Recalls in California (page 18)
4209 recalls.
- Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - INZONE DETACHMENT SYSTEM recall (Stryker Neurovascular)
Medical deviceClass IIReported July 1, 2026 · Embolization coil detachment system devices may experience premature battery drain causing devices to: 1) Not power on; 2) Power on with faint audible and... - Acumed Hexalob Screw various sizes: REF Numbers: : 3070-27008 2.7mm x 8mm NL Hexalobe... recall (Acumed LLC)
Medical deviceClass IIReported July 1, 2026 · Due to manufacturing error, hexalobe screws used with wrist fixation system may break during use. - Philips Avalon Fetal Monitor recall (Philips North America Llc)
Medical deviceClass IIReported July 1, 2026 · Monitor has incorrect assembly of the speaker connector which can cause device cables to be pulled out of the housing and increase the risk of intermittent or... - Philips Avalon Fetal Monitor recall (Philips North America Llc)
Medical deviceClass IIReported July 1, 2026 · Monitor has incorrect assembly of the speaker connector which can cause device cables to be pulled out of the housing and increase the risk of intermittent or... - Da Vinci ASSY recall (Intuitive Surgical, Inc.)
Medical deviceClass IIReported July 1, 2026 · Operative components of surgical systems potentially distributed with E-brake retainer pin, so in event of a structural column failure, the E-brake pin would... - Spring & Mulberry Blood Orange Date-Sweetened Chocolate recall (Spring & Mulberry Inc.)
FoodClass IReported July 1, 2026 · Potential Salmonella contamination - Spring & Mulberry Coffee Date-Sweetened Chocolate recall (Spring & Mulberry Inc.)
FoodClass IReported July 1, 2026 · Potential Salmonella contamination - Spring & Mulberry Sea Salt Date-Sweetened Chocolate recall (Spring & Mulberry Inc.)
FoodClass IReported July 1, 2026 · Potential Salmonella contamination - 1) Spring & Mulberry Pure Dark Date-Sweetened Chocolate recall (Spring & Mulberry Inc.)
FoodClass IReported July 1, 2026 · Potential Salmonella contamination - Spring & Mulberry Pecan Date Date-Sweetened Chocolate recall (Spring & Mulberry Inc.)
FoodClass IReported July 1, 2026 · Potential Salmonella contamination. - Spring & Mulberry Mulberry Fennel Date-Sweetened Chocolate recall (Spring & Mulberry Inc.)
FoodClass IReported July 1, 2026 · Potential Salmonella contamination. - Spring & Mulberry Mango Chili Date-Sweetened Chocolate recall (Spring & Mulberry Inc.)
FoodClass IReported July 1, 2026 · Potential Salmonella contamination - Spring & Mulberry Lavender Rose Date-Sweetened Chocolate recall (Spring & Mulberry Inc.)
FoodClass IReported July 1, 2026 · Potential Salmonella contamination - Spring & Mulberry Earl Grey Date-Sweetened Chocolate recall (Spring & Mulberry Inc.)
FoodClass IReported July 1, 2026 · Potential Salmonella contamination - Spring & Mulberry Mixed Berry Date-Sweetened Chocolate recall (Spring & Mulberry Inc.)
FoodClass IReported July 1, 2026 · Potential Salmonella contamination - Spring & Mulberry Mint Leaf Date-Sweetened Chocolate recall (Spring & Mulberry Inc.)
FoodClass IReported July 1, 2026 · Potential Salmonella contamination - Motor City Pizza Co. 5 Cheese Bread Single retail pack recall (Champion Foods, LLC)
FoodClass IIReported July 1, 2026 · potential salmonella contamination - Perampanel CIII Tablets recall (SUN PHARMACEUTICAL INDUSTRIES INC)
DrugClass IIReported July 1, 2026 · Labeling: Label Mix-up: 10mg Perampanel CIII tablet was found in a Perampanel CIII bottle labeled Perampanel 6 mg tablets. - Povi-One recall (Elevate Oral Care)
DrugClass IIReported July 1, 2026 · sub potency - Lacosamide Tablets recall (Annora Pharma Private Limited)
DrugClass IIReported July 1, 2026 · Presence of a Foreign Tablets: Complaint received, possible mix-up of Selexipag 1000 mcg tablet in a bottle of Lacosamide Tablets USP, 100mg. - BD ChloraPrep FREPP Clear recall (CareFusion 213, LLC)
DrugClass IReported July 1, 2026 · Non-Sterility: Due to presence of Aspergillus penicillioides. And Lack of Assurance of Sterility: Due to wrinkles in the paper lidding which may breach the... - BD ChloraPrep Clear recall (CareFusion 213, LLC)
DrugClass IReported July 1, 2026 · Non-Sterility: Due to presence of Aspergillus penicillioides. - BD ChloraPrep FREPP Clear recall (CareFusion 213, LLC)
DrugClass IIReported July 1, 2026 · Lack of Assurance of Sterility: Due to wrinkles in the paper lidding which may breach the seal area. - BD ChloraPrep Clear recall (CareFusion 213, LLC)
DrugClass IIReported July 1, 2026 · Lack of Assurance of Sterility: Due to wrinkles in the paper lidding which may breach the seal area. - hydrOXYzine Hydrochloride Oral Solution recall (ANI Pharmaceuticals, Inc.)
DrugClass IIIReported July 1, 2026 · Presence of foreign substance - DULOXETINE D/R recall (Direct Rx)
DrugClass IIReported July 1, 2026 · CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit - Sensipar recall (Amgen, Inc.)
DrugClass IIReported July 1, 2026 · CGMP Deviations - Corlanor recall (Amgen, Inc.)
DrugClass IIReported July 1, 2026 · Presence of Foreign Substance. - Sensipar recall (Amgen, Inc.)
DrugClass IIReported July 1, 2026 · CGMP Deviations - Sensipar recall (Amgen, Inc.)
DrugClass IIReported July 1, 2026 · CGMP Deviations - Corlanor recall (Amgen, Inc.)
DrugClass IIReported July 1, 2026 · Presence of Foreign Substance. - Fenofibrate Capsules recall (Ajanta Pharma USA Inc)
DrugClass IIReported July 1, 2026 · CGMP Deviations - Carton Label: MAJOR recall (The Harvard Drug Group LLC)
DrugClass IIReported July 1, 2026 · Subpotent Drug - Abiomed Impella CP Set with SmartAssist recall (Abiomed, Inc.)
Medical deviceClass IReported July 1, 2026 · Potential for thrombus formation during prolonged use of the introducer. - Abiomed Impella CP Set with SmartAssist recall (Abiomed, Inc.)
Medical deviceClass IReported July 1, 2026 · Potential for thrombus formation during prolonged use of the introducer. - Abiomed 14 Fr x 25 cm Low Profile Introducer Kit for Impella CP. Impella Set Product... recall (Abiomed, Inc.)
Medical deviceClass IReported July 1, 2026 · Potential for thrombus formation during prolonged use of the introducer. - Abiomed 14 Fr x 13 cm Low Profile Introducer Kit for Impella CP. Impella Set Product... recall (Abiomed, Inc.)
Medical deviceClass IReported July 1, 2026 · Potential for thrombus formation during prolonged use of the introducer. - Intera Oncology INTERA 3000 Hepatic Artery Infusion Pump recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 1, 2026 · There is the potential for leakage along the drug pathway from the pump through the end of the catheter. - Octopus 4 Tissue Stabilizer recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported July 1, 2026 · During the manufacturing process, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to... - Octopus Evolution AS Tissue Stabilizer recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported July 1, 2026 · During the manufacturing process, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to... - Octopus Evolution Tissue Stabilizer recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported July 1, 2026 · During the manufacturing process, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to... - Thuvera Laser Console. Software Version 2.2. Portable Thulium Fiber Laser. recall (IPG Medical Corporation)
Medical deviceClass IIReported July 1, 2026 · Software anomaly that causes a false display of error code 5018. - GE Healthcare AW Server 3.2 ext.6.5 recall (GE Medical Systems SCS)
Medical deviceClass IIReported July 1, 2026 · GE HealthCare has become aware of a context synchronization issue in AW Server 3.2 ext. 6.5. When a user selects a patient or exam in the AW Server Web Client... - Off-Axis Alliance Glenoid recall (Zimmer, Inc.)
Medical deviceClass IIReported July 1, 2026 · Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage. - Off-Axis Alliance Glenoid recall (Zimmer, Inc.)
Medical deviceClass IIReported July 1, 2026 · Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage. - Off-Axis Comprehensive Shoulder System recall (Zimmer, Inc.)
Medical deviceClass IIReported July 1, 2026 · Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage. - Off-Axis Comprehensive Shoulder System recall (Zimmer, Inc.)
Medical deviceClass IIReported July 1, 2026 · Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage. - Off-Axis Comprehensive Shoulder System Small recall (Zimmer, Inc.)
Medical deviceClass IIReported July 1, 2026 · Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage. - Multi-Snare Set: 5 mm x 125 cm recall (PFM MEDICAL INC.)
Medical deviceClass IIReported July 1, 2026 · A snare catheter including luer lock, indicated for removal or manipulation of a foreign body in the vascular system, failed to meet the biocompatibility... - VOCSN+Pro package recall (Ventec Life Systems, Inc.)
Medical deviceClass IIReported July 1, 2026 · Respiratory system intended to provide continuous/intermittent ventilator support, may have a damaged back-up battery supporting backup alarm function, which... - TMJ Bilateral Implants recall (TMJ Solutions Inc)
Medical deviceClass IIReported July 1, 2026 · Custom temporomandibular joint implant may have contained incorrect patient-specific components that led to a poor fit of the implant, leading to a right-sided... - Medline Convenience Kits: 1) DRAWER 6A ADULT CENTRAL LINE recall (Medline Industries, LP)
Medical deviceClass IReported July 1, 2026 · The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose... - Medline Convenience Kits: 1) DRAWER 6 CENTRAL LINE INSERTIO recall (Medline Industries, LP)
Medical deviceClass IReported July 1, 2026 · The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose... - Medline Convenience Kits: 1) OPEN HEART CDS recall (Medline Industries, LP)
Medical deviceClass IReported July 1, 2026 · The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose... - Medline Convenience Kits: 1) DYNJ905503F recall (Medline Industries, LP)
Medical deviceClass IReported July 1, 2026 · The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose... - Combination Smoke and Carbon Monoxide (CO) Detectors Recalled Due to Risk of Serious Injury or Death from Failure to Alert Consumers to Fire; Sold Exclusively on Amazon.com by Treatlife Technology
Consumer productReported June 30, 2026 · The recalled detectors can fail to alert consumers of a fire, posing a risk of serious injury or death from smoke inhalation or burns. - Daikin Comfort Technologies Manufacturing Recalls Amana Air Conditioners and Heat Pumps Due to Risk of Serious Injury from Fire and Burns
Consumer productReported June 30, 2026 · The heating element can remain energized during a ground fault, despite being turned off, posing a risk of fire or burn injury to consumers. - Honlyne LED Party Favors Recalled Due to Risk of Serious Injury Death from Battery Ingestion; Violate Mandatory Standard for Consumer Products with Button Cell Batteries; Sold by Huizhou Rongheng Network Technology
Consumer productReported June 30, 2026 · The LED party favors violate the mandatory safety standard for consumer products because the battery compartment within the light-up products contains button... - Montessori Busy Board Toys Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion; Violate Mandatory Standard for Toys; Sold on Amazon by Small Fish
Consumer productReported June 30, 2026 · The busy boards violate the mandatory safety standard for toys because magnets can detach, posing a deadly ingestion hazard. When high-powered magnets are... - Raychy Children's Light Sneakers Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Consumer Products with Coin Batteries; Imported by Carina and Rambo
Consumer productReported June 30, 2026 · The recalled sneakers violate the mandatory standard for consumer products with button cell and coin batteries because the lithium coin batteries can be... - Shield Line Recalls MedPride Baby Oil Bottles Due to Risk of Serious Injury or Death from Child Poisoning; Violate Mandatory Standard for Child-Resistant Packaging
Consumer productReported June 30, 2026 · The baby oil contains low-viscosity hydrocarbons, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The baby... - Southern Telecom Expands Recall of Lomi Waxing Kits Due to Risk of Serious Injury or Death from Fire and Burn Hazards; Additional Model and Reported Incidents
Consumer productReported June 30, 2026 · The roll-on warmers' power cord can overheat and short circuit, posing a risk of serious injury or death from fire, burn and electrical shock hazards. - Super Off-Road Solar Power Banks Recalled Due to Overheating; Imported by Spector & Co.
Consumer productReported June 30, 2026 · The solar power bank's lithium-ion battery can swell and overheat, posing a burn hazard to consumers. - Yamazuki Recalls Youth All-Terrain Vehicles (ATVs) Due to Risk of Serious Injury or Death from Crash; Violate Mandatory Standard for ATVs
Consumer productReported June 30, 2026 · The recalled youth ATVs violate the mandatory safety standard for ATVs because they are missing brake lights, reducing visibility of the youth ATV to other... - Kith Retail Recalls Children's Loungewear Sets Due to Risk of Serious Injury from Burn Hazard; Violate Mandatory Standards for Children's Sleepwear
Consumer productReported June 30, 2026 · The recalled children's loungewear sets violate the mandatory flammability standards for children's sleepwear, posing a risk of serious burn injuries. - azuma foods TAKO WASABI Seasoned Octopus with Wasabi PERISHABLE/KEEP FROZEN PRODUCT... recall (Azuma Foods International Inc USA)
FoodClass IReported June 24, 2026 · Undeclared fish. - Great Value Hawaiian Roll 4pk recall (United States Bakery)
FoodClass IIReported June 24, 2026 · Firm observed oily and sticky substance on direct food contact surface packaging of finished product. - Brand Name: HeartMate Product Name: HM 11V Li-ion Backup Battery recall (Thoratec LLC)
Medical deviceClass IIReported June 24, 2026 · Due to 11 volt Backup Battery failures. - Brand Name: HeartMate Product Name: HeartMate 3" System Controller Model/Catalog... recall (Thoratec LLC)
Medical deviceClass IIReported June 24, 2026 · Due to 11 volt Backup Battery failures. - Brand Name: HeartMate Product Name: HeartMate 3 Left Ventricular System recall (Thoratec LLC)
Medical deviceClass IIReported June 24, 2026 · Due to 11 volt Backup Battery failures. - Splashwire Hydrophilic Guide Wire: REF: MSWSTDA35150 UDI-DI codes: 00884450529645 ... recall (Merit Medical Systems, Inc.)
Medical deviceClass IIReported June 24, 2026 · Due to unsealed portions of pouches. - BD Connecta" BD Luer-Lok" 360 REF 394910 UDI-DI code: 00382903949106 BD Connecta"... recall (BD SWITZERLAND SARL)
Medical deviceClass IIReported June 24, 2026 · Due to stopcock issues when using the plastic luer-lok syringe, the connection at the Port C may over thread or continue to spin rather than tightening... - Product Name: STAAR ICL Calculation Software Software Version: Version 8.00 Product... recall (Staar Surgical AG)
Medical deviceClass IIReported June 24, 2026 · Due to a software coding issues for calculating the implant orientation diagram printout for the implantation for toric implantable collamer lenses. - MEDLINE Medical Procedure Kits labeled as: 1) CRANI recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: 1) RETINA LAC/USC CDS recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: KIT URO ROBOT CYSTECTOMY recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as CLOVIS HYSTEROSCOPY recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: 1) D AND C PACK recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as BASIC GYN recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: PELVIC LAP PACK recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: 1) BR L&D PACK recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: 1) CAROTID NEURO PACK recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: NURSING KIT recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: DR FERNANDEZ recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as BIOBURDEN TEST KIT recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: 1) CV DRAPING/BASIN recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: 1) KIT UROLOGY URETHROPLASTY recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: TONSIL PACK CATH recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: 1) CHEST EXPLORATION ECMO recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: CATH 22F ROBINSON STRL 5'S PK recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include...