Recalls in June 2026 (page 3)
405 recalls.
- MEDLINE ANTERIOR HIP recall (Medline Industries, LP)
Medical deviceClass IReported July 29, 2026 · Medline Industries, LP is issuing a recall for specific Medline kits containing B. Braun convenience kits that include Bupivacaine Hydrochloride in Dextrose... - OLA-OLA POUNDED GROUNDNUTS recall (Fayus Inc.)
FoodClass IIReported July 22, 2026 · Undeclared peanuts - Amy's ORGANIC SOUPS LENTIL LIGHT IN SODIUM recall (AMY'S KITCHEN INC.)
FoodClass IIReported July 22, 2026 · Potential for spoilage. - WY Duck Sauce recall (W.Y. Industries, Inc.)
FoodClass IIReported July 22, 2026 · Product may contain metal fragments. - Pillsbury Bread Rolls recall (General Mills James Ford Bell Technical Center)
FoodClass IIReported July 22, 2026 · Potential foreign material (glass) - Pillsbury Bread Rolls recall (General Mills James Ford Bell Technical Center)
FoodClass IIReported July 22, 2026 · Potential foreign material (glass) - 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... - The Vasoview Hemopro 2 Endoscopic Vessel Harvesting System recall (Maquet Cardiovascular, LLC)
Medical deviceClass IIReported July 22, 2026 · Getinge identified that Vasoview Hemopro 2 devices from Lot 3000547797 were exposed to an out-of-specification sterilization dose during a gamma sterilization... - Medline Kits containing Zimmer Biomet mixing bowls and spatulas TOTAL KNEE PACK-LF ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 22, 2026 · Kits contain Zimmer Biomet mixing bowls and spatulas, which were recalled due to seal nonconformities which present risk of sterility breach. Health... - Medline Kits containing Zimmer Biomet mixing bowls and spatulas TOTAL KNEE PACK ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 22, 2026 · Kits contain Zimmer Biomet mixing bowls and spatulas, which were recalled due to seal nonconformities which present risk of sterility breach. Health... - 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... - Optima XR240amx recall (GE Medical Systems, LLC)
Medical deviceClass IIReported July 22, 2026 · GE HealthCare has become aware that in certain Optima XR200/220/240amx systems that have had a column replacement completed, functional testing of the safety... - Optima XR220amx recall (GE Medical Systems, LLC)
Medical deviceClass IIReported July 22, 2026 · GE HealthCare has become aware that in certain Optima XR200/220/240amx systems that have had a column replacement completed, functional testing of the safety... - Optima XR200amx recall (GE Medical Systems, LLC)
Medical deviceClass IIReported July 22, 2026 · GE HealthCare has become aware that in certain Optima XR200/220/240amx systems that have had a column replacement completed, functional testing of the safety... - Rapid Refill Continuous Injection System recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 22, 2026 · Devices contain recalled Medline Namic Angiographic Control Syringe with Rotating Adaptor. There is a risk of syringe loosening or disconnecting from the... - ICU Medical Plum Solo Precision IV Pump recall (ICU Medical, Inc.)
Medical deviceClass IIReported July 22, 2026 · In a specific scenario, the pump will not decrement the Volume to be Infused (VTBI) displayed on the Delivery screen and may deliver up to twice the VTBI at... - ICU Medical Plum Duo Infusion Pump recall (ICU Medical, Inc.)
Medical deviceClass IIReported July 22, 2026 · In a specific scenario, the pump will not decrement the Volume to be Infused (VTBI) displayed on the Delivery screen and may deliver up to twice the VTBI at... - Bone Marrow Tray recall (Argon Medical Devices, Inc)
Medical deviceClass IReported July 22, 2026 · Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility. - Arterial Line Kit 20ga x 6 recall (Argon Medical Devices, Inc)
Medical deviceClass IReported July 22, 2026 · Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility. - T-Lok Bone Marrow Tray recall (Argon Medical Devices, Inc)
Medical deviceClass IReported July 22, 2026 · Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility. - General Biospy Tray recall (Argon Medical Devices, Inc)
Medical deviceClass IReported July 22, 2026 · Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility. - One-Piece Introducer Tray recall (Argon Medical Devices, Inc)
Medical deviceClass IReported July 22, 2026 · Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility. - Transvenous Pacing Electrode Tray w/ Bipolar Balloon Pacing Electrode 5F recall (Argon Medical Devices, Inc)
Medical deviceClass IReported July 22, 2026 · Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility. - 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... - Abiomed REF: 0052-3006 recall (Oscor Inc.)
Medical deviceClass IReported July 22, 2026 · Due to manufacturing issues, there is a potential for the 14Fr and 23Fr introducer sheaths to leak from the sidearm, under the sheath cap, and along the hub... - Abiomed REF: 0052-3021 recall (Oscor Inc.)
Medical deviceClass IReported July 22, 2026 · Due to manufacturing issues, there is a potential for the 14Fr and 23Fr introducer sheaths to leak from the sidearm, under the sheath cap, and along the hub... - Abiomed REF: 0052-3025 recall (Oscor Inc.)
Medical deviceClass IReported July 22, 2026 · Due to manufacturing issues, there is a potential for the 14Fr and 23Fr introducer sheaths to leak from the sidearm, under the sheath cap, and along the hub... - High Valley Orchard Chocolate Covered Raisins recall (Lehi Valley Trading Company, Inc)
FoodClass IReported July 15, 2026 · Undeclared Peanut. High Valley Orchard Chocolate Covered Raisins contains unintended undeclared peanut due to mis-packaging. - Fresh to You Burger Chicken Fillet recall (Fresh & Ready Foods LLC)
FoodClass IReported July 15, 2026 · Raw breaded chicken patties were inadvertently used in the ready to eat Burger Chicken Fillet sandwich. Raw breaded chicken patties pose a risk of foodborne... - Fresh to You Burger Chicken Fillet Deluxe with Bacon recall (Fresh & Ready Foods LLC)
FoodClass IReported July 15, 2026 · Raw breaded chicken patties were inadvertently used in the ready to eat Burger Chicken Deluxe With Bacon sandwich. Raw breaded chicken patties pose a risk of... - Alabama Banana Pudding Marshmallow recall (Wondermade LLC)
FoodClass IIReported July 15, 2026 · Foreign material: small metal pieces - Trafa Pharmaceuticals Inc. brand ORGANIC MORINGA LEAF POWDER recall (Trafa Pharmaceutical Inc.)
FoodClass IReported July 15, 2026 · Potential contamination with Salmonella - Bakr Brown Butter Chocolate Chunk Ready to Bake Cookie Dough recall (Bear Stewart Co)
FoodClass IIReported July 15, 2026 · undeclared soy - Johnny's Salad and Pasta Elegance 5.5 oz recall (Adams Extract & Spice LLC)
FoodClass IIReported July 15, 2026 · Undeclared Sesame allergen - Coopers Bbq 60 Gal Bean Mix box recall (Adams Extract & Spice LLC)
FoodClass IReported July 15, 2026 · Undeclared Sesame allergen - EC Hot Links Seasoning 45.05# recall (Adams Extract & Spice LLC)
FoodClass IReported July 15, 2026 · Undeclared Sesame allergen - JB Chicken Sknls 35.73# recall (Adams Extract & Spice LLC)
FoodClass IReported July 15, 2026 · Undeclared Sesame allergen - Smoked Sausage Spice 32.86# recall (Adams Extract & Spice LLC)
FoodClass IReported July 15, 2026 · Undeclared Sesame allergen - Azacitidine for Injection 100mg/Vial recall (Reliance Life Sciences Private Limited)
DrugClass IIReported July 15, 2026 · Lack of Sterility Assurance - Bortezomib for Injection 3.5mg/Vial recall (Reliance Life Sciences Private Limited)
DrugClass IIReported July 15, 2026 · Lack of Sterility Assurance - Pemetrexed for Injection 500mg/Vial recall (Reliance Life Sciences Private Limited)
DrugClass IIReported July 15, 2026 · Lack of Sterility Assurance - Pemetrexed for Injection 100mg/Vial recall (Reliance Life Sciences Private Limited)
DrugClass IIReported July 15, 2026 · Lack of Sterility Assurance - Methohexital Sodium recall (QuVa Pharma, Inc.)
DrugClass IIReported July 15, 2026 · Failed Impurities/Degradation Specifications - Medline Remedy Specialized Silicone Cream recall (BioMed Laboratories, LLC.)
DrugClass IIReported July 15, 2026 · Failed Impurities/Degradation Specifications; Formaldehyde levels exceeded specification. - Methohexital Sodium for Injection recall (ONESOURCE SPECIALTY PHARMA LIMITED)
DrugClass IIReported July 15, 2026 · Failed Impurities/Degradation Specifications - Brand Name: Versius Surgical System US Product Name: Vesius Surgeon Console US ... recall (CMR SURGICAL LIMITED)
Medical deviceClass IIReported July 15, 2026 · Secure Boot was mistakenly not enabled at manufacturing time, which presents a potential cybersecurity risk. - VITEK 2 AST-N447 TEST KIT Product reference 424620 recall (Biomerieux Inc)
Medical deviceClass IIReported July 15, 2026 · Potential for false resistant carbapenem and/or cephalosporin results when analyzing samples with kits from affected lot that have pouch foil fractures. - OmniTract Surgical Retractor System recall (Integra LifeSciences Corp. (NeuroSciences))
Medical deviceClass IIReported July 15, 2026 · The current Omni-Tract Surgical Retractor System IFU states a dry time of 30 minutes. Integra LifeSciences has identified that the dry time needs to be... - Atellica CH Enzymatic Hemoglobin A1c recall (Siemens Healthcare Diagnostics, Inc.)
Medical deviceClass IIReported July 15, 2026 · The potential for intermittent well-to-well bias on the A1c_E assay on the Atellica CH and Atellica CI analyzer which could cause falsely depressed or falsely... - KL Owen Custom Orthodontic Solution recall (Klowen Braces)
Medical deviceClass IIReported July 15, 2026 · A product error defect may cause incorrect bracket placement. - Aquacel Ag Surgical SP REF: 413556 9cm x 15cm/3.5 in. x 6 in. recall (ConvaTec, Inc)
Medical deviceClass IIReported July 15, 2026 · Surgical dressing manufactured out of specification (greater thickness). - Olympus Single Use Distal Cover recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported July 15, 2026 · Olympus has developed and released newly designed version of the Distal Cover (MAJ-2315) to replace previous design of the Single Use Distal Covers. - Plastic 1-gallon clear pail blue label which reads in part as "BLUE RIBBON CLASSICS... recall (Wells Enterprises, Inc.)
FoodClass IIReported July 8, 2026 · Elevated coliforms - a.) nara organics brand recall (NARA ORGANICS INC)
FoodClass IReported July 8, 2026 · Product may be contaminated with Clostridium botulinum. - Pepperoni Rolls recall (Fry Pie Factory LLC)
FoodClass IIReported July 8, 2026 · Undeclared allergen (milk) and process deviation (product not held under refrigeration as required) - Vista MAX recall (Provision Health Corp. dba PH Labs)
FoodClass IIReported July 8, 2026 · Dietary supplement product Vista MAX contains undeclared Yellow#5. - Ocular Plus with Lutein recall (Provision Health Corp. dba PH Labs)
FoodClass IIReported July 8, 2026 · Dietary supplement product Ocular Plus contains undeclared Yellow#5. - MorningStar Farms Hot & Spicy Sausage Patties recall (MARS SNACKING)
FoodClass IIReported July 8, 2026 · Potential contamination with plastic material - MorningStar Farms Buffalo Chik'n Nuggets recall (MARS SNACKING)
FoodClass IIReported July 8, 2026 · Potential contamination with plastic material - FIRST STREET Dark Chocolate Raisins Net Wt. 9 oz. recall (Western Mixers Produce & Nuts, Inc.)
FoodClass IReported July 8, 2026 · Undeclared peanuts. - Glucagon Emergency Kit for Low Blood Sugar recall (Lupin Pharmaceuticals Inc.)
DrugClass IIReported July 8, 2026 · CGMP deviation: OOS result observed for the Gliding Force functionality test during 12-month long term stability testing. - Gemcitabine Injection recall (McKesson)
DrugClass IIReported July 8, 2026 · Temperature Abuse: Product was stored incorrectly in a controlled room temperature environment instead of a refrigerated environment. - Cinacalcet Hydrochloride Tablets recall (Cipla USA, Inc.)
DrugClass IIReported July 8, 2026 · cGMP Deviations: presence of N-nitroso-cinacalcet, above the acceptable daily intake (ADI). - Cinacalcet Hydrochloride Tablets recall (Cipla USA, Inc.)
DrugClass IIReported July 8, 2026 · cGMP Deviations: presence of N-nitroso-cinacalcet, above the acceptable daily intake (ADI). - Cinacalcet Hydrochloride Tablets recall (Cipla USA, Inc.)
DrugClass IIReported July 8, 2026 · cGMP Deviations: presence of N-nitroso-cinacalcet, above the acceptable daily intake (ADI). - Dextroamphetamine Saccharate recall (Lannett Company Inc.)
DrugClass IIReported July 8, 2026 · Labeling: Label Mix-up: Capsules contain only immediate-release (IR) pellets while labeled as ER capsules. - Lidocaine HCl Injection USP recall (Asclemed USA Inc.)
DrugClass IIReported July 8, 2026 · Lack of Assurance of Sterility - Accucaine recall (Asclemed USA Inc.)
DrugClass IIReported July 8, 2026 · Lack of Assurance of Sterility - Synjardy XR Tablets recall (Boehringer Ingelheim Pharmaceuticals, Inc.)
DrugClass IIReported July 8, 2026 · CGMP Deviations: An incorrect detergent was used and the required swab sampling was not performed on a production hopper that had previously been used for a... - Levothyroxine Sodium Tablets recall (ACCORD HEALTHCARE, INC.)
DrugClass IIReported July 8, 2026 · Subpotent Drug - prednisoLONE Acetate Ophthalmic Suspension recall (Lupin Pharmaceuticals Inc.)
DrugClass IIReported July 8, 2026 · Presence of Foreign Substance - Fexofenadine Hydrochloride Tablets recall (SUN PHARMACEUTICAL INDUSTRIES INC)
DrugClass IIIReported July 8, 2026 · Failed Impurities/Degradation Specifications - IMULDOSA recall (ACCORD BIOPHARMA INC)
DrugClass IIReported July 8, 2026 · Lack of assurance of Sterility: