Recalls in July 2026 (page 2)
416 recalls.
- 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... - Citrasate recall (Fresenius Medical Care Renal Therapies Group, LLC)
Medical deviceClass IIReported September 9, 2026 · Complaints of blue-green discoloration in product - NaturaLyte recall (Fresenius Medical Care Renal Therapies Group, LLC)
Medical deviceClass IIReported September 9, 2026 · Complaints of blue-green discoloration in product - GRANUFLO Dry Acid Concentrate: Product Numbers: 0FD2251-3B recall (Fresenius Medical Care Renal Therapies Group, LLC)
Medical deviceClass IIReported September 9, 2026 · Complaints of blue-green discoloration in product - Velys Enabling Tech Robotic-Assist Station REF: 451611001 recall (Medos International Sarl)
Medical deviceClass IIReported September 9, 2026 · Software issue within robotic controller which may cause unintended movement of the robotic arm during bone preparation or instrument positioning. - Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators ORTHO... recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or... - Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators CATARACT... recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or... - Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators C-SECTION... recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or... - Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators LABOR... recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or... - Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators PATIENT... recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or... - Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators DELUXE... recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or... - Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators ADULT... recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or... - Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators BLOOD... recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or... - Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators IV START... recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or... - Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators BLOOD... recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or... - Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators BASIN... recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or... - Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators OPEN... recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or... - Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators PAIN PRE... recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or... - HEALON EndoCoat PRO recall (Johnson & Johnson Surgical Vision, Inc.)
Medical deviceClass IIReported September 9, 2026 · Surgical instructions sent for viscoelastic products used during ophthalmic viscosurgical cataract procedures including in part: If resistance is encountered... - STA Staclot Protein S recall (Diagnostica Stago, Inc.)
Medical deviceClass IIReported September 9, 2026 · A positive drift in QC values within the reagent's stated 4-hour onboard stability period was identified - ERIDANOUS GREEK STYLE Shortbread Cookies with apricot filling and cocoa topping with... recall (Lidl US TRADING)
FoodClass IIReported September 2, 2026 · The firm discovered that certain units shipped to the U.S. retail stores only has "foreign languages" on the label. Product has undeclared wheat, soy, milk... - ERIDANOUS GREEK STYLE Shortbread Cookies with Chocolate Truffle Coating & Apricot... recall (Lidl US TRADING)
FoodClass IIReported September 2, 2026 · The firm discovered that certain units shipped to the U.S. retail stores only has "foreign languages" on the label. Product has undeclared wheat, soy, milk... - bettergoods brand Pistachio Nut Butter recall (Botticelli Foods, LLC)
FoodClass IReported September 2, 2026 · Product may be contaminated with Salmonella. - BLACK AND WHITE GLUTINOUS RICE BALLS WITH BLACK SESAME FILLING recall (KHONG GUAN (HQ))
FoodClass IReported September 2, 2026 · Undeclared peanuts. - Glutinous Rice Balls with Black Sesame Filling recall (KHONG GUAN (HQ))
FoodClass IReported September 2, 2026 · Undeclared peanuts. - FRU recall (GE Medical Systems Information Technologies Inc)
Medical deviceClass IIReported September 2, 2026 · Software issue may result in a loss of patient monitoring at the Hub and Central Viewer. In addition, all alarm settings could be reset to factory defaults... - PORTRAIT CORE SERVICES SOFTWARE V1.0.5 recall (GE Medical Systems Information Technologies Inc)
Medical deviceClass IIReported September 2, 2026 · Software issue may result in a loss of patient monitoring at the Hub and Central Viewer. In addition, all alarm settings could be reset to factory defaults... - PORTRAIT COMPUTE AND CORE SERVICES V1.2 recall (GE Medical Systems Information Technologies Inc)
Medical deviceClass IIReported September 2, 2026 · Software issue may result in a loss of patient monitoring at the Hub and Central Viewer. In addition, all alarm settings could be reset to factory defaults... - PORTRAIT CORE SERVICES SOFTWARE V1.1 recall (GE Medical Systems Information Technologies Inc)
Medical deviceClass IIReported September 2, 2026 · Software issue may result in a loss of patient monitoring at the Hub and Central Viewer. In addition, all alarm settings could be reset to factory defaults... - healthmark ProChek-W Protein Test for Robotic Arms recall (Healthmark Industries Co., Inc.)
Medical deviceClass IIReported September 2, 2026 · Test manufactured with an expired ingredient which may present as either a false negative or positive. - healthmark ProChek-II recall (Healthmark Industries Co., Inc.)
Medical deviceClass IIReported September 2, 2026 · Test manufactured with an expired ingredient which may present as either a false negative or positive. - FUJIFILM Synapse PACS software v7.4.310 recall (FUJIFILM Healthcare Americas Corporation)
Medical deviceClass IIReported September 2, 2026 · Software issue may cause the ruler measurement to be inaccurate. - Medline convenience kits labeled as: 1) LAMI FUSION recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Kits contain a potentially contaminated component which were recalled by the manufacturer - Medline convenience kits labeled as: 1) CMH LITHO MINOR PACK-LF recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Kits contain a potentially contaminated component which were recalled by the manufacturer - Medline convenience kits labeled as: 1) LAVH recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Kits contain a potentially contaminated component which were recalled by the manufacturer - Medline convenience kits labeled as: 1) C-SECTION recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Kits contain a potentially contaminated component which were recalled by the manufacturer - Medline convenience kits labeled as: 1) GYN ROBOTIC CDS recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Kits contain a potentially contaminated component which were recalled by the manufacturer - Medline convenience kits labeled as: 1) MAJOR GYN PACK recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Kits contain a potentially contaminated component which were recalled by the manufacturer - Medline convenience kits labeled as: LTP CDS-LF recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Kits contain a potentially contaminated component which were recalled by the manufacturer - Medline convenience kits labeled as: 1) MAJOR PROCEDURE recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Kits contain a potentially contaminated component which were recalled by the manufacturer - Medline convenience kits labeled as: MAJOR HEAD AND NECK PPS recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Kits contain a potentially contaminated component which were recalled by the manufacturer - Medline convenience kits labeled as: 1) OPEN HEART PACK recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Kits contain a potentially contaminated component which were recalled by the manufacturer - Medline convenience kits labeled as: 1) FEMORAL PACK recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Kits contain a potentially contaminated component which were recalled by the manufacturer - CONMED Linvatec GENESYS CrossFT Suture Anchor with Disposable Driver REF# CFBC-5502B... recall (ConMed Corporation)
Medical deviceClass IIReported September 2, 2026 · Suture anchor may contain incorrect patient implant card which may result in incorrect device identification and traceability. - Grandio Universal Nano-Hybrid Restorative Material - Capsules 0.25Gm recall (Henry Schein Inc.)
Medical deviceClass IIReported September 2, 2026 · Specific lots were distributed in the US with incorrect packaging and Instructions for Use (IFU) from the U.S. FDA-cleared device. - Structur 2 SC Temporary Resin Cartridge Refill 75Gm recall (Henry Schein Inc.)
Medical deviceClass IIReported September 2, 2026 · Specific lots were distributed in the US with incorrect packaging and Instructions for Use (IFU) from the U.S. FDA-cleared device. - Midmark Digital ECG HD+12 recall (Midmark Corporation)
Medical deviceClass IIReported September 2, 2026 · A communication anomoly may result in incorrect electrocardiogram waveforms of a patient and an inaccurate beats-per-minute calculation. - Midmark IQecg Digital ECG recall (Midmark Corporation)
Medical deviceClass IIReported September 2, 2026 · A communication anomoly may result in incorrect electrocardiogram waveforms of a patient and an inaccurate beats-per-minute calculation. - Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03 recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 2, 2026 · Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex. - Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03 recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 2, 2026 · Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex. - Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03 recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 2, 2026 · Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex. - Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03 recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 2, 2026 · Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex. - Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03 recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 2, 2026 · Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex. - Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03 recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 2, 2026 · Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex. - Brand Name: Halyard Product Name: DAVINCI TRUCUSTOM BUNDLE containing TRAY FOLEY... recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 2, 2026 · Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex. - Merge PACS and Merge OrthoPACS recall (Merge Healthcare, Inc.)
Medical deviceClass IIReported September 2, 2026 · Software issue may cause measurements to be displayed inaccurately. - Medline medical convenience kit labeled as: TRACH TUBE KIT recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Component labeling discrepancy - Onli 17cm Hydrophilic Urethral Intermittent Catheter recall (Hollister Ulc)
Medical deviceClass IIReported September 2, 2026 · Hollister has identified that select lots of the catheters identified in the above table may exhibit a protrusion caused by a manufacturing defect which might... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Specific item(s) and lot(s) of Medline convenience kits containing Pilling Wecksorb Neurosponges and Neurosponge Strips are being recalled due to potential... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Specific item(s) and lot(s) of Medline convenience kits containing Pilling Wecksorb Neurosponges and Neurosponge Strips are being recalled due to potential... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Specific item(s) and lot(s) of Medline convenience kits containing Pilling Wecksorb Neurosponges and Neurosponge Strips are being recalled due to potential... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Specific item(s) and lot(s) of Medline convenience kits containing Pilling Wecksorb Neurosponges and Neurosponge Strips are being recalled due to potential... - Medline breathing circuits labeled as: 1) MEDLINE HUDSON RCI recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Neonatal and infant heated wire breathing circuits may experience sporadic failure. The heated wire connector (pigtail) at the humidifier may exhibit... - Medline breathing circuits labeled as: 1) HUDSON RCI recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Neonatal and infant heated wire breathing circuits may experience sporadic failure. The heated wire connector (pigtail) at the humidifier may exhibit... - Medline Hudson RCI recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Neonatal and infant heated wire breathing circuits may experience sporadic failure. The heated wire connector (pigtail) at the humidifier may exhibit... - Jalapeno Pepper packaged in bulk generic Coast Tropical cardboard packaging. Packaged... recall (Coast Citrus Distributors)
FoodClass IReported August 26, 2026 · Potential Salmonella Javiana contamination - Prospector Popcorn Belgian Chocolate Toffee Gourmet Popcorn 3.5oz recall (Prospector Popcorn, LLC)
FoodClass IIIReported August 26, 2026 · Inaccurately declared nutrients including Iron (understated), and Vitamin D (overstated). - Prospector Popcorn Fudge Brownie Gourmet Popcorn 1.5oz and 3.5oz recall (Prospector Popcorn, LLC)
FoodClass IIIReported August 26, 2026 · Inaccurately declared nutrients including Potassium (overstated) and Calcium (overstated). - Prospector Popcorn Maple Walnut Ice Cream Gourmet Popcorn 3.5 oz. recall (Prospector Popcorn, LLC)
FoodClass IIIReported August 26, 2026 · Inaccurately declared nutrients including Potassium (overstated), Calcium (overstated), and Iron (understated). - Prospector Popcorn Chocolate Mocha Gourmet Popcorn 1.5 oz. recall (Prospector Popcorn, LLC)
FoodClass IIReported August 26, 2026 · Inaccurately declared nutrients including Carbohydrates (understated) and Cholesterol (understated). - niCARdipine Hydrochloride Injection recall (American Regent, Inc.)
DrugClass IIReported August 26, 2026 · Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde - Tralement recall (American Regent, Inc.)
DrugClass IIReported August 26, 2026 · Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde - Papaverine HCl Injection recall (American Regent, Inc.)
DrugClass IReported August 26, 2026 · Presence of Particulate Matter: Product contaminated with particulate matter identified as glass and/or paraformaldehyde - Multrys recall (American Regent, Inc.)
DrugClass IIReported August 26, 2026 · Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde - Selenious Acid Injection recall (American Regent, Inc.)
DrugClass IIReported August 26, 2026 · Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde - ACETYLCYSTEINE SOLUTION recall (American Regent, Inc.)
DrugClass IIReported August 26, 2026 · Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde - ACETYLCYSTEINE SOLUTION recall (American Regent, Inc.)
DrugClass IIReported August 26, 2026 · Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde - Atropine Sulfate injection recall (American Regent, Inc.)
DrugClass IIReported August 26, 2026 · Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde - AMINAOCAPROIC ACID INJECTION recall (American Regent, Inc.)
DrugClass IIReported August 26, 2026 · Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde - Cyanocobalamin injection USP recall (American Regent, Inc.)
DrugClass IIReported August 26, 2026 · Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde - Cyanocobalamin injection USP recall (American Regent, Inc.)
DrugClass IIReported August 26, 2026 · Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde - Nitroglycerin injection recall (American Regent, Inc.)
DrugClass IIReported August 26, 2026 · Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde - Acamprosate Calcium recall (Mylan Pharmaceuticals Inc)
DrugClass IIReported August 26, 2026 · Failed Dissolution Specifications - Libtayo recall (Regeneron Pharmaceuticals Inc)
DrugClass IIReported August 26, 2026 · Lack of Assurance of Sterility - PEMRYDI RTU recall (Shilpa Medicare Limited)
DrugClass IIReported August 26, 2026 · Discolored solution. The firm has received market complaints reporting green to dark green discoloration in certain vials - PEMRYDI RTU recall (Shilpa Medicare Limited)
DrugClass IIReported August 26, 2026 · Discolored solution. The firm has received market complaints reporting green to dark green discoloration in certain vials - Esteem Body Soft Convex Urostomy Pouch Model/Catalog Numbers: 423703 recall (ConvaTec, Inc)
Medical deviceClass IIReported August 26, 2026 · Urostomy Pouches may leak from cap during use. - Fort Defiance Industries recall (Fort Defiance Industries, LLC)
Medical deviceClass IIReported August 26, 2026 · The Automated Field Steam Sterilizer's water recovery system 120V Amphenol connector may experience an intermittent loss of ground continuity, which could... - MiniMed 780G Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported August 26, 2026 · Loaner insulin pumps may have been cleaned with chemically incompatible products that could damage the pump case or keypad, allow moisture ingress, and result... - MiniMed 670G Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported August 26, 2026 · Loaner insulin pumps may have been cleaned with chemically incompatible products that could damage the pump case or keypad, allow moisture ingress, and result... - MiniMed 640G Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported August 26, 2026 · Loaner insulin pumps may have been cleaned with chemically incompatible products that could damage the pump case or keypad, allow moisture ingress, and result... - BMC/REACTHEALTH Luna G3 APAP REF LG 3600 recall (BMC Medical Co., Ltd.)
Medical deviceClass IReported August 26, 2026 · Retroactive reporting for 2024 rework conducted at the 3B/React Health warehouse - Boston Scientific ENROUTE Transcarotid Neuroprotection System Plus recall (Boston Scientific Corporation)
Medical deviceClass IReported August 26, 2026 · Potential for arterial sheath tip separation or partial tip separation during use. - Boston Scientific ENROUTE Transcarotid Neuroprotection System recall (Boston Scientific Corporation)
Medical deviceClass IReported August 26, 2026 · Potential for arterial sheath tip separation or partial tip separation during use. - Beckman Coulter recall (Siemens Healthcare Diagnostics, Inc.)
Medical deviceClass IIReported August 26, 2026 · Due to unacceptable precision performance exhibited in certain lots of the Emit 2000 Quinidine Assay, which may lead to erroneously elevated quinidine... - Syva EMIT 2000 Quinidine Assay REF: 4Q019UL Contents: 1x28 mL recall (Siemens Healthcare Diagnostics, Inc.)
Medical deviceClass IIReported August 26, 2026 · Due to unacceptable precision performance exhibited in certain lots of the Emit 2000 Quinidine Assay, which may lead to erroneously elevated quinidine...