Medical devices, 2020
Shortlist up to four to read them side by side.
3,055 medical device recalls FDA’s Enforcement Report published in 2020, newest first; 40,450 in all since 2012.
FDA’s medical device recalls, as its Enforcement Report classifies them, from June 2012. Lists of FDA’s records can’t be saved for alerts: openFDA asks that its data not be used to alert the public (openFDA); FDA’s own emails do that. Copied Nov 5, 2026.
3,055of 3,055 medical device recallsshown with your filters
The list
- Medical device recall ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 22 mm, Neutral, O.D Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Class IIFDA’s classNov 11, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 11, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 26 mm, Neutral, O.D Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Class IIFDA’s classNov 11, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 11, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 28 mm, Neutral, O.D Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Class IIFDA’s classNov 11, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 11, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 32 mm, Neutral, O.D Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Class IIFDA’s classNov 11, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 11, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 22 mm, Neutral, O.D Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Class IIFDA’s classNov 11, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 11, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 26 mm, Neutral, O.D Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Class IIFDA’s classNov 11, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 11, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 28 mm, Neutral, O.D Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Class IIFDA’s classNov 11, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 11, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 32 mm, Neutral, O.D Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Class IIFDA’s classNov 11, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 11, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 22 mm, Neutral, O.D Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Class IIFDA’s classNov 11, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 11, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 26 mm, Neutral, O.D Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Class IIFDA’s classNov 11, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 11, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 28 mm, Neutral, O.D Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Class IIFDA’s classNov 11, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 11, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 32 mm, Neutral, O.D Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Class IIFDA’s classNov 11, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 11, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 22 mm, 10 degree inclined face, O.D Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Class IIFDA’s classNov 11, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 11, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 22 mm, 10 degree inclined face, O.D Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Class IIFDA’s classNov 11, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 11, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 26 mm, 10 degree inclined face, O.D Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Class IIFDA’s classNov 11, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 11, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 22 mm, 10 degree inclined face, O.D Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Class IIFDA’s classNov 11, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 11, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 26 mm, 10 degree inclined face, O.D Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Class IIFDA’s classNov 11, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 11, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 28 mm, 10 degree inclined face, O.D Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Class IIFDA’s classNov 11, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 11, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 22 mm, 10 degree inclined face, O.D Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Class IIFDA’s classNov 11, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 11, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 26 mm, 10 degree inclined face, O.D Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Class IIFDA’s classNov 11, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 11, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 28 mm, 10 degree inclined face, O.D Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Class IIFDA’s classNov 11, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 11, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 32 mm, 10 degree inclined face, O.D Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Class IIFDA’s classNov 11, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 11, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 22 mm, 10 degree inclined face, O.D Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Class IIFDA’s classNov 11, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 11, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 26 mm, 10 degree inclined face, O.D Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Class IIFDA’s classNov 11, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 11, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 28 mm, 10 degree inclined face, O.D Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Class IIFDA’s classNov 11, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 11, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 32 mm, 10 degree inclined face, O.D Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Class IIFDA’s classNov 11, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 11, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 22 mm, 10 degree inclined face, O.D Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Class IIFDA’s classNov 11, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 11, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 26 mm, 10 degree inclined face, O.D Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Class IIFDA’s classNov 11, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 11, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 28 mm, 10 degree inclined face, O.D Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Class IIFDA’s classNov 11, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 11, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 32 mm, 10 degree inclined face, O.D Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Class IIFDA’s classNov 11, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 11, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 22 mm, 10 degree inclined face, O.D Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Class IIFDA’s classNov 11, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 11, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 26 mm, 10 degree inclined face, O.D Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Class IIFDA’s classNov 11, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 11, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 28 mm, 10 degree inclined face, O.D Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Class IIFDA’s classNov 11, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 11, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 32 mm, 10 degree inclined face, O.D Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Class IIFDA’s classNov 11, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 11, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 22 mm, 10 degree inclined face, O.D Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Class IIFDA’s classNov 11, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 11, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 26 mm, 10 degree inclined face, O.D Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Class IIFDA’s classNov 11, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 11, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 28 mm, 10 degree inclined face, O.D Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Class IIFDA’s classNov 11, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 11, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 32 mm, 10 degree inclined face, O.D Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Class IIFDA’s classNov 11, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 11, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 22 mm, 10 degree inclined face, O.D Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Class IIFDA’s classNov 11, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 11, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 26 mm, 10 degree inclined face, O.D Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Class IIFDA’s classNov 11, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 11, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 28 mm, 10 degree inclined face, O.D Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Class IIFDA’s classNov 11, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 11, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 32 mm, 10 degree inclined face, O.D Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Class IIFDA’s classNov 11, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 11, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 22 mm, 10 degree inclined face, O.D Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Class IIFDA’s classNov 11, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 11, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 26 mm, 10 degree inclined face, O.D Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Class IIFDA’s classNov 11, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 11, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 28 mm, 10 degree inclined face, O.D Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Class IIFDA’s classNov 11, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 11, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 32 mm, 10 degree inclined face, O.D Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Class IIFDA’s classNov 11, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 11, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 32 mm, Snap-In O.D Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Class IIFDA’s classNov 11, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 11, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 32 mm, Snap-In O.D Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Class IIFDA’s classNov 11, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 11, 2020ClassClass IIStatusTerminatedWhereNationwide
Nothing matches all of these.
Remove a filter to see more. Each one is a fact FDA’s record publishes, so a recall can be left out because its record is silent on it.
Source:
FDA, Device recall enforcement reports. Released Nov 3, 2026. Updated weekly.
Recalls of food, medicines, medical devices, pet food and animal drugs are from the U.S. Food and Drug Administration (FDA). FDA does not endorse Hearth Record. openFDA: “Do not rely on openFDA to make decisions regarding medical care.”
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