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  1. FDA Recalls
  2. ›Device Recalls

FDA Device Recalls

Recalls of medical devices, diagnostic equipment, implants, and surgical instruments.

Classification
AllClass IClass IIClass III
Status
AllOngoingCompletedTerminated
Date
All timePast 30 daysPast 12 months

Showing 561–580 of 1,000 recalls

Class IIOngoing

GEM Premier 5000 PAK; Part No. 00055360010.

Instrumentation Laboratory

Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution Not Detected (PCSND) errors during warm-up, including consecutive occurrences, resulting in GEM PAK ejection and requiring insertion of a new GEM PAK. iQM2 is an active quality process control program designed to provide continuous monitoring of the entire testing process. Thus, if a GEM PAK completes AutoPAK Validation following warm-up, it may remain in use. Consecutive GEM PAK ejections during warm-up may prolong turnaround times, potentially delaying results. In such cases, patient management may require reassessment once results are available. While many GEM PAKs continue to perform as intended, consecutive ejections may increase the likelihood of operational disruption, highlighting the importance of advance planning where feasible to help minimize impact.

January 20, 2026 · DeviceView details →
Class IIOngoing

GEM Premier 5000 PAK; Part No. 00055415004.

Instrumentation Laboratory

Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution Not Detected (PCSND) errors during warm-up, including consecutive occurrences, resulting in GEM PAK ejection and requiring insertion of a new GEM PAK. iQM2 is an active quality process control program designed to provide continuous monitoring of the entire testing process. Thus, if a GEM PAK completes AutoPAK Validation following warm-up, it may remain in use. Consecutive GEM PAK ejections during warm-up may prolong turnaround times, potentially delaying results. In such cases, patient management may require reassessment once results are available. While many GEM PAKs continue to perform as intended, consecutive ejections may increase the likelihood of operational disruption, highlighting the importance of advance planning where feasible to help minimize impact.

January 20, 2026 · DeviceView details →
Class IIOngoing

GEM Premier 5000; Part No. 00055445010 & 00055445011.

Instrumentation Laboratory

Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution Not Detected (PCSND) errors during warm-up, including consecutive occurrences, resulting in GEM PAK ejection and requiring insertion of a new GEM PAK. iQM2 is an active quality process control program designed to provide continuous monitoring of the entire testing process. Thus, if a GEM PAK completes AutoPAK Validation following warm-up, it may remain in use. Consecutive GEM PAK ejections during warm-up may prolong turnaround times, potentially delaying results. In such cases, patient management may require reassessment once results are available. While many GEM PAKs continue to perform as intended, consecutive ejections may increase the likelihood of operational disruption, highlighting the importance of advance planning where feasible to help minimize impact.

January 20, 2026 · DeviceView details →
Class IIOngoing

GEM Premier 5000 PAK; Part No. 00055407504.

Instrumentation Laboratory

Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution Not Detected (PCSND) errors during warm-up, including consecutive occurrences, resulting in GEM PAK ejection and requiring insertion of a new GEM PAK. iQM2 is an active quality process control program designed to provide continuous monitoring of the entire testing process. Thus, if a GEM PAK completes AutoPAK Validation following warm-up, it may remain in use. Consecutive GEM PAK ejections during warm-up may prolong turnaround times, potentially delaying results. In such cases, patient management may require reassessment once results are available. While many GEM PAKs continue to perform as intended, consecutive ejections may increase the likelihood of operational disruption, highlighting the importance of advance planning where feasible to help minimize impact.

January 20, 2026 · DeviceView details →
Class IIOngoing

MediHoney Gel with Active Leptospermum Honey. Model/Catalog Numbers: (1) 31805, (2) 31815. MediHoney Gel dressing with Active Leptospermum Honey provides a moist environment conducive to wound healing and is indicated for light to moderately exuding wounds.

Integra LifeSciences Corp. (NeuroSciences)

Potential packaging failures, which could lead to a breach in the sterile barrier.

January 16, 2026 · DeviceView details →
Class IIOngoing

Private Label CVS. Model Number: CVS405406. Helps maintain a moist wound environment, which has shown to be conducive to wound healing. Intended for minor scalds & burns, minor cuts, lacerations & minor abrasions.

Integra LifeSciences Corp. (NeuroSciences)

Potential packaging failures, which could lead to a breach in the sterile barrier.

January 16, 2026 · DeviceView details →
Class IIOngoing

GE Healthcare Centricity Universal Viewer Zero Footprint Client, Model Numbers: 2110344-039, 2110344-046, 2110344-047; System, Image Processing, Radiological

GE Healthcare

Under certain workflows, patient information shown in the viewer may not match the images displayed on Centricity Universal Viewer Zero Footprint Client (ZFP) with versions ZFP v6.0: SP11.6, SP11.6.0.1 and SP11.6.1 on systems with Patient Timeline installed,

January 16, 2026 · DeviceView details →
Class IIOngoing

MEDIHONEY CALCIUM ALGINATE WITH ACTIVE LEPTOSPERMUM HONEY. Model Numbers: (1) 31012, (2) 31022, (3) 31045. MEDIHONEY CALCIUM ALGINATE DRESSING WITH ACTIVE LEPTOSPERMUM HONEY supports and aids autolytic debridement and is indicated for the management of moderately to heavily exuding wounds

Integra LifeSciences Corp. (NeuroSciences)

Potential packaging failures, which could lead to a breach in the sterile barrier.

January 16, 2026 · DeviceView details →
Class IIOngoing

Brand Name: Reverse Shoulder Prosthesis (RSP) Product Name: RSP HUMERAL SOCKET INSERT, 32MM +4MM, STANDARD HXe-plus Model/Catalog Number: 509-00-432

Encore Medical, LP

Knee and Humeral socket implants contain incorrect labeling.

January 15, 2026 · DeviceView details →
Class IIOngoing

Brand Name: Reverse Shoulder Prosthesis (RSP) Product Name: RSP STANDARD HUMERAL SOCKET INSERT, 36MM, HXe-plus Model/Catalog Number: 509-00-036

Encore Medical, LP

Knee and Humeral socket implants contain incorrect labeling.

January 15, 2026 · DeviceView details →
Class IIOngoing

Brand Name: AESCULAP Product Name: MINOP TROCAR 150MM 4 WKING CHANNEL6.0MM Model/Catalog Number: FF399R Software Version: N/A Product Description: MINOP TROCAR 150MM 4 WKING CHANNEL6.0MM Component: N/A

Aesculap Inc

There is the potential for the length of the trocar shaft to be too long.

January 15, 2026 · DeviceView details →
Class IIOngoing

MEDLINE UNNA-Z STRETCH ZINC PASTE BANDAGE, REF NONUNNAS40 KOB article #40307010

KOB GmbH

Due to labeling error. Incomplete ingredients listed. Labeling did not include castor oil or calamine.

January 15, 2026 · DeviceView details →
Class IIOngoing

Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS, 7L 16MM, VE Model/Catalog Number: 341-16-707

Encore Medical, LP

Knee and Humeral socket implants contain incorrect labeling.

January 15, 2026 · DeviceView details →
Class IIOngoing

PIE PAK Models: P2HC-A, P2HC-S, P2HC

Edermy LLC

Lack of 510K clearance

January 14, 2026 · DeviceView details →
Class IIOngoing

PIE Trolley System Model: 2005

Edermy LLC

Lack of 510K clearance

January 14, 2026 · DeviceView details →
Class IIOngoing

Octopus Nuvo Tissue Stabilizer, disposable tissue stabilization system, Product Number TSMICS1

Medtronic Perfusion Systems

During the manufacturing, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to the bottom of the canister, and the long tube was attached to the top, contrary to the intended design.

January 13, 2026 · DeviceView details →
Class IIOngoing

Laerdal Compact Suction Unit 4 RTCA version (LCSU 4 RTCA) 1) LCSU 4, 800 ml, RTCA; Catalog Number: 880052; 2) LCSU 4, 300 ml, RTCA; Catalog Number: 880062; 3) LCSU 4, RTCA; Catalog Number: 881152;

Laerdal Medical Corporation

units manufactured in a limited time period may emit electromagnetic noise beyond the acceptable limits for RTCA application specified in RTCA DO-160G Chapter 21, Equipment Category M.

January 13, 2026 · DeviceView details →
Class IIOngoing

Brand Name: Spectrum IQ Product Name: Infusion Pump Model/Catalog Number: 3570009 Software Version: N/A Product Description: Infusion Pump, one unit per carton Component: N/A

Baxter Healthcare Corporation

Pumps were released without full testing being performed, including occlusion alarm testing.

January 13, 2026 · DeviceView details →
Class IIOngoing

Endo-Model Replacement Plateau; Item Number: 15-0027/11;

Waldemar Link GmbH & Co. KG (Mfg Site)

The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.

January 12, 2026 · DeviceView details →
Class IIOngoing

Endo-Model Replacement Plateau; Item Number: 15-8030/12;

Waldemar Link GmbH & Co. KG (Mfg Site)

The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.

January 12, 2026 · DeviceView details →
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