Medical device recalls (page 13)
2545 recalls.
- Medline EBSI Kit EBSI1534 recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Philips Allura Xper with the following Model Numbers: Model # 722001 for Allura Xper FD10C recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported June 24, 2026 · Philips Allura Xper and MultiDiagnost-Eleva systems Hand switch button not fully releasing potentially leading to loss of imaging functionality or unintended ... - Philips MultiDiagnost Eleva with the following Model Numbers: Model # 708032 for... recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported June 24, 2026 · Philips Allura Xper and MultiDiagnost-Eleva systems Hand switch button not fully releasing potentially leading to loss of imaging functionality or unintended ... - Description/REF: RA CATH KIT: 20 GA X 1-1/2IN/NA-04220-1A recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: CVC KIT: 16 GA X 8IN/AK-04210 recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: PICC ACCESS TRAY/ASK-04001-CG1 recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: MIDLINE CATHETER KIT: 3 FR X 20 CM/CDC-02031-MK1A recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: PSI KIT: 7 FR X 4 IN/ASK-09701-UP recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: ACCESS TRAY/ASK-04001-MC3 recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: RA CATH KIT: 20 GA X 1-3/4IN/AK-04020-SPC recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: SAC KIT: 18 GA X 12CM W BIO/SAC-01218-B recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: SPINAL ANESTHESIA KIT/ASA-24090-SB recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: HEMODIALYSIS KIT: 2-LUMEN 12 FR X 20 CM/AK-15122-F recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: PI MIDLINE 2L: 5FR X 20CM/CDC-32052-MPKC recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: PARACENTESIS KIT/ASK-00376-JHH recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: ACCESS TRAY/GU-04020 recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: ACCESS TRAY/ASK-04001-JHH recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: PACING/PSI KIT: 5 FR 2L/ASK-07155-MGU recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: DRAINAGE KIT/AK-01600 recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: HEMODIALYSIS KIT: 2-LUMEN 12 FR X 16 CM/AK-12122-F recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: PERITONEAL LAVAGE CATH KIT:8FR/AK-09000 recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: PI JACC KIT: 2L 5.5 FR X 15 CM CG+/ASK-41552-LTAC recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: PI PICC: 3: 6FR x 55CM w CHG/ DLX-35563-HPKC recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: ARTERIAL LINE KIT: SL 20 GA X 5 IN/ASK-04510-MM6 RA CATH KIT: 20 GA X... recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: CVC/PSI KIT: 2 LUMEN 8 FR X 6 IN/ASK-42802-PLH recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: PI CVC KIT: 3L 7 FR X 16 CM AGB+/ASK-42703-PNHS2 recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: AHDC KIT: 3-L 12 FR X 16 CM/AK-12123-PCDC recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: HEMODIALYSIS KIT: 2-LUMEN 8 FR X 11 CM/AK-11802-F recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: HEMODIALYSIS KIT: 2L 14 FR X 20 CM AGB CDC-25142-X1A recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: EPIDURAL CATHETER KIT: 19 GA X 90 CM/ASK-05502-VM1 recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: PI AGBA PICC KIT: 3L 6 FR X 40 CM W/VPS/ASK-44063-NS AGBA... recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: PSI KIT: 7 FR X 4IN ANTIMICROBIAL/ASK-09701-UMH recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: RA CATH KIT: 20 GA X 1 3/4 IN/TJ-04020-1 recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: AGBA PICC G4 Stylet: 3L 6FR x 55CM BP/DLX-45563-VPSB recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: PACING PSI KIT: 6 FR/AI-06210-KS recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: BIOPSY SYSTEM COMPREHENSIVE KIT/ASK-09458-AH recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: ACCESS TRAY/ASK-04001-SUH-S recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - PARACENTESIS KIT recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Automated Impella Controller recall (Abiomed, Inc.)
Medical deviceClass IReported June 24, 2026 · Potential software error in the Automated Impella Controller ("AIC" ) when used in conjunction with left ventricular Impella devices. - Panda Freestanding Warmer recall (Datex-Ohmeda Inc)
Medical deviceClass IReported June 24, 2026 · Blender knob shaft can loosen, which can affect the delivered oxygen concentration. The system can deliver an oxygen concentration that does not match the... - Giraffe Warmer with Integrated Resuscitation System recall (Datex-Ohmeda Inc)
Medical deviceClass IReported June 24, 2026 · Blender knob shaft can loosen, which can affect the delivered oxygen concentration. The system can deliver an oxygen concentration that does not match the... - Giraffe Stand-alone Infant Resuscitation System recall (Datex-Ohmeda Inc)
Medical deviceClass IReported June 24, 2026 · Blender knob shaft can loosen, which can affect the delivered oxygen concentration. The system can deliver an oxygen concentration that does not match the... - Orca Single Use Air/Water and Suction Valves recall (Boston Scientific Corporation)
Medical deviceClass IIReported June 17, 2026 · Boston Scientific is initiating a medical device removal of Orca Sterile, Single Use Air/Water and Suction Valves due to a higher than anticipated occurrence... - Halyard recall (AVID Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Inadvertent distribution of sealed pouches that had not undergone validated sterilization. - Halyard recall (AVID Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Inadvertent distribution of sealed pouches that had not undergone validated sterilization. - Halyard recall (AVID Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Inadvertent distribution of sealed pouches that had not undergone validated sterilization. - Halyard recall (AVID Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Inadvertent distribution of sealed pouches that had not undergone validated sterilization. - MOSAIQ Oncology Information System recall (Elekta, Inc.)
Medical deviceClass IIReported June 17, 2026 · Software may fail to load adapted baseline shift plan during treatment delivery when a communication error occurs. - Merlin" Patient Care System recall (Abbott Medical)
Medical deviceClass IIReported June 17, 2026 · Software malfunction may occur during pacing capture threshold test of pacemaker resulting in programmer not successfully communicating the command to... - Boston Scientific Model SC-4318 recall (Boston Scientific Neuromodulation Corporation)
Medical deviceClass IIReported June 17, 2026 · Sterile anchors my lack sterility assurance. - Boston Scientific TCN Electrodes: REF: TCN-5 recall (Boston Scientific Neuromodulation Corporation)
Medical deviceClass IIReported June 17, 2026 · Reusable electrodes may not meet expected performance levels. - Boston Scientific CSK Electrodes: REF: CSK-TC10 recall (Boston Scientific Neuromodulation Corporation)
Medical deviceClass IIReported June 17, 2026 · Reusable electrodes may not meet expected performance levels. - Bicarby Dialysate recall (Fresenius Medical Care Holdings, Inc.)
Medical deviceClass IIReported June 17, 2026 · There is an error in the labeling of the GTIN on the product. When scanned; however, the case labeling, lot number, and printed labeling on the product... - Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit recall (Inter-Med Llc)
Medical deviceClass IIReported June 17, 2026 · Some units of Aluminum Chloride Gel contain the package insert for Ferric Sulfate Gel. The incorrect insert misidentifies the product and contains different... - Hintermann Series Talar Implant recall (DT MedTech, LLC)
Medical deviceClass IIReported June 17, 2026 · Through customer complaints, the ankle replacement system was found to contain incorrect devices: Left implant packaging and labeling bears a right implant... - Siemens Dimension Tacrolimus Flex Reagent Cartridge recall (Siemens Healthcare Diagnostics, Inc.)
Medical deviceClass IIReported June 17, 2026 · A potential positive bias in quality control (QC) and patient sample results in three lots of the Dimension Tacrolimus (TAC) Flex reagent cartridge. - Brand Name: EXENT Analyser Product Name: EXENT Analyser Model/Catalog Number:... recall (The Binding Site Group, Ltd.)
Medical deviceClass IIReported June 17, 2026 · It was reported that plates 2 and 3 were marked as passed , although it appeared that QC had not been performed on these plates, despite samples being... - Medartis APTUS recall (Medartis AG)
Medical deviceClass IIReported June 17, 2026 · The cannulation of the CCS screw is not centered. - NexxZr T Multi A3.5 W98-16mm recall (Sagemax Bioceramics, Inc.)
Medical deviceClass IIReported June 17, 2026 · Yttrium-stabilized zirconium oxide discs for fixed all-ceramic dental restorations may have reduced or missing dentin layer and when used clinically in the... - NeoSpan¿ SuperElastic Compression Staple w/Instruments Catalog Number and Product... recall (In2bones USA, LLC)
Medical deviceClass IIReported June 17, 2026 · Due to the Magnetic Resonance Conditional Symbol missing on the carton, inner tray, and patient label. - DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035. recall (Philips North America Llc)
Medical deviceClass IIReported June 17, 2026 · System was delivered without the required Seismic kit for Wall Stand VS2, which is designed to prevent damage and ensure stability of the Wall Stand VS2 during... - SD LTM 64 PLUS recall (Micromed S.p.A.)
Medical deviceClass IIReported June 17, 2026 · Natus has become aware of two complaints related to the SD LTM 64 PLUS where the EEG traces acquired from two or four different amplifiers used in a multiple... - Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit... recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit... recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit... recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit... recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit... recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit... recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 24 Fr PULL ... recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 20 Fr PULL ... recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 14 Fr PULL ... recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 24 Fr PUSH OTW ... recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 20 Fr PUSH OTW ... recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 14 Fr PUSH OTW ... recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: CORFLO Safety PEG Kit with ENFit Connector Model/Catalog Number:... recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-6312 recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-5320 recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-4320 recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-6316 recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-6312 recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Brand Name: CORFLO Product Name: CORFLO Safety PEG Kit Model/Catalog Number: 30-5320 recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Brand Name: CORFLO Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-4320 recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Brand Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE recall (HF Acquisition Co LLC)
Medical deviceClass IIReported June 17, 2026 · Due to incorrect incubation process being performed on product. - Brand Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE recall (HF Acquisition Co LLC)
Medical deviceClass IIReported June 17, 2026 · Due to incorrect incubation process being performed on product. - CGuard¿ Prime Carotid Stent System recall (INSPIREMD Inc)
Medical deviceClass IIReported June 17, 2026 · Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent. - CGuard Prime Carotid Stent System recall (INSPIREMD Inc)
Medical deviceClass IIReported June 17, 2026 · Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent. - Brand Name: CGuard Prime Carotid Stent System recall (INSPIREMD Inc)
Medical deviceClass IIReported June 17, 2026 · Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent. - CGuard Prime Carotid Stent System recall (INSPIREMD Inc)
Medical deviceClass IIReported June 17, 2026 · Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent. - Brand Name: CGuard¿ Prime Carotid Stent System recall (INSPIREMD Inc)
Medical deviceClass IIReported June 17, 2026 · Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent. - Brand Name: CGuard¿ Prime Carotid Stent System recall (INSPIREMD Inc)
Medical deviceClass IIReported June 17, 2026 · Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent. - TDC VELOCE" recall (D.O.R.C. Dutch Opthalmic Research Center Intl B.V.)
Medical deviceClass IIReported June 17, 2026 · An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use. - TDC VELOCE" recall (D.O.R.C. Dutch Opthalmic Research Center Intl B.V.)
Medical deviceClass IIReported June 17, 2026 · An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use. - TDC VELOCE" recall (D.O.R.C. Dutch Opthalmic Research Center Intl B.V.)
Medical deviceClass IIReported June 17, 2026 · An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use. - Bicarby" Dialysate recall (Fresenius Medical Care Holdings, Inc.)
Medical deviceClass IIReported June 17, 2026 · Given the increased number of leaks reported by users, it was determined to be the appropriate course of action to notify users of the potential for the... - EXCOR Pediatric Ventricular Assist Device recall (BERLIN HEART GMBH)
Medical deviceClass IIReported June 17, 2026 · Blood pump inner package expiration date does not match the outer-correct expiration date, which may lead to delays in surgical procedures. - Mahurkar Elite PASS Trays recall (Mozarc Medical US LLC)
Medical deviceClass IIReported June 17, 2026 · The Tegaderm CHG dressing, as specified in product labeling, was missing from certain lots of Mahurkar Elite PASS Trays. - Allia Moveo angiographic X-ray system recall (GE Medical Systems, LLC)
Medical deviceClass IIReported June 17, 2026 · GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead... - Allia IGS Pulse angiographic X-ray system recall (GE Medical Systems, LLC)
Medical deviceClass IIReported June 17, 2026 · GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead... - Allia IGS 7 Pulse angiographic X-ray system recall (GE Medical Systems, LLC)
Medical deviceClass IIReported June 17, 2026 · GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead... - Allia IGS 5 Pulse angiographic X-ray system recall (GE Medical Systems, LLC)
Medical deviceClass IIReported June 17, 2026 · GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead...