Recalls in July 2026
416 recalls.
- Brand Name: VACUETTE Product Name: LH Lithium Heparin Separator Model/Catalog... recall (Greiner Bio-One North America, Inc.)
Medical deviceClass IIReported October 28, 2026 · Lot B26043FM may include EDTA contamination which introduces potassium while chelating calcium in patient samples, leading to falsely elevated potassium (K+)... - JenaValve Trilogy Delivery Catheter recall (Jenavalve Technology Inc.)
Medical deviceClass IIReported October 21, 2026 · Delivery Catheter may have sleeve liner separation that results in difficulty or inability to deploy heart valve device. - JenaValve Trilogy Delivery Catheter recall (Jenavalve Technology Inc.)
Medical deviceClass IIReported October 21, 2026 · Delivery Catheter may have sleeve liner separation that results in difficulty or inability to deploy heart valve device. - JenaValve Trilogy Delivery Catheter recall (Jenavalve Technology Inc.)
Medical deviceClass IIReported October 21, 2026 · Delivery Catheter may have sleeve liner separation that results in difficulty or inability to deploy heart valve device. - Sweet Sensi Elevated Edibles Hybrid Gum Drops - Passion Guava Kush 140mg THC. Product... recall (SWEET SENSI)
FoodClass IIReported October 14, 2026 · Staphylococcus aureus detected in product. - Tri-Immune Boost recall (Centric Compounding LLC)
DrugNot Yet ClassifiedReported October 14, 2026 · Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin. - Biospectra Tris/Tromethamine recall (BioSpectra, Inc.)
DrugClass IIReported October 14, 2026 · Failed stability specifications - Onkos Surgical Inc. My3D Personalized Pelvic Implant recall (Onkos Surgical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Personalized pelvic implants inadvertently mixed up and distributed to incorrect customers. - Onkos Surgical Inc. My3D Personalized Pelvic Implant recall (Onkos Surgical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Personalized pelvic implants inadvertently mixed up and distributed to incorrect customers. - Sperm Ab ELISA recall (DRG International, Inc.)
Medical deviceClass IIReported October 14, 2026 · Potential for false negative patient results. - Brand Name: ADAPTABLE Beach Chair Product Name: Beach Chair surgical patient... recall (QUANTUM OPS Inc)
Medical deviceClass IIReported October 14, 2026 · Due to a manufacturing issue (inadequate weld) for patient head positioning system. - Generic Name: Kit recall (Medical Action Industries, Inc. 306)
Medical deviceClass IIIReported October 14, 2026 · An internal data-entry error caused kit lot 333606 to be labeled with an expiration date of March 31, 2027, instead of February 28, 2027. - Khazana The Treasure Spice Magic Fennel Candy recall (SLT Foods Inc.)
FoodClass IIReported October 7, 2026 · Undeclared Yellow 5 & 6, Red 3, and Blue 1 - Brand Name: Penumbra System recall (Penumbra Inc.)
Medical deviceClass IIReported October 7, 2026 · Due to manufacturing issues reperfusion catheters may fracture. - Brand Name: Tandem t:slim mobile application Product Name: t:slim Mobile Application recall (Tandem Diabetes Care, Inc.)
Medical deviceClass IIReported October 7, 2026 · A beta (early-release) version of the iOS application, version 2.13 (TestFlight) had a software issue preventing successful pairing of the t:slim application... - Brand Name: Quantum PureFlow Product Name: Quantum PureFlow Standard Heat Exchanger... recall (SPECTRUM MEDICAL SRL)
Medical deviceClass IIReported October 7, 2026 · Due to blood-to-glycol leak in the heat exchanger. - Brand Name: Quantum PureFlow Product Name: Quantum PureFlow Standard Heat Exchanger... recall (SPECTRUM MEDICAL SRL)
Medical deviceClass IIReported October 7, 2026 · Due to blood-to-glycol leak in the heat exchanger. - HeartSine samaritan PAD recall (HeartSine Technologies Ltd)
Medical deviceClass IIIReported October 7, 2026 · Products were distributed without the required Maintenance Supplement, which describes an extra check every 3 months in addition to the monthly check. - Pecorino Toscano D.O.P. STAGIONATO cheese wheels. Product of Italy. Each cheese... recall (Elegant Foods, LLC)
FoodClass IIReported September 30, 2026 · Potential Listeria contamination from dripping condensation in cooler. - Halyard IV START KIT NON-STERILE recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 30, 2026 · Convenience kits containing BD ChloraPrep Clear - 1 mL Applicator, which may exhibit an open or incomplete seal on the packaging of the applicator. - Halyard IV START KIT NON-STERILE recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 30, 2026 · Convenience kits containing BD ChloraPrep Clear - 1 mL Applicator, which may exhibit an open or incomplete seal on the packaging of the applicator. - New York Embroidery Studio Trinity Non-Surgical Isolation Gown recall (New York Embroidery Studio, Inc.)
Medical deviceClass IIReported September 30, 2026 · Gowns do not consistently meet the minimum liquid-barrier performance required. - VITEK 2 AST-N461 TEST KIT recall (Biomerieux Inc)
Medical deviceClass IIReported September 30, 2026 · The issue is related to card pouch damage associated with a portion of the lot which was produced on a specific card pouching device, in a specific timeframe... - CombiSet Hemodialysis Blood Tubing Set with Attached Priming Set and Transducer Protectors recall (Fresenius Medical Care Renal Therapies Group, LLC)
Medical deviceClass IIReported September 30, 2026 · Communication to recommend reviewing the IFU and ensuring that all treatment preparation and handling steps are performed as instructed. - REF: HF2POSTD HomeFill Oxygen System HomeFill cylinder D with CGA870 Compatible Post... recall (Ventec Life Systems, Inc.)
Medical deviceClass IIReported September 30, 2026 · Labeling; Oxygen Cylinders do not contain required medical gas labeling - REF:HF2PC9 HomeFill Oxygen System recall (Ventec Life Systems, Inc.)
Medical deviceClass IIReported September 30, 2026 · Labeling; Oxygen Cylinders do not contain required medical gas labeling - HF2P0ST9 HomeFill Oxygen System HomeFill Cylinder M9 with CGA870 Compatible Post Valve recall (Ventec Life Systems, Inc.)
Medical deviceClass IIReported September 30, 2026 · Labeling; Oxygen Cylinders do not contain required medical gas labeling - Halyard IV START KIT NON-STERILE recall (AVID Medical, Inc.)
Medical deviceClass IReported September 30, 2026 · Convenience kits containing BD ChloraPrep Clear - 1 mL Applicator, which may be contaminated with Aspergillus penicillioides. - Elegant Foods Carrot Cake recall (Elegant Foods, LLC)
FoodClass IIReported September 23, 2026 · Carrot decoration contains Yellow #5 and Yellow #6 which is not listed on finished product label. - Elegant Foods Golden Raisins recall (Elegant Foods, LLC)
FoodClass IIReported September 23, 2026 · Undeclared sulfites - Elegant Foods Coconut Flakes recall (Elegant Foods, LLC)
FoodClass IIReported September 23, 2026 · Undeclared sulfites - Buckhead recall (Buckhead Meat Company D.B.A. Trinity Seafood)
FoodClass IIReported September 23, 2026 · The Firm was notified by NJ Department of Health of two samples collected from tuna with reported high levels of scombrotoxin. - Pi-Cardia Inc. ShortCut REF: Z-A-20.003-US recall (PI CARDIA LTD)
Medical deviceClass IIReported September 23, 2026 · Transfemoral catheter, positing arm may detached due to weld issue. - Reign Medical Clench Staple System recall (F & A Foundation)
Medical deviceClass IIReported September 23, 2026 · Bone fixation staple requires a new 510(k); the performance characteristics of this device have not been adequately established. - Convenience kits CATARACT PACK DYNJ59881A recall (Medline Industries, LP)
Medical deviceClass IIReported September 23, 2026 · Kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to... - Convenience kits MYRINGOTOMY PACK-LF DYNJ59097A recall (Medline Industries, LP)
Medical deviceClass IIReported September 23, 2026 · Kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to... - Convenience kits MINOR PACK DYNJ58421A SPRINGHILL MINOR PACK DYNJ40734F recall (Medline Industries, LP)
Medical deviceClass IIReported September 23, 2026 · Kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to... - Convenience kits ANESTHESIA PAIN PK LEAGUE DYNJ67925A recall (Medline Industries, LP)
Medical deviceClass IIReported September 23, 2026 · Kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to... - SCORPIO C-DOME PATELLA 73-2710 73-2910 SCORPIO U-DOME PATELLA 73-3110 ... recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported September 23, 2026 · Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential... - SCORPIO + MOBILE BEARING PCS 78-5-0910 SYSTEM ONE BIPOLAR 40MM 6074-4022 ... recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported September 23, 2026 · Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential... - TRIDENT 0¿ POLY INSERT 28mm ID 620-00-28D Orthopaedic implant components... recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported September 23, 2026 · Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential... - SCORPIO RECESSED METAL BACKED PATELLA 3045-0026 3045-0028 3045-0030 3045-0032... recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported September 23, 2026 · Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential... - BEARING AND AXLE BUSHING ASSY STD ELBOW C-M113-1-301 KRH REV TIB INS 16mm THK... recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported September 23, 2026 · Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential... - ACETABULAR CUP UHMWPE 61-3258 ALL POLY CONSTRAINED INSERT 44MM 69-2244 ... recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported September 23, 2026 · Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential... - DURACON XL ANGLED TIB INS 11/14MM C-M064-1-300 SELF-PRESSURIZING GLENOID SIZE... recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported September 23, 2026 · Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential... - ABG I ACETABULAR INSERT HOODED 28mm ID X 48mm C-M079-2-801 ARC2F ACETABULAR... recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported September 23, 2026 · Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential... - TRIATHLON HINGE INSERT SIZE 4 11MM 5612-P-411 TRIATHLON HINGE INSERT SIZE 4... recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported September 23, 2026 · Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential... - ALL POLY CONSTRAINED INSERT 54MM 69-2854 NRG KNEE CR 82-2-0512 82-2-0518 ... recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported September 23, 2026 · Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential... - OMNIFIT SERIES I ACET. INSERT 10¿ 22mm ID Catalog No. 2001-2246 Orthopaedic... recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported September 23, 2026 · Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential... - AXLE PIN ASSY LARGE ELBOW COBALT CHROME Catalog No. C-M112-2-500 Orthopaedic... recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported September 23, 2026 · Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential... - Captus 4000e Thyroid Uptake System recall (Mirion Technologies (Capintec), Inc.)
Medical deviceClass IIReported September 23, 2026 · Potential for failure of the tension bolt which would allow the spring arm to unexpectedly fall to its lowest position, which is approximately 25 inches (63.5... - Et Control recall (Datex-Ohmeda, Inc.)
Medical deviceClass IIReported September 23, 2026 · Anesthesia Delivery Systems containing certain electronic gas mixer assemblies can automatically transition to Alternate O2 control. In Alternate O2 control... - Aisys CS2 with Et Control recall (Datex-Ohmeda, Inc.)
Medical deviceClass IIReported September 23, 2026 · Anesthesia Delivery Systems containing certain electronic gas mixer assemblies can automatically transition to Alternate O2 control. In Alternate O2 control... - Aisys CS2 recall (Datex-Ohmeda, Inc.)
Medical deviceClass IIReported September 23, 2026 · Anesthesia Delivery Systems containing certain electronic gas mixer assemblies can automatically transition to Alternate O2 control. In Alternate O2 control... - Aisys recall (Datex-Ohmeda, Inc.)
Medical deviceClass IIReported September 23, 2026 · Anesthesia Delivery Systems containing certain electronic gas mixer assemblies can automatically transition to Alternate O2 control. In Alternate O2 control... - Boston Scientific Corporation StoneSmart Connect Console Contents: recall (Boston Scientific Corporation)
Medical deviceClass IIReported September 23, 2026 · A subset of power adapters used with the connect console may exhibit higher-than-expected resistance in the electrical grounding path. As a result, the power... - Blood Culture Collection Venipuncture Kit 20/Cs recall (Medical Action Industries, Inc. 306)
Medical deviceClass IIReported September 23, 2026 · Blood culture convenience kits contain a component subject to a drug recall that due to an an open or incomplete seal on the packaging of the applicator may... - Kinos Axiom Total Ankle System with Axiom PSR recall (restor3d Inc.)
Medical deviceClass IIReported September 23, 2026 · Ankle implantation systems were packaged with incorrect patient-specific cutting guides, which may result in: delayed surgery, the need to use standard... - SunMed Tracheal Tube recall (WELL LEAD MEDICAL CO. LTD)
Medical deviceClass IIReported September 23, 2026 · The 6Fr suction catheter could not pass through the samples smoothly. - Core Services Hub V8 recall (GE Healthcare)
Medical deviceClass IIReported September 23, 2026 · Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs... - Workflow Core Services V8 recall (GE Healthcare)
Medical deviceClass IIReported September 23, 2026 · Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs... - Centricity PACS Server V7 recall (GE Healthcare)
Medical deviceClass IIReported September 23, 2026 · Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs... - Centricity PACS V2 recall (GE Healthcare)
Medical deviceClass IIReported September 23, 2026 · Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs... - Enterprise Archive V8 recall (GE Healthcare)
Medical deviceClass IIReported September 23, 2026 · Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs... - Centricity Enterprise Archive V2 recall (GE Healthcare)
Medical deviceClass IIReported September 23, 2026 · Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs... - MEDRAD¿ Stellant FLEX Syringe Kit used with Stellant FLEX CT Injection System recall (Bayer Medical Care, Inc.)
Medical deviceClass IIReported September 23, 2026 · Some devices may not have been properly sterilized due to a manufacturing sterilization issue. - Percutaneous Insertion Kit recall (Maquet Cardiopulmonary Gmbh)
Medical deviceClass IIReported September 23, 2026 · The packaging may not consistently maintain sterile barrier integrity. - Percutaneous Insertion Kit recall (Maquet Cardiopulmonary Gmbh)
Medical deviceClass IIReported September 23, 2026 · The packaging may not consistently maintain sterile barrier integrity. - Percutaneous Insertion Kit recall (Maquet Cardiopulmonary Gmbh)
Medical deviceClass IIReported September 23, 2026 · The packaging may not consistently maintain sterile barrier integrity. - Carescape Central Station CSCS V3 MAS800 Desktop Part Number 5867474-04 recall (GE Medical Systems Information Technologies Inc)
Medical deviceClass IIReported September 23, 2026 · Device may not resume patient monitoring for at least 3 minutes following system restart. Issue can lead to potential delay in recognition of clinically... - Philips PIC iX Essentials REF:867093 recall (Philips North America)
Medical deviceClass IIReported September 23, 2026 · Due to software malfunction, patient information system may freeze and become unresponsive. - Philips Patient Information Center iX REF:866389 recall (Philips North America)
Medical deviceClass IIReported September 23, 2026 · Due to software malfunction, patient information system may freeze and become unresponsive. - Medline Convenience Kit: OPEN HEART A PACK recall (Medline Industries, LP)
Medical deviceClass IIReported September 23, 2026 · The kits contain a Retrograde Coronary Sinus Perfusion (RCSP) cannulae that has the potential for a sterile barrier breach. Sterility of the product cannot be... - StatStrip Glucose and B- Ketone meter. Model No: 66429. Glucose test system. recall (Nova Biomedical Corporation)
Medical deviceClass IReported September 23, 2026 · A software synchronization/timing issue in the barcode scanning and patient data processing component that causes the device to intermittently retain a... - StatStrip Glucose and B- Ketone meter. Model No: 63910. Glucose test system. recall (Nova Biomedical Corporation)
Medical deviceClass IReported September 23, 2026 · A software synchronization/timing issue in the barcode scanning and patient data processing component that causes the device to intermittently retain a... - StatStrip Glucose and B- Ketone meter. Model No: 63683. Glucose test system. recall (Nova Biomedical Corporation)
Medical deviceClass IReported September 23, 2026 · A software synchronization/timing issue in the barcode scanning and patient data processing component that causes the device to intermittently retain a... - StatStrip Glucose Hospital Meter System. Model No: 66739. Glucose test system. recall (Nova Biomedical Corporation)
Medical deviceClass IReported September 23, 2026 · A software synchronization/timing issue in the barcode scanning and patient data processing component that causes the device to intermittently retain a... - StatStrip Glucose Hospital Meter System. Model No: 63685. Glucose test system. recall (Nova Biomedical Corporation)
Medical deviceClass IReported September 23, 2026 · A software synchronization/timing issue in the barcode scanning and patient data processing component that causes the device to intermittently retain a... - Halyard IV START KIT NON-STERILE REF: KRIV26-02 recall (AVID Medical, Inc.)
Medical deviceClass IReported September 23, 2026 · Convenience kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which are contaminated with Aspergillus penicillioides - AMS Convenience Kit: DSAEK Pack - RX recall (Windstone Medical Packaging, Inc.)
Medical deviceClass IIReported September 16, 2026 · The convenience kits contain .0.9% Sodium Chloride Injection, USP products in Single Dose freeflex bags, which may contain blue Break-off-Parts (BOPs) that... - HeartSine SAM 350P 350P US Device recall (HeartSine Technologies Ltd)
Medical deviceClass IIReported September 16, 2026 · Due to a damaged (over stretched) membrane tail that causes an intermittent fault. - Halyard IV Start Kit Non-Sterile REF: KRIV26-02 recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 16, 2026 · Convenience kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which lacks sterility assurance due to to wrinkles in the paper... - Kit: Single Shot Epidural 20/Cs recall (Medical Action Industries, Inc. 306)
Medical deviceClass IReported September 16, 2026 · Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility. - Kit: Epidural/Pain TQC 20/Cs recall (Medical Action Industries, Inc. 306)
Medical deviceClass IReported September 16, 2026 · Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility. - OLA-OLA Pounded Yam recall (Fayus Inc.)
FoodClass IReported September 9, 2026 · Undeclared milk. - Bread Pudding with Vanilla Sauce - KIT recall (Ukrop's Homestyle Foods LLC)
FoodClass IIReported September 9, 2026 · Foreign object: metal fragments - Bread Pudding with Vanilla Sauce recall (Ukrop's Homestyle Foods LLC)
FoodClass IIReported September 9, 2026 · Foreign object: metal fragments - Wonton Specialist Inc. Cooked Noodle recall (Wonton Specialists)
FoodClass IIIReported September 9, 2026 · Undeclared FD&C Red No. 40 - Wonton Specialist Inc. Dumpling Skin recall (Wonton Specialists)
FoodClass IIIReported September 9, 2026 · Undeclared FD&C Red No. 40 - Wonton Specialist Inc. Wonton Skin recall (Wonton Specialists)
FoodClass IIIReported September 9, 2026 · Undeclared FD&C Red No. 40 - Wonton Specialist Inc. Lo Mein Noodle recall (Wonton Specialists)
FoodClass IIIReported September 9, 2026 · Undeclared FD&C Red No. 40 - Wonton Specialist Inc. Wonton Noodle recall (Wonton Specialists)
FoodClass IIIReported September 9, 2026 · Undeclared FD&C Red No. 40 - Wonton Specialist Inc. Pan Fried Noodle recall (Wonton Specialists)
FoodClass IIIReported September 9, 2026 · Undeclared FD&C Red No. 40 - Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays:... recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported September 9, 2026 · The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a... - Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays:... recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported September 9, 2026 · The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a... - Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays:... recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported September 9, 2026 · The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a... - Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays:... recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported September 9, 2026 · The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a... - Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays:... recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported September 9, 2026 · The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a... - Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays:... recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported September 9, 2026 · The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a... - Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays:... recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported September 9, 2026 · The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a...