Medical devices, 2021
Shortlist up to four to read them side by side.
2,303 medical device recalls FDA’s Enforcement Report published in 2021, 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 6, 2026.
2,303of 2,303 medical device recallsshown with your filters
The list
- Medical device recall INJECTOR FORCEMAX LOWER 23G 4MM Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Class IIFDA’s classFeb 17, 2021in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 17, 2021ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall INJECTOR FORCEMAX LOWER 25G 2.5MM Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Class IIFDA’s classFeb 17, 2021in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 17, 2021ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall INJECTOR FORCEMAX LOWER 23G 5MM Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Class IIFDA’s classFeb 17, 2021in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 17, 2021ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall INJECTOR FORCEMAX LOWER 25G 5MM Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Class IIFDA’s classFeb 17, 2021in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 17, 2021ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall INJECTOR FORCEMAX LOWER 23G 6MM Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Class IIFDA’s classFeb 17, 2021in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 17, 2021ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall INJECTOR FORCEMAX LOWER 25G 6MM Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Class IIFDA’s classFeb 17, 2021in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 17, 2021ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall INJECTOR FORCEMAX SIF 270CM 23G 4MM Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Class IIFDA’s classFeb 17, 2021in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 17, 2021ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall INJECTOR FORCEMAX UP 2.8MMCH 21G 4MM Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Class IIFDA’s classFeb 17, 2021in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 17, 2021ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall INJECTOR FORCEMAX UP 2.8MMCH 21G 6MM Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Class IIFDA’s classFeb 17, 2021in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 17, 2021ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall INJECTOR FORCEMAX UP 2.8MMCH 23G 5MM Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Class IIFDA’s classFeb 17, 2021in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 17, 2021ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall INJECTOR FORCEMAX UP 2.8MMCH 23G 6MM Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Class IIFDA’s classFeb 17, 2021in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 17, 2021ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall INJECTOR FORCEMAX UP 2.8MMCH 25G 4MM Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Class IIFDA’s classFeb 17, 2021in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 17, 2021ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall INJECTOR FORCEMAX UP 2.8MMCH 25G 5MM Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Class IIFDA’s classFeb 17, 2021in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 17, 2021ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall INJECTOR FORCEMAX UP 2.8MMCH 25G 6MM Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Class IIFDA’s classFeb 17, 2021in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 17, 2021ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall INJECTOR FORCEMAX LOWER 23G 3MM Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Class IIFDA’s classFeb 17, 2021in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 17, 2021ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall INJECTOR FORCEMAX LOWER 23G 4MM Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Class IIFDA’s classFeb 17, 2021in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 17, 2021ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall INJECTOR FORCEMAX 25G 2.5MM Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Class IIFDA’s classFeb 17, 2021in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 17, 2021ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall INJECTOR FORCEMAX LOWER 23G 5MM Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Class IIFDA’s classFeb 17, 2021in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 17, 2021ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall INJECTOR FORCEMAX LOWER 23G 6MM 5/BX Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Class IIFDA’s classFeb 17, 2021in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 17, 2021ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall INJECTOR FORCEMAX LOWER 25G 5MM Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Class IIFDA’s classFeb 17, 2021in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 17, 2021ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall INJECTOR FORCEMAX LOWER 25G 6MM Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Class IIFDA’s classFeb 17, 2021in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 17, 2021ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall INJECTOR FORCEMAX SIF 270CM 23G 4MM Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Class IIFDA’s classFeb 17, 2021in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 17, 2021ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall INJECTOR FORCEMAX SIF 270CM 23G 4MM Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Class IIFDA’s classFeb 17, 2021in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 17, 2021ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall INJECTOR FORCEMAX UP 2MM CH 25G 4MM Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Class IIFDA’s classFeb 17, 2021in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 17, 2021ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall INJECTOR FORCEMAX UP 2MM CH 23G 3MM Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Class IIFDA’s classFeb 17, 2021in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 17, 2021ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall INJECTOR FORCEMAX UP 2MM CH 25G 5MM Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Class IIFDA’s classFeb 17, 2021in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 17, 2021ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall INJECTOR FORCEMAX UP 2MM CH 23G 6MM Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Class IIFDA’s classFeb 17, 2021in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 17, 2021ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall INJECTOR FORCEMAX UP 2MM CH 25G 6MM Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Class IIFDA’s classFeb 17, 2021in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 17, 2021ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall NEEDLEMASTER 4MMx 21G UPPER Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Class IIFDA’s classFeb 17, 2021in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 17, 2021ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall NEEDLEMASTER 4MMx 23G UPPER Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Class IIFDA’s classFeb 17, 2021in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 17, 2021ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall NEEDLEMASTER 4MMx 25G UPPER Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Class IIFDA’s classFeb 17, 2021in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 17, 2021ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall NEEDLEMASTER 4MMx 26G UPPER Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Class IIFDA’s classFeb 17, 2021in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 17, 2021ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall NEEDLEMASTER 5MMx 21G UPPER Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Class IIFDA’s classFeb 17, 2021in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 17, 2021ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall NEEDLEMASTER 3MMx 23G LOWER Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Class IIFDA’s classFeb 17, 2021in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 17, 2021ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall NEEDLEMASTER 5MMx 25G UPPER Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Class IIFDA’s classFeb 17, 2021in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 17, 2021ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall NEEDLEMASTER 6MMx 21G UPPER Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Class IIFDA’s classFeb 17, 2021in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 17, 2021ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall NEEDLEMASTER 6MMx 23G UPPER Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Class IIFDA’s classFeb 17, 2021in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 17, 2021ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall NEEDLEMASTER 6MMx 25G UPPER Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Class IIFDA’s classFeb 17, 2021in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 17, 2021ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall NEEDLEMASTER 3MMx 23G LOWER Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Class IIFDA’s classFeb 17, 2021in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 17, 2021ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall NEEDLEMASTER 3MMx 26G LOWER Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Class IIFDA’s classFeb 17, 2021in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 17, 2021ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall NEEDLEMASTER 4MMx 23G LOWER Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Class IIFDA’s classFeb 17, 2021in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 17, 2021ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall NEEDLEMASTER 4MMx 25G LOWER Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Class IIFDA’s classFeb 17, 2021in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 17, 2021ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall NEEDLEMASTER 4MMx 26G LOWER Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Class IIFDA’s classFeb 17, 2021in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 17, 2021ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall NEEDLEMASTER 3MMx 23G LOWER Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Class IIFDA’s classFeb 17, 2021in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 17, 2021ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall NEEDLEMASTER 5MMx 25G LOWER Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Class IIFDA’s classFeb 17, 2021in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 17, 2021ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall NEEDLEMASTER 6MMx 23G LOWER Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Class IIFDA’s classFeb 17, 2021in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 17, 2021ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall NEEDLEMASTER 6MMx 25G LOWER Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Class IIFDA’s classFeb 17, 2021in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 17, 2021ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall NEEDLEMASTER 1.8MMx 26G LOWER Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Class IIFDA’s classFeb 17, 2021in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 17, 2021ClassClass 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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