Recalls in California (page 4)
4209 recalls.
- LeadCare II Blood Lead Test Kit. Model/Catalog Number: 70-6762. recall (Magellan Diagnostics, Inc.)
Medical deviceClass IIIReported October 21, 2026 · In kit sub-lot 2530M-01 the date of expiration printed on the outer labeling may indicate the wrong expiration date of July 22, 2026 while the correct... - IQ200 SPRINT recall (Beckman Coulter, Inc.)
Medical deviceClass IIReported October 21, 2026 · The rinse-line check valve has a shorter service lifespan than originally expected and requires annual replacement to prevent lamina fluid leakage; however... - DxU 840m Iris recall (Beckman Coulter, Inc.)
Medical deviceClass IIReported October 21, 2026 · The rinse-line check valve has a shorter service lifespan than originally expected and requires annual replacement to prevent lamina fluid leakage; however... - MAS Omni IMMUNE PRO Liquid Assayed Integrated Immunoassay Control recall (Microgenics Corporation)
Medical deviceClass IIReported October 21, 2026 · Vial-to-vial variability in MAS¿ Omni"IMMUNE PRO Liquid Assayed Integrated Immunoassay Control, Level 1, Lot OPRO29061A results in low Parathyroid Hormone... - PERMA-HAND Silk Black Braided Sterile Nonabsorbable Surgical Suture recall (Ethicon, LLC)
Medical deviceClass IIReported October 21, 2026 · Silk sutures, indicated for use in cardiovascular, ophthalmic and neurological procedures, packaged with alcohol-based fluid, not part of product design, that... - Likorall Overhead Lifts Product Code: 3121001 Product Description: LIKORALL 200 ... recall (Baxter Healthcare Corporation)
Medical deviceClass IIReported October 21, 2026 · Potential issue involving motor shaft breakage combined with reduced performance of the Single Fault Safety (SFS) system may lead to instances where the lift... - Generic Name: BioFire¿ Joint Infection recall (BioFire Diagnostics, LLC)
Medical deviceClass IIReported October 21, 2026 · Due to potential contaiminated of spefic lots of pneumonia and joint infection panels that could result in false positive results - Generic Name: FilmArray¿ Pneumonia Panel plus Generic Name: FilmArray¿ Pneumonia Panel... recall (BioFire Diagnostics, LLC)
Medical deviceClass IIReported October 21, 2026 · Due to potential contaiminated of spefic lots of pneumonia and joint infection panels that could result in false positive results - Generic Name: FilmArray¿ Pneumonia Panel Generic Name: FilmArray¿ Pneumonia Panel ... recall (BioFire Diagnostics, LLC)
Medical deviceClass IIReported October 21, 2026 · Due to potential contaiminated of spefic lots of pneumonia and joint infection panels that could result in false positive results - Power F2 Powered Fastening System recall (Ferno-Washington Inc)
Medical deviceClass IIReported October 21, 2026 · Firmware issue may result in intermittent loss or degradation of powered functionality when paired with compatible stretcher. The issue may lead to the system... - NaviFlex LW Pusher recall (Boston Scientific Corporation)
Medical deviceClass IIReported October 21, 2026 · Device was incorrectly manufactured with a guidewire exit port (referred to in the IFU as the RX port), which is not a design feature associated with this... - JenaValve Trilogy Delivery Catheter recall (Jenavalve Technology Inc.)
Medical deviceClass IIReported October 21, 2026 · Delivery Catheter may have sleeve liner separation that results in difficulty or inability to deploy heart valve device. - JenaValve Trilogy Delivery Catheter recall (Jenavalve Technology Inc.)
Medical deviceClass IIReported October 21, 2026 · Delivery Catheter may have sleeve liner separation that results in difficulty or inability to deploy heart valve device. - JenaValve Trilogy Delivery Catheter recall (Jenavalve Technology Inc.)
Medical deviceClass IIReported October 21, 2026 · Delivery Catheter may have sleeve liner separation that results in difficulty or inability to deploy heart valve device. - HemoslL AcuStar HIT-lgG recall (Instrumentation Laboratory)
Medical deviceClass IReported October 21, 2026 · Potential for invalid calibration curve or negative mean bias of up to 47% with patient samples. - HemoslL AcuStar HIT-lgG recall (Instrumentation Laboratory)
Medical deviceClass IReported October 21, 2026 · Potential for invalid calibration curve or negative mean bias of up to 47% with patient samples. - Metoclopramide Tablets recall (American Health Packaging)
DrugClass IIReported October 21, 2026 · Presence of Foreign Tablets/Capsules - Sermorelin recall (Houston Rx LLC)
DrugClass IIReported October 21, 2026 · Lack of process control - Tirzepatide/Niacinamide 2mL vial recall (Houston Rx LLC)
DrugClass IIReported October 21, 2026 · Lack of assurance of sterility. - Hydrocortisone Sodium Succinate for Injection recall (Zydus Pharmaceuticals (USA) Inc)
DrugClass IIReported October 21, 2026 · Failed Impurities/Degradation Specifications. - Metoclopramide Tablets recall (Teva Pharmaceuticals USA, Inc)
DrugClass IIReported October 21, 2026 · Presence of Foreign Tablets/Capsules - Medline convenience kit labeled as: FOOT ANKLE. Medline Kit SKU DYNJ65395A recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Discrepancy in the shelf-life of a component - Vinyl Instrument Guards recall (Healthmark Industries Co., Inc.)
Medical deviceClass IIReported October 21, 2026 · Labeling not compliant with 21 CFR 801 and steam sterilization IFU has been updated. - IntelePACS recall (INTELERAD MEDICAL SYSTEMS INCORPORATED)
Medical deviceClass IIReported October 21, 2026 · Following a Chromium-based web-browser, report and displayed images may not match. - Medline surgical convenience kits labeled as: 1) SPINAL CDS recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to... - Medline surgical convenience kits labeled as: OPEN HEART recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to... - Medline surgical convenience kits labeled as: 1) NEURO-SPINE BASIN PACK recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to... - Medline surgical convenience kits labeled as: 1) OPEN HEART PACK A & recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to... - Medline surgical convenience kits labeled as: 1) CV BASIN PACK-LF recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to... - Medline surgical convenience kits labeled as: 1) MAIN/LAPAROSCOPY TRANSPLA PACK recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to... - Medline surgical convenience kits labeled as: 1) EAR recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to... - Medline surgical convenience kits labeled as: VEIN HARVESTING PACK recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to... - Medline surgical convenience kits labeled as: 1) VEIN HARVESTING PACK-LF recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to... - Medline surgical convenience kits labeled as: 1) OPEN HEART CDS recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to... - 1) Product Name AUD OPEN HEART PACK recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to... - Medline surgical convenience kits labeled as: CABG AUXILIARY PACK recall (Medline Industries, LP)
Medical deviceClass IIReported October 21, 2026 · Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to... - Generic Name: GORE VIABIL Short Wire Biliary Endoprosthesis recall (W L Gore & Associates, Inc.)
Medical deviceClass IIReported October 21, 2026 · The potential for the devices to be mislabeled with the incorrect length. - REF: P65 ST862 CoLag SCREW recall (In2bones USA, LLC)
Medical deviceClass IIReported October 21, 2026 · Due to labeling error, bone screws specified as fully threaded, are actually partially threaded screws. - RAPICIDE PA Part A High-Level Disinfectant recall (Steris Corporation)
Medical deviceClass IIReported October 21, 2026 · If the vented cap becomes blocked, gas may accumulate and the bottle may swell due to increased internal pressure. In some cases, excess vapor or liquid... - RAPICIDE PA Part A High-Level Disinfectant recall (Steris Corporation)
Medical deviceClass IIReported October 21, 2026 · If the vented cap becomes blocked, gas may accumulate and the bottle may swell due to increased internal pressure. In some cases, excess vapor or liquid... - RAPICIDE PA Part A High-Level Disinfectant recall (Steris Corporation)
Medical deviceClass IIReported October 21, 2026 · If the vented cap becomes blocked, gas may accumulate and the bottle may swell due to increased internal pressure. In some cases, excess vapor or liquid... - FORWARD Gunshot Wound Kit recall (INTEGRATED MEDCRAFT LLC)
Medical deviceClass IIReported October 21, 2026 · Subrecall of a kitted device from SafeGuard Medical due to internal testing identified an issue affecting the device's sterile pad, potentially causing the... - iFuse TORQ Implant System Model/Catalog Number: 10055T recall (SI-BONE, Inc.)
Medical deviceClass IIReported October 21, 2026 · The pelvic fixation screws failed to meet acceptance criteria for tube packaging seal integrity testing; therefore, sterility assurance cannot be ensured. - Curaplex Capnography EtCO2/O2 Oral/Nasal Cannula Multipack recall (Sarnova HC, Llc)
Medical deviceClass IIReported October 21, 2026 · Affected kits were assembled with pediatric nasal cannula instead of the intended adult nasal cannula. - NeuroStar Advanced Therapy System. Contains the NeuroStar HP Coil Assembly Part Number... recall (Neuronetics, Inc.)
Medical deviceClass IIReported October 21, 2026 · Cables are not in conformance with the product specifications required in the production of the HP Coil Assembly. - Brand Name: IOMAX Product Name: IOMAX Cortical Module Model/Catalog Number:... recall (Cadwell Industries Inc)
Medical deviceClass IIReported October 21, 2026 · Stimulator device contains a defective printed circuit board assembly (PCBA) that may cause the device to unintentionally deliver electrical stimulation to the... - BD Phoenix Panel NMIC-306. Catalog Number: 449292. recall (Becton Dickinson & Co.)
Medical deviceClass IIReported October 21, 2026 · Potential for quality control failures with Klebsiella pneumoniae ATCC BAA-1705 when using the CPO Ambler classification feature. - BD Phoenix Panel NMIC-312. Catalog Number: 449082. recall (Becton Dickinson & Co.)
Medical deviceClass IIReported October 21, 2026 · Potential for quality control failures with Klebsiella pneumoniae ATCC BAA-1705 when using the CPO Ambler classification feature. - Grafton" DBM and Grafton Plus" DBM contain demineralized human bone tissue combined... recall (Medtronic Sofamor Danek USA Inc)
Medical deviceClass IIReported October 21, 2026 · Medtronic identified through donor record review that the donor for Medtronic batch A62881 did not meet all Medtronic donor eligibility requirements related to... - Grafton" DBM and Grafton Plus" DBM contain demineralized human bone tissue combined... recall (Medtronic Sofamor Danek USA Inc)
Medical deviceClass IIReported October 21, 2026 · Medtronic identified through donor record review that the donor for Medtronic batch A62881 did not meet all Medtronic donor eligibility requirements related... - usOpal Recalls Xalirium Portable Bed Rails Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violate Mandatory Standard for Adult Portable Bed Rails
Consumer productReported October 15, 2026 · The recalled bed rails violate the mandatory standard for adult portable bed rails because when the bed rails are attached to a bed, users can become entrapped... - Primark Recalls 101 Dalmatians Faux Leather Children’s Coin Purses Due to Phthalate Levels and Risk of Ingestion
Consumer productReported October 15, 2026 · The coin purses contain higher phthalate concentration levels. Phthalates can be harmful if young children are exposed to sufficient amounts, including through... - Papablic, of USA Recalls Convertible Bedside Sleepers Due to Risk of Serious Injury or Death from Entrapment, Suffocation and Fall Hazards; Violate Mandatory Standard for Play Yards
Consumer productReported October 15, 2026 · The bedside sleepers with play yard extensions violate the mandatory safety standard for play yards because the mattress can become displaced, causing a baby... - Loving Thyself Rocks Recalls Crystal Glass Cups Due to Risk of Serious Injury from Ingestion and Laceration Hazards
Consumer productReported October 15, 2026 · Glass can break inside the recalled cups while in use, posing a risk of serious injury from ingestion and laceration hazards. - HatsanUSA Recalls Blitz Air Rifles Due to Risk of Serious Injury or Death from Projectile Hazard
Consumer productReported October 15, 2026 · The recalled air rifles can fire unexpectedly when releasing the bolt before the air rifle is fully cocked, posing a risk of serious injury or death from... - 3M Company Recalls Scotch™ Thermal Laminators Due to Risk of Serious Injury or Death from Fire Hazard
Consumer productReported October 15, 2026 · The recalled thermal laminators can overheat, posing a fire hazard. - SIERRA NEVADA CHEESE GRAZIERS RAW MILK SHARP CHEDDAR recall (Sierra Nevada Cheese Company, Inc)
FoodNot Yet ClassifiedReported October 14, 2026 · Potential contamination due to E. coli O26:H11. - 28 oz. Gatorade Lemon Lime recall (Pepsico Inc)
FoodClass IIReported October 14, 2026 · Undeclared Yellow No. 6 and/or Yellow No. 5 - WinCo Foods Salsa Bean Dip Express Tray is packaged in a foil bottom container with... recall (WinCo Foods LLC)
FoodClass IIReported October 14, 2026 · Bean Dip Trays contains recalled Peperoncini (pepper) which was recalled due to pest issue. - Mezzetta GOLDEN GREEK PEPERONCINI MEDIUM HEAT 32 FL OZ G.L. MEZZETTA recall (G L Mezzetta Inc)
FoodClass IIReported October 14, 2026 · Potential contamination with foreign objects: mice. - Biospectra Tris/Tromethamine recall (BioSpectra, Inc.)
DrugClass IIReported October 14, 2026 · Failed stability specifications - Intellijoint Navigation System: Workstation G2 Configured recall (Intellijoint Surgical, Inc.)
Medical deviceClass IIReported October 14, 2026 · A navigation system used to aid in selection and positioning of orthopedic implant system components has a workstation that may contain a 15-inch MacBook Pro... - TufTex¿ Over-the-Wire Embolectomy Catheter recall (LeMaitre Vascular, Inc.)
Medical deviceClass IIReported October 14, 2026 · Devices failed in process testing related to the amount of pull force it can sustain prior to the balloon components failing. - SEDIPLAST recall (POLYMEDCO, INC. / POLYMEDCO CANCER DIAGNOSTIC PRODUCTS, LLC)
Medical deviceClass IIReported October 14, 2026 · During use of an affected tube, the operator may encounter increased resistance when inserting the pipette. The resulting pressure buildup may cause the tube... - ABD HYSTERECTOMY recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - GYN LAPAROSCOPY PACK recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - MAJOR PACK recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - UROLOGY MAJOR recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - HEART PREP TRAY recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - DAVINCI LAP/GYN recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - PLASTICS TRAY recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - LAPAROSCOPIC PROSTATECTOMY recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - ROBOTIC PROSTATECTOMY PACK recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - PACK OPEN HEART CFH recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - CRANIOTOMY PACK recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - ENDOVASCULAR PACK recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - ADULT HEART TRAY SHANDS JACKS recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - GYN LAPAROSCOPY/LAPAROTOMY recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - DAVINCI TRUCUSTOM BUNDLE recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - Onkos Surgical Inc. My3D Personalized Pelvic Implant recall (Onkos Surgical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Personalized pelvic implants inadvertently mixed up and distributed to incorrect customers. - Onkos Surgical Inc. My3D Personalized Pelvic Implant recall (Onkos Surgical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Personalized pelvic implants inadvertently mixed up and distributed to incorrect customers. - Product Name: Nihon Kohden CNS-6200 Series Central Nurse Station recall (Nihon Kohden America LLC)
Medical deviceClass IIReported October 14, 2026 · Due to a cybersecurity issue associate with a NULL Pointer Dereferences vulnerabiity. If exploited would potentially cause disruption of the centralized... - Battle Bandage recall (Safeguard US Operating LLC)
Medical deviceClass IIReported October 14, 2026 · Compression bandage may be degraded, which may cause unwanted foreign material to be introduced inside the wound, which may lead to wound exploration and... - Spectral CT and Spectral CT 7500 RT recall (PHILIPS MEDICAL SYSTEMS)
Medical deviceClass IIReported October 14, 2026 · Software issues may affect the safety and performance of Spectral CT system(s). The issues may result in image artifacts, wrong slice thickness, or unintended... - Brand Name: ADAPTABLE Beach Chair Product Name: Beach Chair surgical patient... recall (QUANTUM OPS Inc)
Medical deviceClass IIReported October 14, 2026 · Due to a manufacturing issue (inadequate weld) for patient head positioning system. - Generic Name: Kit recall (Medical Action Industries, Inc. 306)
Medical deviceClass IIIReported October 14, 2026 · An internal data-entry error caused kit lot 333606 to be labeled with an expiration date of March 31, 2027, instead of February 28, 2027. - Sweet Sensi Elevated Edibles Hybrid Gum Drops - Passion Guava Kush 140mg THC. Product... recall (SWEET SENSI)
FoodClass IIReported October 14, 2026 · Staphylococcus aureus detected in product. - biQ-FEL recall (A&P CREATIONS)
FoodClass IReported October 14, 2026 · Product contains undeclared Sildenafil and Tadalafil. - X10 Natural Enhancement Supplement recall (A&P CREATIONS)
FoodClass IReported October 14, 2026 · Product contains undeclared Sildenafil and Tadalafil. - Lemon Alfredo Fettuccine packed in a yellow plastic sealed bag with pink and black... recall (GIAS FOOD INC.)
FoodClass IReported October 14, 2026 · Contamination with Listeria monocytogenes - Berlin Seeds Alfalfa Sprouting Seeds recall (Berlin Seeds)
FoodClass IReported October 14, 2026 · Product contains alfalfa seed recalled by the supplier due to potential E. coli and/or Salmonella contamination. - Donutful Chocolate Dipped Vanilla Cake Donuts - 7.05oz/10ct.Case Configuration 5... recall (The Better Bakehouse Snack Company)
FoodClass IReported October 14, 2026 · Undeclared Milk. - Tri-Immune Boost recall (Centric Compounding LLC)
DrugNot Yet ClassifiedReported October 14, 2026 · Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin. - Apothecary NAD+ Injection 200 mg/mL recall (Apothecary Pharma LLC)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility - Tirzepatide Injection recall (Apothecary Pharma LLC)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility - Tretinoin Cream UPS recall (SUN PHARMACEUTICAL INDUSTRIES INC)
DrugClass IIIReported October 14, 2026 · Failed Impurities/Degradation Specifications - Tretinoin Cream USP recall (SUN PHARMACEUTICAL INDUSTRIES INC)
DrugClass IIIReported October 14, 2026 · Failed Impurities/Degradation Specifications - Tretinoin Cream USP recall (SUN PHARMACEUTICAL INDUSTRIES INC)
DrugClass IIIReported October 14, 2026 · Failed Impurities/Degradation Specifications - Tri-MIX recall (Carolina Infusion, LLC)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility: Related to formulation using bacteriostic water; Related to processing equipment used in compounded product. - Tri-MIX recall (Carolina Infusion, LLC)
DrugClass IIReported October 14, 2026 · Lack of Assurance of Sterility: Related to formulation using bacteriostic water; Related to processing equipment used in compounded product.