Medical device recalls (page 17)
2545 recalls.
- Medline medical procedure kits recall (Medline Industries, LP)
Medical deviceClass IIReported May 6, 2026 · During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market... - Medline medical procedure kits recall (Medline Industries, LP)
Medical deviceClass IIReported May 6, 2026 · During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market... - Medline medical procedure kits recall (Medline Industries, LP)
Medical deviceClass IIReported May 6, 2026 · During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market... - Medline medical procedure kits recall (Medline Industries, LP)
Medical deviceClass IIReported May 6, 2026 · During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market... - Medline medical procedure kits recall (Medline Industries, LP)
Medical deviceClass IIReported May 6, 2026 · During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market... - Medline Neuro Sponges recall (Medline Industries, LP)
Medical deviceClass IIReported May 6, 2026 · During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market... - Brand Name: Leksell Vantage Arc System REF: 1053958 recall (Elekta, Inc.)
Medical deviceClass IIReported May 6, 2026 · Locking mechanisms may not properly secure to the Arc system, resulting in shifting of coordinates during procedures. - epoc BGEM BUN Test Card recall (Siemens Healthcare Diagnostics Inc)
Medical deviceClass IIReported May 6, 2026 · Use of the affected product can result in discrepant low pH and measured Total Carbon Dioxide (mTCO2) results and corresponding calculated values in arterial... - Philips Bridge Prep Kit REF: K12-09098C Sterile EO recall (Merit Medical Systems, Inc.)
Medical deviceClass IIReported May 6, 2026 · catheter may experience resistance when being advanced over the guidewire - Philips Bridge Prep Kit REF: K12-09098C Sterile EO recall (Merit Medical Systems, Inc.)
Medical deviceClass IIReported May 6, 2026 · catheter may experience resistance when being advanced over the guidewire - Philips Bridge Prep Kit REF: K12-09098B Sterile EO recall (Merit Medical Systems, Inc.)
Medical deviceClass IIReported May 6, 2026 · catheter may experience resistance when being advanced over the guidewire - i-STAT G3+ cartridge recall (Abbott Point Of Care Inc.)
Medical deviceClass IIReported May 6, 2026 · Approximately 7.6% of cartridges from specific i-STAT EG7+ (list number 03P76-25), i-STAT EG6+ (list number 03P77-25) and i-STAT G3+ (list number 03P78-26)... - i-STAT EG6+ cartridge recall (Abbott Point Of Care Inc.)
Medical deviceClass IIReported May 6, 2026 · Approximately 7.6% of cartridges from specific i-STAT EG7+ (list number 03P76-25), i-STAT EG6+ (list number 03P77-25) and i-STAT G3+ (list number 03P78-26)... - i-STAT EG7+ cartridge recall (Abbott Point Of Care Inc.)
Medical deviceClass IIReported May 6, 2026 · Approximately 7.6% of cartridges from specific i-STAT EG7+ (list number 03P76-25), i-STAT EG6+ (list number 03P77-25) and i-STAT G3+ (list number 03P78-26)... - Heraeus recall (Heraeus Medical GmbH (Dental Division))
Medical deviceClass IIIReported May 6, 2026 · Based on long-term stability testing, it was determined that in units older than 1.5 years (17 months) the mixing rod may, in rare cases, come loose from its... - Heraeus recall (Heraeus Medical GmbH (Dental Division))
Medical deviceClass IIIReported May 6, 2026 · Based on long-term stability testing, it was determined that in units older than 1.5 years (17 months) the mixing rod may, in rare cases, come loose from its... - iLet Bionic Pancreas recall (Beta Bionics, Inc.)
Medical deviceClass IIReported May 6, 2026 · insulin pump software versions 1.4.2, and 1.4.3 issue with Dexcom Continuous Glucose Monitoring (CGM) G7 sensor may result in delayed CGM reading then switch... - Straumann n!ce Zr recall (Straumann USA LLC)
Medical deviceClass IIReported May 6, 2026 · Includes an incorrect screw seat interface. - Straumann n!ce PMMA Full-arch Restoration. Screw-retained Bridge. Article 010.0304. ... recall (Straumann USA LLC)
Medical deviceClass IIReported May 6, 2026 · Includes an incorrect screw seat interface. - Depuy Synthes recall (DEPUY (IRELAND))
Medical deviceClass IIReported May 6, 2026 · The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility. - Depuy Synthes recall (DEPUY (IRELAND))
Medical deviceClass IIReported May 6, 2026 · The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility. - Depuy Synthes recall (DEPUY (IRELAND))
Medical deviceClass IIReported May 6, 2026 · The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility. - Depuy Synthes recall (DEPUY (IRELAND))
Medical deviceClass IIReported May 6, 2026 · The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility. - Depuy Synthes recall (DEPUY (IRELAND))
Medical deviceClass IIReported May 6, 2026 · The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility. - Depuy Synthes recall (DEPUY (IRELAND))
Medical deviceClass IIReported May 6, 2026 · The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility. - Depuy Synthes recall (DEPUY (IRELAND))
Medical deviceClass IIReported May 6, 2026 · The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility. - Depuy Synthes recall (DEPUY (IRELAND))
Medical deviceClass IIReported May 6, 2026 · The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility. - Depuy Synthes recall (DEPUY (IRELAND))
Medical deviceClass IIReported May 6, 2026 · The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility. - Immy recall (Immuno-Mycologics, Inc)
Medical deviceClass IIReported May 6, 2026 · Neutralization Buffer may contain contaminants - BD GasPak EZ Campy Pouch System. Catalog Number: 260685. for microbiologic use recall (Becton Dickinson & Co.)
Medical deviceClass IIReported May 6, 2026 · BD identified an issue affecting certain lots of BD GasPak EZ CO2 and BD GasPak EZ Campy Gas Generating Pouch Systems, where gas generating sachets may produce... - BD GasPak EZ CO2 Pouch System. Catalog Number: 260684. for microbiologic use recall (Becton Dickinson & Co.)
Medical deviceClass IIReported May 6, 2026 · BD identified an issue affecting certain lots of BD GasPak EZ CO2 and BD GasPak EZ Campy Gas Generating Pouch Systems, where gas generating sachets may produce... - Dimension Creatinine Flex reagent cartridge. Material Number: 10872079. recall (Siemens Healthcare Diagnostics, Inc.)
Medical deviceClass IIReported May 6, 2026 · Siemens Healthcare Diagnostics is recalling certain lots of Dimension Creatinine Flex reagent cartridge (Dimension CRE2) because a potential imprecision in the... - Philips Upgrade to MR 7700 with MR Elastography recall (Philips North America)
Medical deviceClass IIReported May 6, 2026 · The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading... - Philips SmartPath to Ingenia Elition X with MR Elastography recall (Philips North America)
Medical deviceClass IIReported May 6, 2026 · The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading... - Philips SmartPath to dStream for XR and 3.0T with MR Elastography recall (Philips North America)
Medical deviceClass IIReported May 6, 2026 · The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading... - Philips SmartPath to dStream for 3.0T with MR Elastography recall (Philips North America)
Medical deviceClass IIReported May 6, 2026 · The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading... - Philips SmartPath to dStream for 1.5T with MR Elastography recall (Philips North America)
Medical deviceClass IIReported May 6, 2026 · The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading... - Philips MR 7700 with MR Elastography recall (Philips North America)
Medical deviceClass IIReported May 6, 2026 · The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading... - Philips Ingenia Elition X with MR Elastography recall (Philips North America)
Medical deviceClass IIReported May 6, 2026 · The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading... - Philips Ingenia Elition S with MR Elastography recall (Philips North America)
Medical deviceClass IIReported May 6, 2026 · The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading... - Philips Ingenia Ambition X with MR Elastography recall (Philips North America)
Medical deviceClass IIReported May 6, 2026 · The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading... - Philips Ingenia Ambition S with MR Elastography recall (Philips North America)
Medical deviceClass IIReported May 6, 2026 · The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading... - Philips Ingenia 3.0T CX with MR Elastography recall (Philips North America)
Medical deviceClass IIReported May 6, 2026 · The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading... - Philips Ingenia 3.0T with MR Elastography recall (Philips North America)
Medical deviceClass IIReported May 6, 2026 · The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading... - Philips Ingenia 1.5T CX with MR Elastography recall (Philips North America)
Medical deviceClass IIReported May 6, 2026 · The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading... - Philips Ingenia 1.5T with MR Elastography recall (Philips North America)
Medical deviceClass IIReported May 6, 2026 · The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading... - Philips Evolution upgrade 3.0T with MR Elastography recall (Philips North America)
Medical deviceClass IIReported May 6, 2026 · The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading... - Philips Evolution Upgrade 1.5T with MR Elastography recall (Philips North America)
Medical deviceClass IIReported May 6, 2026 · The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading... - Philips Achieva 3.0T with MR Elastography recall (Philips North America)
Medical deviceClass IIReported May 6, 2026 · The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading... - Philips Achieva 1.5T Initial system with MR Elastography recall (Philips North America)
Medical deviceClass IIReported May 6, 2026 · The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading... - Philips Achieva 1.5T with MR Elastography recall (Philips North America)
Medical deviceClass IIReported May 6, 2026 · The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading... - Brand Name: HiResolution" Bionic Ear System Product Name: M Zn-Air Battery Pak ... recall (Advanced Bionics, LLC)
Medical deviceClass IIReported May 6, 2026 · The non-tamperproof battery door supplied with the sound processor fails to conform to IEC 60601-1-11:2015 by not requiring the use of a tool to replace the... - Brand Name: Genius" Review Station Product Name: Genius" Review Station Display recall (Hologic, Inc)
Medical deviceClass IIReported May 6, 2026 · It was identified that certain devices were being operated outside the validated and FDA-cleared display configuration due to user modification of the... - Medtronic Sphere-9 Catheter recall (Medtronic, Inc.)
Medical deviceClass IIReported May 6, 2026 · Ventricular fibrillation (VF) occurred during radiofrequency (RF) therapy with the Medtronic Sphere-9 catheter in patients who have a Biotronik Implantable... - AIDBAGs are first aid kits of convenience composed of individually labeled devices... recall (North American Rescue LLC.)
Medical deviceClass IReported May 6, 2026 · Kits contain the McKesson TRUE Metrix PRO Professional Monitoring Blood Glucose System that has been recalled for an issue with the software design of the E-5... - Brand Name: Disposable Mixing Bowls with Spatula Product Name: Mixing Bowl and... recall (Zimmer, Inc.)
Medical deviceClass IIReported May 6, 2026 · Ten complaints have been received identifying issues at the time of use related to the package seal, including incomplete seals, wrinkles in the seals or... - Brand Name: Kiwi Omni Vacuum Delivery System Product Name: Kiwi Omni Vacuum Delivery... recall (Clinical Innovations, LLC)
Medical deviceClass IIReported May 6, 2026 · Due to complaints of device breakage at the traction force gauge to handle joint. - VACUUM BAG SU LARGE recall (Milestone S.R.L.)
Medical deviceClass IIReported May 6, 2026 · There is a possibility of reagent leakage from the specimen container. - Mesh Style Tip Protectors CSW-03-2.0 Open-end style CSW-04-4.0 Closed-end style recall (Healthmark Industries Co., Inc.)
Medical deviceClass IIReported May 6, 2026 · Product does not have FDA clearance. - WHILL Model F recall (WHILL, INC.)
Medical deviceClass IReported May 6, 2026 · Cyber vulnerability of BLE communication was found by CISA VDP program. - WHILL Model C2 recall (WHILL, INC.)
Medical deviceClass IReported May 6, 2026 · Cyber vulnerability of BLE communication was found by CISA VDP program. - Boston Scientific Cardiac Resynchronization Therapy recall (Boston Scientific Corporation)
Medical deviceClass IReported May 6, 2026 · Updated software, Brady software maintenance release 6 (SMR6), is now available for the ACCOLADE" family of pacemakers and cardiac resynchronization therapy... - Boston Scientific Pacemaker recall (Boston Scientific Corporation)
Medical deviceClass IReported May 6, 2026 · Updated software, Brady software maintenance release 6 (SMR6), is now available for the ACCOLADE" family of pacemakers and cardiac resynchronization therapy... - Diversatek Healthcare Viper¿ 3-Stage Wire Guided Balloon Dilator recall (Diversatek Healthcare)
Medical deviceClass IIReported April 29, 2026 · The catheter inflation tag attached to the device may contain an incorrect part number with incorrect balloon diameter sizes and inflation pressures for each... - Diversatek Healthcare Viper¿ 3-Stage Wire Guided Balloon Dilator recall (Diversatek Healthcare)
Medical deviceClass IIReported April 29, 2026 · The catheter inflation tag attached to the device may contain an incorrect part number with incorrect balloon diameter sizes and inflation pressures for each... - Diversatek Healthcare Viper¿ 3-Stage Wire Guided Balloon Dilator recall (Diversatek Healthcare)
Medical deviceClass IIReported April 29, 2026 · The catheter inflation tag attached to the device may contain an incorrect part number with incorrect balloon diameter sizes and inflation pressures for each... - Diversatek Healthcare Viper¿ 3-Stage Fixed Wire Balloon Dilator recall (Diversatek Healthcare)
Medical deviceClass IIReported April 29, 2026 · The catheter inflation tag attached to the device may contain an incorrect part number with incorrect balloon diameter sizes and inflation pressures for each... - Protocol Configuration Tool recall (Foundation Medicine, Inc.)
Medical deviceClass IIReported April 29, 2026 · Potential for spontaneous closures of Hamilton HxRunControl software during execution of Autolys protocols after deployment of the PCT software for AutoLys... - LSL Healthcare Wound Closure Tray recall (LSL Healthcare Inc.)
Medical deviceClass IIReported April 29, 2026 · Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility. - LSL Healthcare recall (LSL Healthcare Inc.)
Medical deviceClass IIReported April 29, 2026 · Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility. - LSL Healthcare recall (LSL Healthcare Inc.)
Medical deviceClass IIReported April 29, 2026 · Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility. - LSL Healthcare recall (LSL Healthcare Inc.)
Medical deviceClass IIReported April 29, 2026 · Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility. - LSL Healthcare recall (LSL Healthcare Inc.)
Medical deviceClass IIReported April 29, 2026 · Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility. - LSL Healthcare recall (LSL Healthcare Inc.)
Medical deviceClass IIReported April 29, 2026 · Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility. - Sequencing Agent SEQ0067 recall (Foundation Medicine, Inc.)
Medical deviceClass IIReported April 29, 2026 · Possible increase in phasing, potentially resulting in false-positive BARD1 splice site indel artifact variants - Flamingo Funnel Large recall (SurgiSmoke Solutions)
Medical deviceClass IIReported April 29, 2026 · Certain lots of product were associated with a manufacturing nonconformance involving use of a non-gamma sterilization compatible drape. - Flamingo Funnel Medium recall (SurgiSmoke Solutions)
Medical deviceClass IIReported April 29, 2026 · Certain lots of product were associated with a manufacturing nonconformance involving use of a non-gamma sterilization compatible drape. - Flamingo Funnel Small recall (SurgiSmoke Solutions)
Medical deviceClass IIReported April 29, 2026 · Certain lots of product were associated with a manufacturing nonconformance involving use of a non-gamma sterilization compatible drape. - Oxoid Agglutinating Sera recall (Remel Europe Ltd.)
Medical deviceClass IIReported April 29, 2026 · Affected lots are not performing to IFU criteria showing cross reactions with 2-0 within 60 seconds. Cross-reactivity may result in the misidentification of a... - Access Total T4 Calibrator recall (Beckman Coulter, Inc.)
Medical deviceClass IIReported April 29, 2026 · Beckman Coulter has identified that Access Total T4 Calibrator lots (PN 33805) exhibit a negative bias on DxI 600/800 instruments, with slopes outside product... - Custom Convenience Kits Pre Op Kit - NS recall (Windstone Medical Packaging, Inc.)
Medical deviceClass IIReported April 29, 2026 · The product correction was initiated because B Braun is issuing a voluntary Urgent Medical Device Correction for gravity IV administration sets as well as pump... - Custom Convenience Kits Pre Op Kit - NS recall (Windstone Medical Packaging, Inc.)
Medical deviceClass IIReported April 29, 2026 · The product correction was initiated because B Braun is issuing a voluntary Urgent Medical Device Correction for gravity IV administration sets as well as pump... - Custom Convenience Kits Pre Op Kit - NS recall (Windstone Medical Packaging, Inc.)
Medical deviceClass IIReported April 29, 2026 · The product correction was initiated because B Braun is issuing a voluntary Urgent Medical Device Correction for gravity IV administration sets as well as pump... - Rover Mobile X-ray System Model/Catalog Number: MXU-RV35 and MXU-RV71 recall (Micro-X Ltd.)
Medical deviceClass IIReported April 29, 2026 · X-Ray generator may malfunction resulting in the X-Ray being inoperable. - Arrowg+ard Blue¿ MAC" Two-Lumen Central Venous Access Kit for use with 7.5 - 8 Fr.... recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IIReported April 29, 2026 · Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured - MAC" Two-Lumen Central Venous Access Kit for use with 7.5 - 8 Fr. Catheters REF... recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IIReported April 29, 2026 · Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured - Pressure Injectable Arrowg+ard Blue Plus¿ Four-Lumen CVC Kit REF ASK-45854-PUPM1 UDI... recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IIReported April 29, 2026 · Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured - ARROW recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IIReported April 29, 2026 · Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured - FLEXTIP PLUS EPIDURAL CATHETER recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IIReported April 29, 2026 · Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured - PERCUTANEOUS SHEATH INTRODUCER with 7.5 - 8 Fr. Catheter REF ASK-09903-MGH3 UDI code: recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IIReported April 29, 2026 · Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured - ARROW RADIAL ARTERY CATHETERIZATION KIT REF ASK-04220-UCL1 UDI code: recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IIReported April 29, 2026 · Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured - Arrow Echogenic Introducer Needle REF ASK-04001-BWK2 UDI code: recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IIReported April 29, 2026 · Due to receiving a notice from a supplier that the liquid adhesive were incorrectly manufactured - OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2330. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely. - OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2138. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely. - OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2119. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely. - OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2118. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely. - OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2117. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely. - OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2116. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely. - OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2115. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · XXX - OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2114. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.