Class IIOngoingZ-1408-2025
Premier Dental Products Co recalls Premier Solo Diamond - Large Invented Cone
The hardness not meeting the material specification and may cause the diamond bur to bend.
Premier Dental Product…PAApr 2, 2025
Recalls in Pennsylvania
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 505–516 of 581 recalls
Class IIOngoingZ-1397-2025
B Braun Medical Inc recalls Introcan Safety 3 Closed IV Catheter 22 Ga. x 1 in.
Increased risk for valve housing detachment causing leakage.
B Braun Medical IncPAMar 26, 2025
Class IIOngoingZ-1312-2025
Aesculap Inc recalls Numerous models of nonsterile hemostatic forceps: (1) REF BH951R
The forceps have been used in ways not covered by the design resulting in breakage of the clamps.
Aesculap IncPAMar 19, 2025
Class IIOngoingZ-1311-2025
Aesculap Inc recalls Numerous models of nonsterile hemostatic forceps: (1) REF FB458R
The forceps have been used in ways not covered by the design resulting in breakage of the clamps.
Aesculap IncPAMar 19, 2025
Class IIOngoingZ-1310-2025
Aesculap Inc recalls Numerous models of nonsterile hemostatic forceps: (1) REF BH198R
The forceps have been used in ways not covered by the design resulting in breakage of the clamps.
Aesculap IncPAMar 19, 2025
Class IIOngoingZ-1309-2025
Aesculap Inc recalls Numerous models of nonsterile hemostatic forceps: (1) REF BH100R
The forceps have been used in ways not covered by the design resulting in breakage of the clamps.
Aesculap IncPAMar 19, 2025
Class IIOngoingZ-1308-2025
Aesculap Inc recalls Numerous models of nonsterile hemostatic forceps: (1) REF BJ500R
The forceps have been used in ways not covered by the design resulting in breakage of the clamps.
Aesculap IncPAMar 19, 2025
Class IIOngoingZ-1276-2025
Hiossen Inc. recalls Osstem Implant System - Abutment: ET Multi AbutmentSize: 4.8D 5.0GH - Abutment is inte…
Patient chart stickers provided inside the packaging may incorrectly identify ET Rigid Abutments as Regular version whereas the actual product is a Mini version;…
Hiossen Inc.PAMar 12, 2025
Class IIOngoingZ-1275-2025
Hiossen Inc. recalls ET Rigid Abutment (Mini) Size: 4.5D 2.0G/H 4.0H- Intended for use with a dental implant…
Patient chart stickers provided inside the packaging may incorrectly identify ET Rigid Abutments as Regular version whereas the actual product is a Mini version;…
Hiossen Inc.PAMar 12, 2025
Class IIOngoingZ-1274-2025
Hiossen Inc. recalls Osstem Implant System - Abutment ET Multi Abutment Size: 4.8D 3.0G/H- Abutment is inte…
Patient chart stickers provided inside the packaging may incorrectly identify ET Rigid Abutments as Regular version whereas the actual product is a Mini version;…
Hiossen Inc.PAMar 12, 2025
Class IIOngoingZ-1273-2025
Hiossen Inc. recalls ET Rigid Abutment (Mini) SIze: 4.5D 4.0G/H 4.0H - Intended for use with a dental implan…
Patient chart stickers provided inside the packaging may incorrectly identify ET Rigid Abutments as Regular version whereas the actual product is a Mini version;…
Hiossen Inc.PAMar 12, 2025
Class IIOngoingZ-1272-2025
Hiossen Inc. recalls ET Rigid Abutment (Mini) SIze: 4.5D 3.0G/H 7.0H - Intended for use with a dental implan…
Patient chart stickers provided inside the packaging may incorrectly identify ET Rigid Abutments as Regular version whereas the actual product is a Mini version;…
Hiossen Inc.PAMar 12, 2025