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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 2181–2200 of 39,430 recalls

Class IIOngoing

SAFE-T-FILL Micro Capillary Blood Collection, 200 ¿L; Prepared with Clot Activator and Serum Separator Gel; Red Model/Catalog Number: 07 7120 Product Description: The SAFE-T-FILL Capillary Blood Collection System is a collection device used to draw capillary blood from the finger or heelstick.

ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.

September 26, 2025 · DeviceView details →
Class IIOngoing

SAFE-T-FILL Micro Capillary Blood Collection, 125 ¿L; Prepared with Lithium Heparin; Green Model/Catalog Number: 07 6101 Product Description: The SAFE-T-FILL Capillary Blood Collection System is a collection device used to draw capillary blood from the finger or heelstick.

ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.

September 26, 2025 · Device
View details →
Class IIOngoing

SAFE-T-FILL MicroHematocrit Capillary Tubes, 50 ¿L; Untreated, Blue Markings Model/Catalog Number: 06 0508 Product Description: A clear, plastic capillary blood collection tube

ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.

September 26, 2025 · DeviceView details →
Class IIOngoing

SAFE-T-FILL Micro Capillary Blood Collection, 200 ¿L; Prepared with Clot Activator; Red Model/Catalog Number: 07 7150 Product Description: The SAFE-T-FILL Capillary Blood Collection System is a collection device used to draw capillary blood from the finger or heelstick.

ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.

September 26, 2025 · DeviceView details →
Class IIOngoing

B105P, B125P, B105M, B125M, B155M Patient Monitors; Model nos. 6160000-002 6160000-003 6160000-004 6160000-005 6160000-101 6160000-102 6160000-103 6160000-104 6160000-105 6160001-063 6160001-064 6160001-065 Monitor, Physiological, Patient (With Arrhythmia Detection or Alarms 3/19/26 updated to add B105P Patient Monitor 6160001-061 B125P Patient Monitor 6160001-062 B105M-C Patient Monitor 6160002-033 B105M-A Patient Monitor 6160000-113 B155M-A Patient Monitor 6160000-115 B125P-B Patient Monitor 6160002-022 B105M-B Patient Monitor 6160002-023 B125M-B Patient Monitor 6160002-024 B105M-OR Patient Monitor 6160000-143 B105M-OR Patient Monitor 6160000-144 B155M-OR Patient Monitor 6160000-145

GE Healthcare Finland Oy

Potential loss of monitoring on affected monitors when powered by certain batteries. Affected batteries can lose capability to hold charge and provide back up power. If this situation occurs, it will cause loss of patient monitoring and potentially delay recognizing patient status changes requiring treatment.

September 26, 2025 · DeviceView details →
Class IIOngoing

CARESCAPE ONE, Model no. 2087075-300 - shipped with potentially affected batteries or affected batteries installed as a spare part Monitor, Physiological, Patient (With Arrhythmia Detection or Alarms Updated 3/19 to add CARESCAPE ONE MBZ101 2087075-001

GE Healthcare Finland Oy

Potential loss of monitoring on affected monitors when powered by certain batteries. Affected batteries can lose capability to hold charge and provide back up power. If this situation occurs, it will cause loss of patient monitoring and potentially delay recognizing patient status changes requiring treatment.

September 26, 2025 · DeviceView details →
Class IIOngoing

SAFE-T-FILL Plastic Blood Gas Capillary Tubes, 230 ¿L; Prepared with Sodium Heparin Model/Catalog Number: 06 0009 Product Description: A clear, plastic capillary blood collection tube

ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.

September 26, 2025 · DeviceView details →
Class IOngoing

CODMAN Disposable Perforator 11mm. Cranial Perforator.

Integra LifeSciences Corp. (NeuroSciences)

Expansion of recall of size 14 mm Codman Disposable Perforators for inadequate welds to size 11 mm and 9 mm Codman Disposable Perforators out of an abundance of caution.

September 26, 2025 · DeviceView details →
Class IIOngoing

SAFE-T-FILL Plastic Blood Gas Capillary Tubes, 230 ¿L; Prepared with Balanced Heparin, Model/Catalog Number: 06 0187 Product Description: A clear, plastic capillary blood collection tube

ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.

September 26, 2025 · DeviceView details →
Class IIOngoing

SAFE-T-FILL Micro Capillary Blood Collection, 200 ¿L; Prepared with Sodium Fluoride; Gray Model/Catalog Number: 07 7340 Product Description: The SAFE-T-FILL Capillary Blood Collection System is a collection device used to draw capillary blood from the finger or heelstick.

ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.

September 26, 2025 · DeviceView details →
Class IIOngoing

Brand Name: AART Calf Implant Product Name: Calf Implant Model/Catalog Number: 502-103 - Calf Implant style 1 size 3 UDI-DI code: B490502103 502-104 - Calf Implant style 1 size 4 UDI-DI code: B490502104 502-105 - Calf Implant style 1 size 5 UDI-DI code: B490502105 502-106 - Calf Implant style 1 size 6 UDI-DI code: B490502106 502-201 - Calf Implant style 2 size 1 UDI-DI code: B490502201 502-303 - Calf Implant style 3 size 3 UDI-DI code: B490502303 502-304 - Calf Implant style 3 size 4 UDI-DI code: B490502304

DSAART LLC

Due to manufactured products that deviated from established specifications and being distributed without obtaining the required FDA premarket approvals or clearances.

September 26, 2025 · DeviceView details →
Class IIOngoing

SAFE-T-FILL Micro Capillary Blood Collection, 300 ¿L; Prepared with Lithium Heparin and Plasma Separator Gel; Green Model/Catalog Number: 07 7221 Product Description: The SAFE-T-FILL Capillary Blood Collection System is a collection device used to draw capillary blood from the finger or heelstick.

ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.

September 26, 2025 · DeviceView details →
Class IIOngoing

Zimmer Biomet Dual Mobility Vivacit-E Highly Crosslinked Polyethylene, 28 mm I.D., 44 mm O.D., Size F, Bearing, Model/Catalog Number: 110031012; semi constrained hip prosthesis

Zimmer, Inc.

Zimmer Biomet is conducting a medical device recall for two (2) lots of the Dual Mobility Vivacit-E¿ Bearing due to a commingle. The outer package is labeled as a Size F 44 mm, however, the implant inside the package is a Size G 46 mm, and vice versa.

September 26, 2025 · DeviceView details →
Class IIOngoing

Brand Name: Medistim MiraQ System Product Name: Medistim MiraQ System Model/Catalog Number: MQC04001, MQC14001, MQU14011, MQV12011 Software Version: Not applicable Product Description: Ultrasound device for intraoperative use Component: No

Medistim Asa

Printer Support Module (PSM) may be subject to insufficient soldering, which may cause loosening of the wires and system to shut down. Affected devices need to have their Printer Support Modules replaced.

September 26, 2025 · DeviceView details →
Class IIOngoing

Brand Name: AART Malar Implant Product Name: Malar Implant Model/Catalog Number: 401-202-5 Malar Implant style 2 size 2 left UDI-DI code: B4904012025 401-202-6 Malar Implant style 2 size 2 right UDI-DI code: B4904012026

DSAART LLC

Due to manufactured products that deviated from established specifications and being distributed without obtaining the required FDA premarket approvals or clearances.

September 26, 2025 · DeviceView details →
Class IIOngoing

SAFE-T-FILL Plastic Blood Gas Capillary Tubes, 150 ¿L; Prepared with Sodium Heparin Model/Catalog Number: 06 0007 Product Description: A clear, plastic capillary blood collection tube

ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.

September 26, 2025 · DeviceView details →
Class IIOngoing

Mixing Fleas for SAFE-T-FILL Blood Gas Capillaries, Model 07 9503

ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.

September 26, 2025 · DeviceView details →
Class IIOngoing

SAFE-T-FILL Micro Capillary Blood Collection, 300 ¿L; Prepared with Lithium Heparin; Green Model/Catalog Number: 07 7251 Product Description: The SAFE-T-FILL Capillary Blood Collection System is a collection device used to draw capillary blood from the finger or heelstick.

ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.

September 26, 2025 · DeviceView details →
Class IIOngoing

SAFE-T-FILL Plastic Blood Gas Capillary Tubes, 150 ¿L; Untreated. Model 06 0199 Product Description: A clear, plastic capillary blood collection tube

ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.

September 26, 2025 · DeviceView details →
Class IIOngoing

Portrait VSM Model nos. 6660000-666 Monitor, Physiological, Patient (With Arrhythmia Detection or Alarms

GE Healthcare Finland Oy

Potential loss of monitoring on affected monitors when powered by certain batteries. Affected batteries can lose capability to hold charge and provide back up power. If this situation occurs, it will cause loss of patient monitoring and potentially delay recognizing patient status changes requiring treatment.

September 26, 2025 · DeviceView details →
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