Recalls in Illinois (page 15)
4177 recalls.
- Divalproex Sodium Delayed-Release Tablets recall (Bionpharma Inc.)
DrugClass IIReported July 29, 2026 · Presence of Foreign Tablets/Capsules - Glycopyrrolate Oral Solution recall (Precision Dose Inc.)
DrugClass IIReported July 29, 2026 · Failed Impurities/Degradation Specifications - Dabigatran etexilate Capsules recall (Ascend Laboratories, LLC)
DrugClass IIIReported July 29, 2026 · Failed Impurities/Degradation Specifications: OOS result was observed during the related substance test analysis with respect to Impurity II, Impurity III and... - Dabigatran etexilate Capsules recall (Ascend Laboratories, LLC)
DrugClass IIIReported July 29, 2026 · Failed Impurities/Degradation Specifications: OOS result was observed during the related substance test analysis with respect to Impurity II, Impurity III and... - Cetirizine Hydrochloride Tablets USP 5 mg recall (JB Chemicals and Pharmaceuticals Ltd)
DrugClass IReported July 29, 2026 · Cross Contamination with Other Products: Customer complaints for appearance of discolored tablets and red dots observed on Cetirizine Hydrochloride Tablets... - Xylocaine recall (Fresenius Kabi USA, LLC)
DrugClass IIReported July 29, 2026 · Presence of Particulate Matter: Hair was found in products - Xylocaine recall (Fresenius Kabi USA, LLC)
DrugClass IIReported July 29, 2026 · Presence of Particulate Matter: Hair was found in products - Naropin recall (Fresenius Kabi USA, LLC)
DrugClass IIReported July 29, 2026 · Presence of Particulate Matter: Hair was found in products - Lidocaine HCl Injection recall (Fresenius Kabi USA, LLC)
DrugClass IIReported July 29, 2026 · Presence of Particulate Matter: Hair was found in products - Glycopyrrolate Injection recall (Fresenius Kabi USA, LLC)
DrugClass IIReported July 29, 2026 · Presence of Particulate Matter: Hair was found in product - Rising recall (Rising Pharma Holding, Inc.)
DrugClass IIReported July 29, 2026 · Presence of Precipitate: medication was crystallizing and particles floating in the bottle - Rohto Cooling Eye Drops Cool Relief recall (Rohto-Mentholatum (Vietnam) Co., Ltd.)
DrugClass IIReported July 29, 2026 · Lack of Assurance of Sterility - Rohto Cooling Eye Drops Dry Aid recall (Rohto-Mentholatum (Vietnam) Co., Ltd.)
DrugClass IIReported July 29, 2026 · Lack of Assurance of Sterility - Rohto Cooling Eye Drops Dry Aid recall (Rohto-Mentholatum (Vietnam) Co., Ltd.)
DrugClass IIReported July 29, 2026 · Lack of Assurance of Sterility - Rohto Cooling Eye Drops Digi Eye recall (Rohto-Mentholatum (Vietnam) Co., Ltd.)
DrugClass IIReported July 29, 2026 · Lack of Assurance of Sterility - Rohto Cooling Eye Drops Optic Glow recall (Rohto-Mentholatum (Vietnam) Co., Ltd.)
DrugClass IIReported July 29, 2026 · Lack of Assurance of Sterility - Rohto Cooling Eye Drops Max Strength recall (Rohto-Mentholatum (Vietnam) Co., Ltd.)
DrugClass IIReported July 29, 2026 · Lack of Assurance of Sterility - Rohto Cooling Eye Drops Max Strength recall (Rohto-Mentholatum (Vietnam) Co., Ltd.)
DrugClass IIReported July 29, 2026 · Lack of Assurance of Sterility - Rohto Cooling Eye Drops ALL-IN-ONE recall (Rohto-Mentholatum (Vietnam) Co., Ltd.)
DrugClass IIReported July 29, 2026 · Lack of Assurance of Sterility - Amlodipine and Olmesartan Medoxomil Tablets recall (Ascend Laboratories, LLC)
DrugClass IIReported July 29, 2026 · Failed Dissolution Specifications; Olmesartan Medoxomil content below specifications - Levothyroxine Sodium Tablets recall (Major Pharmaceuticals)
DrugClass IIReported July 29, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (Major Pharmaceuticals)
DrugClass IIReported July 29, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (Major Pharmaceuticals)
DrugClass IIReported July 29, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (Major Pharmaceuticals)
DrugClass IIReported July 29, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (Major Pharmaceuticals)
DrugClass IIReported July 29, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (Major Pharmaceuticals)
DrugClass IIReported July 29, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (Major Pharmaceuticals)
DrugClass IIReported July 29, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (Major Pharmaceuticals)
DrugClass IIReported July 29, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (Major Pharmaceuticals)
DrugClass IIReported July 29, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (Major Pharmaceuticals)
DrugClass IIReported July 29, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (Major Pharmaceuticals)
DrugClass IIReported July 29, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (Major Pharmaceuticals)
DrugClass IIReported July 29, 2026 · Subpotent Drug - Flexible Hystero-Fiberscope Kits REF: 11264BBU1 recall (Karl Storz Endoscopy)
Medical deviceClass IIReported July 29, 2026 · Flexible hysteroscopes indicated for use during diagnostic and operative hysteroscopic procedures may contain an expired single use endoscopic seal for... - SafeOp Patient Interface recall (Alphatec Spine, Inc.)
Medical deviceClass IIReported July 29, 2026 · Intraoperative neuromonitoring device, due to a software issue, may experience loss or interruption of triggered electromyography (tEMG) functionality during... - Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters recall (Medline Industries, LP)
Medical deviceClass IIReported July 29, 2026 · Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the... - Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters recall (Medline Industries, LP)
Medical deviceClass IIReported July 29, 2026 · Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the... - Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters recall (Medline Industries, LP)
Medical deviceClass IIReported July 29, 2026 · Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the... - Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters recall (Medline Industries, LP)
Medical deviceClass IIReported July 29, 2026 · Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the... - Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters recall (Medline Industries, LP)
Medical deviceClass IIReported July 29, 2026 · Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the... - Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters recall (Medline Industries, LP)
Medical deviceClass IIReported July 29, 2026 · Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the... - Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters recall (Medline Industries, LP)
Medical deviceClass IIReported July 29, 2026 · Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the... - Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters recall (Medline Industries, LP)
Medical deviceClass IIReported July 29, 2026 · Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the... - Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters recall (Medline Industries, LP)
Medical deviceClass IIReported July 29, 2026 · Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the... - Emano Flow with software version v2.0.0 GS1 GTIN code: 199874903484 Emano Flow is... recall (Emano Metrics, Inc.)
Medical deviceClass IIReported July 29, 2026 · Problem description/Reason for recall: During the period March 22, 2026, to May 29, 2026, recorded urination audio was captured at 48,000 Hz while the model... - Olympus High Flow Insufflation Unit - UHI-4. Model Number: UHI-4 recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported July 29, 2026 · Potential for unexpected instances where the front panel display turns off unexpectedly, and air delivery (insufflation) ceases. - Pipeline Flex Embolization Device with Shield Technology recall (Micro Therapeutics, Inc.)
Medical deviceClass IIReported July 29, 2026 · Incorrect labeling - embolization devices labeled as 3.0 mm x 20 mm implants contain 12 mm implants, and devices labeled as 3.0 mm x 12 mm implants contain 20... - Pipeline Flex Embolization Device with Shield Technology recall (Micro Therapeutics, Inc.)
Medical deviceClass IIReported July 29, 2026 · Incorrect labeling - embolization devices labeled as 3.0 mm x 20 mm implants contain 12 mm implants, and devices labeled as 3.0 mm x 12 mm implants contain 20... - Halyard STANDARD LINE INSERTION PACK. Model/Catalog Number: PVHM234-01. ... recall (AVID Medical, Inc.)
Medical deviceClass IIReported July 29, 2026 · Defects in the silicone seal, which may result in "doming" of the silicone seal due to improper sealing, potentially leading to fluid occlusion or leakage. - 3mensio Workstation recall (PIE Medical Imaging B.V.)
Medical deviceClass IIReported July 29, 2026 · User measurement value reported by diagnostic bioimaging software intended to measure/visualize cardiovascular structures may be larger (0.8% to 34.4%) than... - Halyard EYE PACK. Model/Catalog Number: LVEY27 Convenience kit. recall (AVID Medical, Inc.)
Medical deviceClass IIReported July 29, 2026 · Incorrect concentration of Betadine solution contained within certain AVID convenience kits. - Olympus 4K UHD LCD Monitor. Model Number: OEV321UH. An electrically powered visual... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported July 29, 2026 · Potential for the HDMI and DisplayPort (DP) connectors can become faulty resulting in image loss or image abnormalities. - Hotline Fluid Warming Set recall (ICU Medical Inc.)
Medical deviceClass IIReported July 29, 2026 · ICU Medical became aware of an increased likelihood of leakage in specific Lots of L-70 HOTLINE Fluid Warming Sets due to potentially inadequate solvent... - P28 PHANTON INTRAMEDULLARY NAIL SYSTEM recall (Paragon 28, Inc.)
Medical deviceClass IIReported July 29, 2026 · Paragon 28 received two (2) complaints were received involving breaches in the sterile barrier of the pouch packaging. - FARADRIVE STEERABLE SHEATH CLEAR OUS recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 29, 2026 · Boston Scientific's complaint investigations have identified that a subset of air ingress complaints are associated with hemostatic valve damage related to... - FARADRIVE STEERABLE SHEATH recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 29, 2026 · Boston Scientific's complaint investigations have identified that a subset of air ingress complaints are associated with hemostatic valve damage related to... - FARADRIVE STEERABLE SHEATH CLEAR recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 29, 2026 · Boston Scientific's complaint investigations have identified that a subset of air ingress complaints are associated with hemostatic valve damage related to... - FARADRIVE Steerable Sheath Clear IDE recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 29, 2026 · Boston Scientific's complaint investigations have identified that a subset of air ingress complaints are associated with hemostatic valve damage related to... - The intended use is to be paired with a weapon for aiming purposes. recall (Wilcox Industries Corp.)
Medical deviceClass IIReported July 29, 2026 · Wilcox is notifying all customers who have purchased a product from the BOSS Xe family that a software enhancement to increase safety has been released and all... - Peony Design Recalls Personalized Baby Bibs and Stroller Bags Due to Risk of Serious Injury or Death from Choking Hazard
Consumer productReported July 24, 2026 · The snap can detach from the recalled bibs and stroller bags, posing a risk of serious injury or death from a choking hazard to young children. - CuddleCubs Creations Teething Toy Sets Recalled Due to Risk of Serious Injury or Death from Choking; Violate Mandatory Standard for Toys; Sold on Amazon by YouRfocus
Consumer productReported July 24, 2026 · The recalled teething toy sets contain a pull string teething toy that violates the mandatory standard for toys because the silicone strings are smaller and... - OeyUoc Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violate Virginia Graeme Baker Pool & Spa Safety Act; Sold Exclusively on Amazon by Yuanxinxiang
Consumer productReported July 24, 2026 · The recalled drain covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing deadly entrapment and... - Sviyatp Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violate Virginia Graeme Baker Pool & Spa Safety Act
Consumer productReported July 24, 2026 · The recalled drain covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing deadly entrapment and... - Aojieni Silicone Recalls Sili Factory Pull String Teething Toys Due to Risk of Serious Injury or Death from Choking; Violate Mandatory Standard for Toys
Consumer productReported July 24, 2026 · The recalled teething toys violate the mandatory standard for toys because the silicone strings are smaller and longer than permitted. The strings can reach... - 12-Drawer Fabric Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violate Mandatory Standard for Clothing Storage Units; Sold on Amazon by Romorgniz
Consumer productReported July 24, 2026 · The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or... - EnHomee 9-Drawer Fabric Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violates Mandatory Standard for Clothing Storage Units; Sold on Walmart.com by Raybee-Direct
Consumer productReported July 24, 2026 · The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risk of serious injuries or... - Amy's ORGANIC SOUPS LENTIL LIGHT IN SODIUM recall (AMY'S KITCHEN INC.)
FoodClass IIReported July 22, 2026 · Potential for spoilage. - functional formularies NOURISH ORGANIC WHOLE FOODS MEAL REPLACEMENT PEPTIDE FORMULA... recall (Nutricia North America)
FoodClass IIReported July 22, 2026 · Subpotent for Vitamin A. The firm discovered that the testing laboratory used the wrong method when testing for Vitamin A. The test results gave a higher... - functional formularies LIQUID HOPE ORGANIC WHOLE FOODS MEAL REPLACEMENT PEPTIDE... recall (Nutricia North America)
FoodClass IIReported July 22, 2026 · Subpotent for Vitamin A. The firm discovered that the testing laboratory used the wrong method when testing for Vitamin A. The test results gave a higher... - Orthofix MINIRAIL recall (Orthofix U.S. LLC)
Medical deviceClass IIReported July 22, 2026 · Unilateral external fixation devices may be incorrectly labeled. Minirail M101 was labeled as M103, Minirail M103 was labeled as M101, and Minirail M122 was... - Orthofix ARTICULATED MINIRAIL FIXATOR HORIZONTAL AXIS REF: M111 recall (Orthofix U.S. LLC)
Medical deviceClass IIReported July 22, 2026 · Unilateral external fixation devices may be incorrectly labeled. Minirail M101 was labeled as M103, Minirail M103 was labeled as M101, and Minirail M122 was... - Orthofix MINIRAIL recall (Orthofix U.S. LLC)
Medical deviceClass IIReported July 22, 2026 · Unilateral external fixation devices may be incorrectly labeled. Minirail M101 was labeled as M103, Minirail M103 was labeled as M101, and Minirail M122 was... - Orthofix MINIRAIL recall (Orthofix U.S. LLC)
Medical deviceClass IIReported July 22, 2026 · Unilateral external fixation devices may be incorrectly labeled. Minirail M101 was labeled as M103, Minirail M103 was labeled as M101, and Minirail M122 was... - ABIOMED Intro Kit recall (Abiomed, Inc.)
Medical deviceClass IReported July 22, 2026 · A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing... - ABIOMED Insertion Kit recall (Abiomed, Inc.)
Medical deviceClass IReported July 22, 2026 · A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing... - ABIOMED Impella CP Set recall (Abiomed, Inc.)
Medical deviceClass IReported July 22, 2026 · A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing... - ABIOMED Impella CP Smart Assist Set recall (Abiomed, Inc.)
Medical deviceClass IReported July 22, 2026 · A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing... - ABIOMED Impella CP Set recall (Abiomed, Inc.)
Medical deviceClass IReported July 22, 2026 · A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing... - ABIOMED Impella 5.5 SmartAssist S2 Set recall (Abiomed, Inc.)
Medical deviceClass IReported July 22, 2026 · A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing... - ABIOMED Impella 5.5 Smart Assist Set recall (Abiomed, Inc.)
Medical deviceClass IReported July 22, 2026 · A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing... - ABIOMED Impella CP Introducer Kit 14 Fr recall (Abiomed, Inc.)
Medical deviceClass IReported July 22, 2026 · A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing... - ABIOMED Impella CP Introducer Kit 14 Fr recall (Abiomed, Inc.)
Medical deviceClass IReported July 22, 2026 · A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing... - ABIOMED Introducer Kit 23 Fr recall (Abiomed, Inc.)
Medical deviceClass IReported July 22, 2026 · A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing... - ABIOMED Impella CP Introducer Kit 14 Fr recall (Abiomed, Inc.)
Medical deviceClass IReported July 22, 2026 · A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing... - ABIOMED Impella CP Set recall (Abiomed, Inc.)
Medical deviceClass IReported July 22, 2026 · A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing... - ABIOMED Impella RP Flex with SmartAssist Set recall (Abiomed, Inc.)
Medical deviceClass IReported July 22, 2026 · A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing... - BD ChloraPrep Clear recall (CareFusion 213, LLC)
DrugClass IIReported July 22, 2026 · Lack of Assurance of Sterility: Affected product may exhibit an open or incomplete seal on the packaging of the applicator - CLEVIPREX recall (Chiesi USA, Inc.)
DrugClass IIReported July 22, 2026 · Lack of Assurance of Sterility - CAREone recall (Bell Pharmaceuticals, Inc)
DrugClass IIReported July 22, 2026 · SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%). - meijer recall (Bell Pharmaceuticals, Inc)
DrugClass IIReported July 22, 2026 · SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%). - Foster & Thrive recall (Bell Pharmaceuticals, Inc)
DrugClass IIReported July 22, 2026 · SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%). - LEADER recall (Bell Pharmaceuticals, Inc)
DrugClass IIReported July 22, 2026 · SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%). - GOOD NEIGHBOR PHARMACY recall (Bell Pharmaceuticals, Inc)
DrugClass IIReported July 22, 2026 · SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%). - FAMILY Wellness recall (Bell Pharmaceuticals, Inc)
DrugClass IIReported July 22, 2026 · SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%). - AUDIOLOGIST'S CHOICE recall (Bell Pharmaceuticals, Inc)
DrugClass IIReported July 22, 2026 · SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%). - TopCare Health recall (Bell Pharmaceuticals, Inc)
DrugClass IIReported July 22, 2026 · SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%). - QC Quality Choice recall (Bell Pharmaceuticals, Inc)
DrugClass IIReported July 22, 2026 · SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%). - Clinere recall (Bell Pharmaceuticals, Inc)
DrugClass IIReported July 22, 2026 · SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%). - CVS Health recall (Bell Pharmaceuticals, Inc)
DrugClass IIReported July 22, 2026 · SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%). - Nystatin Cream USP recall (Padagis US LLC)
DrugClass IIReported July 22, 2026 · Subpotent Drug: Low out of specification assay results performed during long-term stability testing. - ST AIA-Pack Testosterone recall (Tosoh Bioscience Inc)
Medical deviceClass IIReported July 22, 2026 · The Test cup lot F level 1 low-quality control results values for the device were lower than expected on the Automated Immunoassay Analyzer (AIA) which could...