Medical device recalls
39229 federal recalls on file. Federal recalls for medical devices — surgical equipment, monitors, diagnostic tools, implants, home health devices. Sourced from the FDA.
- 2017-04-05FDA-DeviceResource Optimization & Innovation LlcClass IIRegard, Item Number: 800408002, Sterile, LD0477B - C-Section PK - Spohn
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
- 2017-04-05FDA-DeviceResource Optimization & Innovation LlcClass IIRegard, Item Number: 800407004, Sterile, OR0476D - Ortho PK - Spohn
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
- 2017-04-05FDA-DeviceResource Optimization & Innovation LlcClass IIRegard, Item Number: 800401002, Sterile, GS0470B - Lap PK - Spohn
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
- 2017-04-05FDA-DeviceResource Optimization & Innovation LlcClass IIRegard, Item Number: 800401001, Sterile, GS0470A - Lap PK - Spohn
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
- 2017-04-05FDA-DeviceResource Optimization & Innovation LlcClass IIRegard, Item Number: 800623001, Sterile, NU0787A - Neuro - Medical Center Santa Rosa
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
- 2017-04-05FDA-DeviceResource Optimization & Innovation LlcClass IIRegard, Item Number: 800599001, Sterile, GS0694A - Robotic Lap - Christus Highland
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
- 2017-04-05FDA-DeviceResource Optimization & Innovation LlcClass IIRegard, Item Number: 800599001, Sterile, GS0694A - Robotic Lap - Christus Highland
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
- 2017-04-05FDA-DeviceResource Optimization & Innovation LlcClass IIRegard, Item Number: 800569003, Sterile, CV0659C - Open Heart A&B - Medical Center Santa Rosa
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
- 2017-04-05FDA-DeviceResource Optimization & Innovation LlcClass IIRegard, Item Number: 800569002, Sterile, CV0659B - Open Heart A&B - Medical Center Santa Rosa
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
- 2017-04-05FDA-DeviceResource Optimization & Innovation LlcClass IIRegard, Item Number: 800568005, Sterile, OR0658E - Titanium Rib - Childrens Santa Rosa
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
- 2017-04-05FDA-DeviceResource Optimization & Innovation LlcClass IIRegard, Item Number: 800567003, Sterile, GY0656C - Robotic Hysterectomy - Alamo
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
- 2017-04-05FDA-DeviceResource Optimization & Innovation LlcClass IIRegard, Item Number: 800567002, Sterile, GY0656B- Robotic Hysterectomy - Alamo
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
- 2017-04-05FDA-DeviceResource Optimization & Innovation LlcClass IIRegard, Item Number: 800562002, Sterile, NU0651B - Neuro - Childrens Santa Rosa
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
- 2017-04-05FDA-DeviceResource Optimization & Innovation LlcClass IIRegard, Item Number: 800560002, Sterile, GS0649B - Lap Chole - Childrens Santa Rosa
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
- 2017-04-05FDA-DeviceResource Optimization & Innovation LlcClass IIRegard, Item Number: 800559003, Sterile, ET0648C - Head & Neck - Childrens Santa Rosa
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
- 2017-04-05FDA-DeviceResource Optimization & Innovation LlcClass IIRegard, Item Number: 800559002, Sterile, ET0648B - Head & Neck - Childrens Santa Rosa
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
- 2017-04-05FDA-DeviceResource Optimization & Innovation LlcClass IIRegard, Item Number: 800559001, Sterile, ET0648A - Head & Neck - Childrens Santa Rosa
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
- 2017-04-05FDA-DeviceResource Optimization & Innovation LlcClass IIRegard, Item Number: 800558004, Sterile, OR0647D - Extremity - Childrens Santa Rosa
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
- 2017-04-05FDA-DeviceResource Optimization & Innovation LlcClass IIRegard, Item Number: 800558003, Sterile, OR0647C - Extremity - Childrens Santa Rosa
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
- 2017-04-05FDA-DeviceResource Optimization & Innovation LlcClass IIRegard, Item Number: 800558002, Sterile, OR0647B - Extremity - Childrens Santa Rosa
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
- 2017-04-05FDA-DeviceResource Optimization & Innovation LlcClass IIRegard, Item Number: 800558001, Sterile, OR0647A - Extremity - Childrens Santa Rosa
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
- 2017-04-05FDA-DeviceResource Optimization & Innovation LlcClass IIRegard, Item Number: 800557002, Sterile, LD0646B - C Section - Childrens Santa Rosa
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
- 2017-04-05FDA-DeviceResource Optimization & Innovation LlcClass IIRegard, Item Number: 800557001, Sterile, LD0646A - C Section - Childrens Santa Rosa
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
- 2017-04-05FDA-DeviceResource Optimization & Innovation LlcClass IIRegard, Item Number: 800555002, Sterile, HT0644B - Pediatric Card Cath - Childrens Santa Rosa
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
- 2017-04-05FDA-DeviceResource Optimization & Innovation LlcClass IIRegard, Item Number: 800555001, Sterile, HT0644A - Pediatric Card Cath - Childrens Santa Rosa
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
- 2017-04-05FDA-DeviceResource Optimization & Innovation LlcClass IIRegard, Item Number: 800554003, Sterile, GS0643C - Pediatric Basic - Childrens Santa Rosa
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
- 2017-04-05FDA-DeviceResource Optimization & Innovation LlcClass IIRegard, Item Number: 800553003, Sterile, OR0642C - Total Knee - Medical Center Santa Rosa
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
- 2017-04-05FDA-DeviceResource Optimization & Innovation LlcClass IIRegard, Item Number: 800553002, Sterile, OR0642B - Total Knee - Medical Center Santa Rosa
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
- 2017-04-05FDA-DeviceResource Optimization & Innovation LlcClass IIRegard, Item Number: 800553001, Sterile, OR0642A - Total Knee - Medical Center Santa Rosa
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
- 2017-04-05FDA-DeviceResource Optimization & Innovation LlcClass IIRegard, Item Number: 800551003, Sterile, GS0640C - Lap Chole - Medical Center Santa Rosa
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
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