Recalls in March 2026 (page 4)

465 recalls.

• 5% Dextrose Injection recall (Fresenius Kabi USA, LLC)
  DrugClass IIReported April 15, 2026 · Lack of Assurance of Sterility
• 5% Dextrose Injection recall (Fresenius Kabi USA, LLC)
  DrugClass IIReported April 15, 2026 · Lack of Assurance of Sterility
• 5% Dextrose Injection recall (Fresenius Kabi USA, LLC)
  DrugClass IIReported April 15, 2026 · Lack of Assurance of Sterility
• 0.9% Sodium Chloride Injection recall (Fresenius Kabi USA, LLC)
  DrugClass IIReported April 15, 2026 · Lack of Assurance of Sterility
• 0.9% Sodium Chloride Injection recall (Fresenius Kabi USA, LLC)
  DrugClass IIReported April 15, 2026 · Lack of Assurance of Sterility
• 0.9% Sodium Chloride Injection recall (Fresenius Kabi USA, LLC)
  DrugClass IIReported April 15, 2026 · Lack of Assurance of Sterility
• 0.9% Sodium Chloride Injection recall (Fresenius Kabi USA, LLC)
  DrugClass IIReported April 15, 2026 · Lack of Assurance of Sterility
• 0.9% Sodium Chloride Injection recall (Fresenius Kabi USA, LLC)
  DrugClass IIReported April 15, 2026 · Lack of Assurance of Sterility
• 0.9% Sodium Chloride Injection recall (Fresenius Kabi USA, LLC)
  DrugClass IIReported April 15, 2026 · Lack of Assurance of Sterility
• 0.9% Sodium Chloride Injection recall (Fresenius Kabi USA, LLC)
  DrugClass IIReported April 15, 2026 · Lack of Assurance of Sterility
• 0.9% Sodium Chloride Injection recall (Fresenius Kabi USA, LLC)
  DrugClass IIReported April 15, 2026 · Lack of Assurance of Sterility
• 0.9% Sodium Chloride Injection recall (Fresenius Kabi USA, LLC)
  DrugClass IIReported April 15, 2026 · Lack of Assurance of Sterility
• 0.9% Sodium Chloride Injection recall (Fresenius Kabi USA, LLC)
  DrugClass IIReported April 15, 2026 · Lack of Assurance of Sterility
• 0.45% Sodium Chloride Injection recall (Fresenius Kabi USA, LLC)
  DrugClass IIReported April 15, 2026 · Lack of Assurance of Sterility
• Lanreotide Injection recall (Cipla USA, Inc.)
  DrugClass IIReported April 15, 2026 · Lack of Assurance of Sterility: Due to an FDA observation at the contract manufacturing site for deficiencies in their visual inspection procedure.
• Lanreotide Injection recall (Cipla USA, Inc.)
  DrugClass IIReported April 15, 2026 · Lack of Assurance of Sterility: Due to an FDA observation at the contract manufacturing site for deficiencies in their visual inspection procedure.
• Stryker Sustainability Solution Color Cuff 24" recall (Stryker Sustainability Solutions)
  Medical deviceClass IIReported April 15, 2026 · Due to potential for tourniquet cuffs to detach from the bladder at the welding connection and result in the cuff not being able to maintain pressure.
• B¿R¿A¿H¿M¿S KRYPTOR compact REACT recall (Brahms GmbH)
  Medical deviceClass IIReported April 15, 2026 · Customers have observed quality control values out of range at the lowest quality control level (QC Level 1) for the PIGF assay which require troubleshooting...
• COOK MEDICAL Wayne Pneumothorax Tray: Reference Part Number C-UTPTY-1400-WAYNE-112497-IMH recall (Cook Incorporated)
  Medical deviceClass IIReported April 15, 2026 · Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
• COOK MEDICAL Wayne Pneumothorax Set: Reference Part Number C-UTPT-1020-WAYNE-IMH recall (Cook Incorporated)
  Medical deviceClass IIReported April 15, 2026 · Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
• COOK MEDICAL Thal-Quick Chest Tube Tray: Reference Part Number C-TQTSY-3200 recall (Cook Incorporated)
  Medical deviceClass IIReported April 15, 2026 · Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
• COOK MEDICAL Spectrum¿ Central Venous Tray: Reference Part Number... recall (Cook Incorporated)
  Medical deviceClass IIReported April 15, 2026 · Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
• COOK MEDICAL Spectrum¿ Central Venous Catheter Set: Reference Part Number... recall (Cook Incorporated)
  Medical deviceClass IIReported April 15, 2026 · Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
• COOK MEDICAL NCompass¿ Nitinol Stone Extractor: Reference Part Number C-NTSE-2.4-115-NC3 recall (Cook Incorporated)
  Medical deviceClass IIReported April 15, 2026 · Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
• COOK MEDICAL Multipurpose Drainage Catheter: Reference Part Number... recall (Cook Incorporated)
  Medical deviceClass IIReported April 15, 2026 · Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
• Melker Universal Cuffed Emergency Cricothyrotomy Catheter Set: Reference Part Number... recall (Cook Incorporated)
  Medical deviceClass IIReported April 15, 2026 · Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
• COOK MEDICAL Cook¿ Strange Bile Duct Stone Exploration Set: Reference Part Number... recall (Cook Incorporated)
  Medical deviceClass IIReported April 15, 2026 · Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
• COOK MEDICAL Cook¿ Spectrum¿ Central Venous Catheter Tray: Reference Part Number... recall (Cook Incorporated)
  Medical deviceClass IIReported April 15, 2026 · Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
• COOK MEDICAL Cook Staged Extubation Set: Reference Part Number C-CAE-14.0-83-EXTU recall (Cook Incorporated)
  Medical deviceClass IIReported April 15, 2026 · Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
• COOK MEDICAL Ciaglia Blue Rhino Percutaneous Tracheostomy Introducer Set: Reference... recall (Cook Incorporated)
  Medical deviceClass IIReported April 15, 2026 · Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
• COOK MEDICAL Blue Rhino¿ G2-Multi Percutaneous Tracheostomy Introducer Tray: ... recall (Cook Incorporated)
  Medical deviceClass IIReported April 15, 2026 · Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
• COOK MEDICAL Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Set: Reference... recall (Cook Incorporated)
  Medical deviceClass IIReported April 15, 2026 · Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
• COOK MEDICAL Arterial Pressure Monitoring Tray recall (Cook Incorporated)
  Medical deviceClass IIReported April 15, 2026 · Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
• COOK MEDICAL Approach CTO-18 Micro Wire Guide recall (Cook Incorporated)
  Medical deviceClass IIReported April 15, 2026 · Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
• COOK MEDICAL Approach CTO-12 Micro Wire Guide: Reference Part Number CMW-14-190-12G recall (Cook Incorporated)
  Medical deviceClass IIReported April 15, 2026 · Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
• COOK MEDICAL Approach CTO-6 Micro Wire Guide recall (Cook Incorporated)
  Medical deviceClass IIReported April 15, 2026 · Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
• Tornier HRS Max parts: 1. TORNIER HRS Max Tuberosity Body Lat Coat recall (Tornier, Inc)
  Medical deviceClass IIReported April 15, 2026 · Affected products were incorrectly labeled as Tornier HRS Max products. These parts are compatible with the Tornier HRS system only, and are incompatible with...
• ARTIS pheno and ARTIS Icono biplane recall (Siemens Medical Solutions USA, Inc)
  Medical deviceClass IIReported April 15, 2026 · During patient examinations, the system may sporadically display a major increase of the x-ray dose applied to the patient. Despite the reported dose showing...
• Coconut Drink 1 recall (HEYTEA USA INC)
  FoodClass IIReported April 8, 2026 · Product contains undeclared milk.
• Spray Dried Dairy Powder 25 kg bags or 1 metric ton totes recall (Lone Star Dairy Products LLC)
  FoodClass IReported April 8, 2026 · Salmonella spp. identified in finished product testing
• " Dumpling Party Tray recall (JFE FRANCHISING INC)
  FoodClass IIReported April 8, 2026 · Foreign Object (Glass)
• " Dumpling Vegetable 4.5 oz ... recall (JFE FRANCHISING INC)
  FoodClass IIReported April 8, 2026 · Foreign Object (Glass)
• POPPING BOBA RTD MANGO PASSION FRUIT GREEN TEA 12 X 13.8OZ recall (Pocas International Corp.)
  FoodClass IIIReported April 8, 2026 · Packaging integrity issue that may compromise product quality .
• POPPING BOBA RTD STRAWBERRY DRAGON F/OOLONG TEA 12 X 13.8OZ recall (Pocas International Corp.)
  FoodClass IIIReported April 8, 2026 · Packaging integrity issue that may compromise product quality .
• POPPING BOBA RTD MIXED BERRY HIBISCUS TEA 12 X 13.8OZ recall (Pocas International Corp.)
  FoodClass IIIReported April 8, 2026 · Packaging integrity issue that may compromise product quality .
• POPPING BOBA RTD PEACH OOLONG TEA 12 X 13.8OZ recall (Pocas International Corp.)
  FoodClass IIIReported April 8, 2026 · Packaging integrity issue that may compromise product quality .
• Magnesium Sulfate in Water for Injection recall (Amneal Pharmaceuticals, LLC)
  DrugClass IReported April 8, 2026 · Product mix up: a foil pouch labeled "Magnesium Sulfate in Water for Injection, 4 g/100 mL" actually contained an IV bag of Tranexamic Acid instead.
• Prazosin Hydrochloride Capsules recall (Appco Pharma LLC)
  DrugClass IIReported April 8, 2026 · cGMP deviation: detection of Nitrosamine Drug Substance-Related Impurities, N-nitroso-prazosin impurity C (NNP) above acceptable limits.
• Prazosin Hydrochloride Capsules recall (Appco Pharma LLC)
  DrugClass IIReported April 8, 2026 · cGMP deviation: detection of Nitrosamine Drug Substance-Related Impurities, N-nitroso-prazosin impurity C (NNP) above acceptable limits.
• Prazosin Hydrochloride Capsules recall (Appco Pharma LLC)
  DrugClass IIReported April 8, 2026 · cGMP deviation: detection of Nitrosamine Drug Substance-Related Impurities, N-nitroso-prazosin impurity C (NNP) above acceptable limits.
• Artificial Tears Sterile Lubricant Eye Drops recall (K.C. Pharmaceuticals, Inc)
  DrugClass IIReported April 8, 2026 · Lack of Assurance of Sterility
• STERILE EYE DROPS SOOTHING TEARS recall (K.C. Pharmaceuticals, Inc)
  DrugClass IIReported April 8, 2026 · Lack of Assurance of Sterility
• Sterile EYE DROPS REDNESS LUBRICANT recall (K.C. Pharmaceuticals, Inc)
  DrugClass IIReported April 8, 2026 · Lack of Assurance of Sterility
• Sterile Eye Drops ORIGINAL FORMULA recall (K.C. Pharmaceuticals, Inc)
  DrugClass IIReported April 8, 2026 · Lack of Assurance of Sterility
• Ultra Lubricating Eye Drops recall (K.C. Pharmaceuticals, Inc)
  DrugClass IIReported April 8, 2026 · Lack of Assurance of Sterility
• Dry Eye Relief Eye Drops recall (K.C. Pharmaceuticals, Inc)
  DrugClass IIReported April 8, 2026 · Lack of Assurance of Sterility
• EYE DROPS Advanced Relief recall (K.C. Pharmaceuticals, Inc)
  DrugClass IIReported April 8, 2026 · Lack of Assurance of Sterility
• Sterile EYE DROPS AC recall (K.C. Pharmaceuticals, Inc)
  DrugClass IIReported April 8, 2026 · Lack of Assurance of Sterility
• traMADol Hydrochloride Tablets recall (Amneal Pharmaceuticals, LLC)
  DrugClass IIReported April 8, 2026 · Failed Impurities/Degradation Specifications: N-nitroso-desmethyl-tramadol impurity (NDSRI) was found out of the specification at 24-month stability interval...
• OXOID MICROBACT IDENTIFICATION KITS recall (Oxoid Australia Pty Limited)
  Medical deviceClass IIReported April 8, 2026 · Oxoid Ltd., part of Thermo Fisher Scientific, confirmed that Microbact 12L Kit 20 Tests MB1128A lot 4494873 may identify incorrect organism due to...
• eTRAX Needle Sensor - 18G recall (Civco Medical Instruments Co. Inc.)
  Medical deviceClass IIReported April 8, 2026 · There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be...
• eTRAX Needle Sensor - 16G recall (Civco Medical Instruments Co. Inc.)
  Medical deviceClass IIReported April 8, 2026 · There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be...
• eTRAX Needle Sensor - 14G recall (Civco Medical Instruments Co. Inc.)
  Medical deviceClass IIReported April 8, 2026 · There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be...
• eTRAX Needle Sensor - 12G recall (Civco Medical Instruments Co. Inc.)
  Medical deviceClass IIReported April 8, 2026 · There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be...
• eTRAX Needle System Starter Kit 18G recall (Civco Medical Instruments Co. Inc.)
  Medical deviceClass IIReported April 8, 2026 · There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be...
• eTRAX Needle System Starter Kit 16G recall (Civco Medical Instruments Co. Inc.)
  Medical deviceClass IIReported April 8, 2026 · There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be...
• eTRAX Needle System Starter Kit 14G recall (Civco Medical Instruments Co. Inc.)
  Medical deviceClass IIReported April 8, 2026 · There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be...
• eTRAX Needle System Starter Kit 12G recall (Civco Medical Instruments Co. Inc.)
  Medical deviceClass IIReported April 8, 2026 · There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be...
• Vue Motion V12. Product Number: 1017979. recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported April 8, 2026 · Potential that mis-ordered frames in Vue Motion during dynamic cine runs may cause images frames to display out of sequence.
• Azurion 5 M20 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
• Azurion 5 M12 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
• Azurion 7 M20 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
• Azurion 7 M12 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
• Azurion 7 B20 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
• Azurion 7 B12 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
• Azurion 3 M15 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
• Azurion 3 M12 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
• Allura Xper FD20/15 OR Table recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
• Allura Xper FD20/15 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
• Allura Xper FD20/20 OR Table recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
• Allura Xper FD20/20 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
• Allura Xper FD20/10 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
• ALLURA Xper FD10 OR Table recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
• ALLURA Xper FD20 Biplane OR Table recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
• ALLURA Xper FD20 OR Table recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
• ALLURA Xper FD20 Biplane recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
• ALLURA Xper FD20 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
• ALLURA Xper FD10/10 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
• ALLURA Xper FD10 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
• ALLURA Xper FD10F recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
• Allura Xper FD10C recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
• Philips Respironics Trilogy Evo Universal recall (Philips Respironics, Inc.)
  Medical deviceClass IReported April 8, 2026 · In some situations, the Obstruction Alarm does not trigger within the timeframe dictated by the relevant standards and may take up to four breaths.
• Philips Respironics Trilogy EV300 recall (Philips Respironics, Inc.)
  Medical deviceClass IReported April 8, 2026 · In some situations, the Obstruction Alarm does not trigger within the timeframe dictated by the relevant standards and may take up to four breaths.
• Philips Respironics Trilogy Evo O2 recall (Philips Respironics, Inc.)
  Medical deviceClass IReported April 8, 2026 · In some situations, the Obstruction Alarm does not trigger within the timeframe dictated by the relevant standards and may take up to four breaths.
• Philips Respironics Trilogy Evo recall (Philips Respironics, Inc.)
  Medical deviceClass IReported April 8, 2026 · In some situations, the Obstruction Alarm does not trigger within the timeframe dictated by the relevant standards and may take up to four breaths.
• Doraditas de Azucar recall (Distribuidora de Alimentos Sendero LLC)
  FoodClass IReported April 1, 2026 · Gorditas and Doraditas are missing the following allergens in product label: Wheat and Soy
• Gorditas de Azucar recall (Distribuidora de Alimentos Sendero LLC)
  FoodClass IReported April 1, 2026 · Gorditas and Doraditas are missing the following allergens in product label: Wheat and Soy
• Nuts.com recall (Nuts.com Inc.)
  FoodClass IReported April 1, 2026 · Undeclared Allergen - Wheat and Soy (from Soy Lecithin). The ingredient statement and allergen information do not include wheat or soy.
• Favorina Chocolate Ladybugs German-Style Nougat recall (Lidl US TRADING)
  FoodClass IIReported April 1, 2026 · Label does not specify type of tree nut contained in the product.
• Lucerne 2% Cottage Cheese 2% Milkfat Small Curd Vitamin A Added Grade A. Net wt.24oz.... recall (Albertsons Companies LLC)
  FoodClass IIReported April 1, 2026 · Metal fragments. The potential foreign object is a hard, metal (stainless steel), curled spring. Dimensions of a similar spring measure 2.27mm in...

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