Recalls in Hawaii (page 17)

3886 recalls.

• Vevor Recalls Baby Loungers Due to Risk of Serious Injury or Death from Entrapment and Fall Hazards; Violate Mandatory Standard for Infant Sleep Products
  Consumer productReported July 3, 2026 · The recalled baby loungers violate the mandatory safety standard for infant sleep products. The sides are too low to contain an infant and the enclosed...
• Dried Herring Fish 7 oz. recall (Prime Food Processing LLC.)
  FoodClass IReported July 1, 2026 · Improperly eviscerated which may result in Clostridium botulinum contamination
• 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...
• 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.
• Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
  Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
• Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
  Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
• Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
  Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
• Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
  Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
• Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
  Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
• Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
  Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
• Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
  Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
• Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. KIT... recall (Medline Industries, LP)
  Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
• Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
  Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
• Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
  Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
• Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
  Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
• Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
  Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
• Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. DR... recall (Medline Industries, LP)
  Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
• Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
  Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
• Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
  Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
• Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
  Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
• 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.
• Philips Telemetry Monitor 5500 1.4 GHz. Model Number: 867232. Includes the following... recall (Philips North America Llc)
  Medical deviceClass IIReported July 1, 2026 · Potential for device reset to default "NEW_DEVICE" state, which may lead to a to loss of device configuration and the equipment label, resulting in a failure...
• 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...
• 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).
• 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).
• 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...
• 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.
• 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...
• 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...
• 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.

← NewerOlder →