Class IIOngoingZ-3220-2026
Midmark Corporation recalls Midmark IQvitals Zone
A performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used.
Midmark CorporationOHSep 30, 2026
Recalls: Process change control
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 1–12 of 117 recalls
Class IIOngoingZ-3219-2026
Midmark Corporation recalls Midmark IQvitals Zone
A performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used.
Midmark CorporationOHSep 30, 2026
Class IIOngoingZ-3218-2026
Midmark Corporation recalls Midmark IQvitals Zone
A performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used.
Midmark CorporationOHSep 30, 2026
Class IIOngoingZ-3217-2026
Midmark Corporation recalls Midmark IQvitals Zone
A performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used.
Midmark CorporationOHSep 30, 2026
Class IIOngoingZ-3206-2026
Howmedica Osteonics Corp. recalls SCORPIO C-DOME PATELLA 73-2710 73-2910 SCORPIO U-DOME PATELLA 73-3110 73-…
Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years.…
- Polymer/Metal/Polymer Cemented Semi-Constrained Partial Knee Patellofemorotibial Prosthesis
- Process change control
Howmedica Osteonics Co…NJSep 23, 2026
Class IIOngoingZ-3205-2026
Howmedica Osteonics Corp. recalls SCORPIO + MOBILE BEARING PCS 78-5-0910 SYSTEM ONE BIPOLAR 40MM 6074-4022 S…
Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years.…
Howmedica Osteonics Co…NJSep 23, 2026
Class IIOngoingZ-3204-2026
Howmedica Osteonics Corp. recalls TRIDENT 0¿ POLY INSERT 28mm ID 620-00-28D Orthopaedic implant components manuf…
Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years.…
- Calcium Phosphate Non-Porous Metal / Polymer Uncemented Semi-Constrained Hip Prosthesis
- Process change control
Howmedica Osteonics Co…NJSep 23, 2026
Class IIOngoingZ-3203-2026
Howmedica Osteonics Corp. recalls SCORPIO RECESSED METAL BACKED PATELLA 3045-0026 3045-0028 3045-0030 3045-0032…
Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years.…
- Polymer/Metal/Polymer Coated Porous Uncemented Semi-Constrained Patello/Femorotibial Knee Prosthesis
- Process change control
Howmedica Osteonics Co…NJSep 23, 2026
Class IIOngoingZ-3202-2026
Howmedica Osteonics Corp. recalls BEARING AND AXLE BUSHING ASSY STD ELBOW C-M113-1-301 KRH REV TIB INS 16mm THK .6…
Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years.…
Howmedica Osteonics Co…NJSep 23, 2026
Class IIOngoingZ-3201-2026
Howmedica Osteonics Corp. recalls ACETABULAR CUP UHMWPE 61-3258 ALL POLY CONSTRAINED INSERT 44MM 69-2244 AL…
Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years.…
Howmedica Osteonics Co…NJSep 23, 2026
Class IIOngoingZ-3200-2026
Howmedica Osteonics Corp. recalls DURACON XL ANGLED TIB INS 11/14MM C-M064-1-300 SELF-PRESSURIZING GLENOID SIZE 8…
Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years.…
Howmedica Osteonics Co…NJSep 23, 2026
Class IIOngoingZ-3199-2026
Howmedica Osteonics Corp. recalls ABG I ACETABULAR INSERT HOODED 28mm ID X 48mm C-M079-2-801 ARC2F ACETABULAR…
Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years.…
Howmedica Osteonics Co…NJSep 23, 2026