Browse Device Recalls

2,817 FDA medical device safety recalls.

FDA Medical Device Recall Enforcement Database

Browse 2,817 FDA medical device recall enforcement actions. Each entry includes the device description, reason for recall, classification (Class I through III based on severity), recalling firm, and distribution details. Use the filters below to search by year, classification, state, or keyword.

Medical Device Recalls

Browse 2,817 FDA device recalls in 2025.

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Date	Product	Reason	Class	Firm
Nov 19, 2025	AMSCO 7053HP Washer/Disinfector Model/Catalog Number: 7053HP Product De...	Wire connected to the electrical box may shift out of its intended position, which may result in ...	Class II	Steris Corporation
Nov 19, 2025	AMSCO 7052HP Washer/Disinfector Model/Catalog Number: 7052HP Product Des...	Wire connected to the electrical box may shift out of its intended position, which may result in ...	Class II	Steris Corporation
Nov 18, 2025	Intelerad InteleShare software, with ProViewer component	Software intended to aid in diagnosing conditions, planning treatments, visualizing anatomical st...	Class II	DICOM Grid, Inc.
Nov 18, 2025	Brand name: AGFA Digital Radiography X- Ray system DR 800 with MUSICA Dynamic...	It is possible to exceed the maximum allowed Air Kerma rate (AKR) of 88mGy/min for pulsed fluoro ...	Class II	AGFA Healthcare Corp.
Nov 18, 2025	Hardware configuration of the BeneVision Central Monitoring System (CMS), mar...	When the Worstation of the BeneVision DMS has a specific hardware configuration, the computer may...	Class II	Mindray DS USA, Inc. dba Mindray North America
Nov 18, 2025	HemosIL SynthAFax. Partial Thromboplastin Time Tests.	Recalled lots were manufactured with double the amount of preservative concentration.	Class III	Instrumentation Laboratory
Nov 17, 2025	Brand Name: Molift Product Name: Molift Mover 300 Model/Catalog Numbers: (1...	A customer experienced that during assembly and load testing of the device, the bolt for mounting...	Class II	ETAC A/S
Nov 17, 2025	Brand Name: Molift Product Name: Molift 2-point sling bars (Accessory to mob...	A customer experienced that during assembly and load testing of the device, the bolt for mounting...	Class II	ETAC A/S
Nov 17, 2025	Da Vinci 5 ASSY, DV5 CONSOLE, IS5000 Model/Catalog Number: 380730 Used...	An error event following the release of a software version for the surgical system that can resul...	Class II	Intuitive Surgical, Inc.
Nov 17, 2025	Orthofix NorthStar OCT Navigation Surgical Technique Guide, and instruments: ...	The NorthStar OCT Navigation Surgical Technique Guide (STG) incorrectly identified both Medtronic...	Class II	SEASPINE ORTHOPEDICS CORPORATION
Nov 17, 2025	Sheathes3D Seamless Viral Barrier, Latex-Free, 7/8"D Tapered to 2.9"W x 11.8"...	Vaginal/rectal ultrasound probe covers with a viral barrier may have product defects, which may r...	Class II	Sheathing Technologies Inc
Nov 17, 2025	Brand Name: Molift Product Name: Molift Mover 205 Model/Catalog Number: (1)...	A customer experienced that during assembly and load testing of the device, the bolt for mounting...	Class II	ETAC A/S
Nov 17, 2025	The Pressio 2 ICP Monitoring System, Model Number PSO-4000; Intracranial Pres...	Customer complaints of Pressio monitor rebooting.	Class II	Sophysa
Nov 17, 2025	Brand Name: Molift Product Name: Molift 4-point sling bars (Accessory to mob...	A customer experienced that during assembly and load testing of the device, the bolt for mounting...	Class II	ETAC A/S
Nov 14, 2025	Brand Name: ShockPulse-SE Lithotripsy System SPL-S Product Name: ShockPulse-...	Ongoing investigations identified additional instances of the device Generator remaining in a bli...	Class II	Olympus Corporation of the Americas
Nov 14, 2025	GE Healthcare Carestation anesthesia system Power Management Board (PMB) Fiel...	Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia Systems containing cer...	Class I	GE Medical Systems China Co., Ltd.
Nov 14, 2025	Halyard, GENERAL LAPAROSCOPY PACK. Catalog Number: VAST018-10.	Potential for incomplete seal on header bag.	Class II	AVID Medical, Inc.
Nov 14, 2025	Brand Name: ShockPulse-SE Lithotripsy System SPL-SR Product Name: ShockPulse...	Ongoing investigations identified additional instances of the device Generator remaining in a bli...	Class II	Olympus Corporation of the Americas
Nov 14, 2025	GE Healthcare Carestation anesthesia system, product number and REF numbers: ...	Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia Systems containing cer...	Class I	GE Medical Systems China Co., Ltd.
Nov 14, 2025	Ivenix Infusion System (IIS), LVP Software LVP-SW-0005. Software for the cont...	Software version 5.10.1 and earlier contain anomalies that have the potential to cause serious pa...	Class I	Fresenius Kabi USA, LLC
Nov 14, 2025	Halyard, HEAD AND NECK TRAY. Catalog Number: EURO016-09.	Potential for incomplete seal on header bag.	Class II	AVID Medical, Inc.
Nov 14, 2025	Halyard, MAJOR PACK. Catalog Number: JEMJ10-01.	Potential for incomplete seal on header bag.	Class II	AVID Medical, Inc.
Nov 14, 2025	GE Healthcare Carestation anesthesia system, product number and REF numbers: ...	Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia Systems containing cer...	Class I	GE Medical Systems China Co., Ltd.
Nov 14, 2025	Halyard, EP LAB PK. Catalog Number: ESJH009-03.	Potential for incomplete seal on header bag.	Class II	AVID Medical, Inc.
Nov 14, 2025	Halyard, MIDTOWN GENERAL ARTERIOGRAM. Catalog Number: EUHM009-01.	Potential for incomplete seal on header bag.	Class II	AVID Medical, Inc.
Nov 14, 2025	Brand Name: ShockPulse-SE Lithotripsy System Product Name: ShockPulse-SE Lit...	Ongoing investigations identified additional instances of the device Generator remaining in a bli...	Class II	Olympus Corporation of the Americas
Nov 13, 2025	FORCEP, STD STR, STERILE KELLY, 5.5 IN, Item Number DYNJ04048	The items may have weak packaging seals that may result in a breach of sterility if the seal fail...	Class II	Medline Industries, LP
Nov 13, 2025	SCISSORS, OR, SHARP/BLUNT, 5.5", STERILE, Item Number DYND04000	The items may have weak packaging seals that may result in a breach of sterility if the seal fail...	Class II	Medline Industries, LP
Nov 13, 2025	InPen App, Model/CFN Number: MMT-8061 (Android Users)	When app is uninstalled and reinstalled, insulin pen software issue causes Choose Notification St...	Class II	Medtronic MiniMed, Inc.
Nov 13, 2025	Alinity ci-series System Control Module (SCM), REF: 03R70-01, 03R70-20	Abbott Laboratories is recalling their Alinity ci-series System Control Module, a chemistry/immun...	Class II	Abbott Laboratories
Nov 13, 2025	KWIK-STIK, Quality control kit for culture media, Vibrio parahaemolyticus der...	Some products packaged for lot 818-111-7 may have been packaged in pouches labeled as lot 857-53-10.	Class II	Microbiologics Inc
Nov 12, 2025	1. CAMHB W/LHB, MANUAL, 11ML, 10/BOX YCP112-10 2. BRUCELLA BROTH, 11ML, 10...	Products may contain contamination, which may result in a darker or brown media color.	Class II	Remel, Inc
Nov 12, 2025	ChemoPlus gowns: Product Code Product Description CT5500T ChemoPlus Full Co...	Affected gowns have the incorrect expiration date on the product packaging. Product has a shelf-l...	Class II	Cardinal Health 200, LLC
Nov 12, 2025	The Stryker CranialMask Tracker is a single-use device consisting of a flexib...	When the device is activated during surgery, the device software issues an error message "Instrum...	Class II	Howmedica Osteonics Corp.
Nov 11, 2025	Olympus Inner Sheath, Long; Model No. WA22017T. Inner sheath for urological ...	Complaints of the ceramic tip of the resection sheath breaking have been received.	Class II	Olympus Corporation of the Americas
Nov 11, 2025	Olympus Inner Sheath. Model No. A2642. for endoscopic diagnosis and treatmen...	Complaints of the ceramic tip of the resection sheath breaking have been received.	Class II	Olympus Corporation of the Americas
Nov 11, 2025	Olympus Resection Sheath. Model No. A22014A and A22014T. for endoscopic diagn...	Complaints of the ceramic tip of the resection sheath breaking have been received.	Class II	Olympus Corporation of the Americas
Nov 11, 2025	Halyard MINI PLUS KIT SOUTH, Kit Code: JACK097-08	Devices are not suitable for organ transplant.	Class I	AVID Medical, Inc.
Nov 11, 2025	DEXLOCK Achilles Repair Implant Kits, MAKT4520	There have been multiple complaints of drill bit fusing to the bushing/sleeve within the drill gu...	Class II	Medline Industries, LP
Nov 11, 2025	Olympus Resection Sheath, 26 Fr.; Model No. A22042A. Resection sheath for uro...	Complaints of the ceramic tip of the resection sheath breaking have been received.	Class II	Olympus Corporation of the Americas
Nov 11, 2025	Olympus Resection Sheath, 24 Fr; Model No. A22041A. Resection sheath for uro...	Complaints of the ceramic tip of the resection sheath breaking have been received.	Class II	Olympus Corporation of the Americas
Nov 11, 2025	Olympus Inner Sheath 21 Fr. Model No. A2660T. for endoscopic diagnosis and t...	Complaints of the ceramic tip of the resection sheath breaking have been received.	Class II	Olympus Corporation of the Americas
Nov 11, 2025	Olympus Resection Sheath. Model No. A2666T. for endoscopic diagnosis and tre...	Complaints of the ceramic tip of the resection sheath breaking have been received.	Class II	Olympus Corporation of the Americas
Nov 11, 2025	Olympus Resection Inner Sheath for 26 Fr. Outer Sheath. Model No. A22040T. R...	Complaints of the ceramic tip of the resection sheath breaking have been received.	Class II	Olympus Corporation of the Americas
Nov 11, 2025	Halyard ORGAN RECOVERY OR PACK, Kit Code: LLOG1000-15.	Devices are not suitable for organ transplant.	Class I	AVID Medical, Inc.
Nov 11, 2025	Olympus Inner Sheath. Model No. A4741. for endoscopic diagnosis and treatmen...	Complaints of the ceramic tip of the resection sheath breaking have been received.	Class II	Olympus Corporation of the Americas
Nov 11, 2025	Halyard ORGAN RECOVERY OR PACK, Kit Code: LLOF1000-17.	Devices are not suitable for organ transplant.	Class I	AVID Medical, Inc.
Nov 11, 2025	Olympus Resection Sheath; Model No. A2666. Resection sheath for urologic appl...	Complaints of the ceramic tip of the resection sheath breaking have been received.	Class II	Olympus Corporation of the Americas
Nov 11, 2025	Olympus Resection Sheath, 8 mm. Model No. A42011A. Resection sheath for gyne...	Complaints of the ceramic tip of the resection sheath breaking have been received.	Class II	Olympus Corporation of the Americas
Nov 11, 2025	Olympus Resection Sheath, 26 Fr. with Deflecting Obturator; Model No. A22042T...	Complaints of the ceramic tip of the resection sheath breaking have been received.	Class II	Olympus Corporation of the Americas

Frequently Asked Questions

When a device safety issue is identified, the manufacturer or FDA initiates a recall. The FDA publishes an enforcement report detailing the device, the reason for the recall, and distribution. Healthcare facilities and providers are notified to check their inventory and take corrective action.

All types — from simple devices like blood glucose test strips and surgical gloves to complex devices like pacemakers, defibrillators, insulin pumps, hip implants, and ventilators. Software-driven devices are increasingly common in recalls due to bugs and cybersecurity vulnerabilities.

Use the search and filter tools on this page. Each recall entry includes the device description, model numbers, and distribution details so you can determine if your device is affected. Contact your healthcare provider if you find a match.