024Malfunction18606114
- ZIMMER CPT STEM AND COCR HEADFeb 14, 2020InjuryMW5093027
- ZIMMER REVERSE SHOULDER REPLACEMENTSep 5, 2019InjuryMW5089608
- REVERSE CUP SHOULDERSep 18, 2018InjuryMW5079902
- REVERSE SHOULDER SYSTEMAug 15, 2017InjuryMW5071612
- UNKNOWN ZIMMER ADAPTERAug 10, 2017Injury0001822565-2017-05597
- UNKNOWN ZIMMER GLENOIDAug 10, 2017Injury0001822565-2017-05596
- UNKNOWN ZIMMER POSTAug 10, 2017Injury0001822565-2017-05600
- ZIMMER TRABECULAR METAL REVERSE VIVACIT-E HIGHLY CROSSLINKED POLYETHYLENE LINERAug 7, 2017Injury0001822565-2017-05380
- OFFSET MODULAR HUMERAL HEAD 21 MM HEAD HEIGHT 46 MM SPHERICAL HEAD DIAMETERAug 7, 2017Injury0001822565-2017-05478
Recalls
19 recall events for this product code
- TerminatedNov 6, 2012
Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Winterthur, Switzerland, after receiving four complaints of a discrepancy between product patient labels and product labels with respect to the reference and lot numbers of the product. While the information printed on the product label is correct, the info
View FDA record ↗ - TerminatedNov 6, 2012
Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Wintetthur, Switzerland, after receiving four complaints of a discrepancy between product patient labels and product labels with respect to the reference and lot numbers of the product. While the information printed on the product label is correct, the info
View FDA record ↗ - TerminatedNov 6, 2012
Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Winterthur, Switzerland, after receiving four complaints of a discrepancy between product patient labels and product labels with respect to the reference and lot numbers of the product. While the information printed on the product label is correct, the info
View FDA record ↗ - TerminatedNov 6, 2012
Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Winterthur, Switzerland, after receiving four complaints of a discrepancy between product patient labels and product labels with respect to the reference and lot numbers of the product. While the information printed on the product label is correct, the info
View FDA record ↗ - TerminatedNov 6, 2012
Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Winterthur, Switzerland, after receiving four complaints of a discrepancy between product patient labels and product labels with respect to the reference and lot numbers of the product. While the information printed on the product label is correct, the info
View FDA record ↗ - TerminatedNov 6, 2012
Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Winterthur, Switzerland, after receiving four complaints of a discrepancy between product patient labels and product labels with respect to the reference and lot numbers of the product. While the information printed on the product label is correct, the info
View FDA record ↗ - TerminatedNov 6, 2012
Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Wintetthur, Switzerland, after receiving four complaints of a discrepancy between product patient labels and product labels with respect to the reference and lot numbers of the product. While the information printed on the product label is correct, the info
View FDA record ↗ - TerminatedNov 6, 2012
Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Winterthur, Switzerland, after receiving four complaints of a discrepancy between product patient labels and product labels with respect to the reference and lot numbers of the product. While the information printed on the product label is correct, the info
View FDA record ↗ - TerminatedNov 6, 2012
Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Winterthur, Switzerland, after receiving four complaints of a discrepancy between product patient labels and product labels with respect to the reference and lot numbers of the product. While the information printed on the product label is correct, the info
View FDA record ↗ - TerminatedNov 6, 2012
Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Wintetthur, Switzerland, after receiving four complaints of a discrepancy between product patient labels and product labels with respect to the reference and lot numbers of the product. While the information printed on the product label is correct, the info
View FDA record ↗
510(k) clearances
3 clearances for this product code