State

Hawaii product recalls

73,596 recalls have nationwide distribution and so reach Hawaii. 2,772 additional recalls listed Hawaii specifically in their distribution scope.

What the numbers show

Total: 2,772
Critical: 331
Severe: 717
Most recent: 2026-10-14

Of the 2,772 recalls naming Hawaii we have scored against our rubric, 331 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 717 (26%) are Severe.

Which agencies issued them

These figures cover only the 2,772 recalls whose distribution notice names Hawaii specifically. The 73,596 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

26701–26725 of 76368

HighFDA (Devices)·Z-1108-2021·2021-02-17
Helena Laboratories Recalls Cascade Abrazo aPTT Test Cards for Clot Time Issues
Helena Laboratories is recalling Cascade Abrazo aPTT Test Cards due to intermittent potential for shorter than expected clot times.
Product
Cascade Abrazo aPTT Test Card - Product Usage: are to be used with the Cascade Abrazo analyzer and are intended for the determination of the activated Partial Thromboplastin Time (aPTT) of citrated whole blood or plasma, Model 5722, For Export Only.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1016-2021·2021-02-17
Aomori Olympus Recalls ForceMax Endoscopic Injectors Due to Seal Defects
Aomori Olympus is recalling ForceMax endoscopic injectors because some sterile packages have inadequate seals, which could lead to patient infection.
Product
INJECTOR FORCEMAX LOWER 23G 3MM, model no. NM-400U-0323 - Product Usage: Used with endoscopes to perform endoscopic injection for the treatment of esophageal and gastric varices and for submucosal injection in the digestive tract.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1020-2021·2021-02-17
Aomori Olympus Recalls ForceMax Lower Injectors Due to Seal Defects
Aomori Olympus is recalling ForceMax Lower injectors because some sterile packages have inadequate seals, posing an infection risk if used.
Product
INJECTOR FORCEMAX LOWER 23G 6MM 5/BX, model no. NM-400U-0623 - Product Usage: Used with endoscopes to perform endoscopic injection for the treatment of esophageal and gastric varices and for submucosal injection in the digestive tract.
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·21081·2021-02-17
Jimco Recalls J Hunt Home Accent Tables Due to Shock Hazard
Jimco Lamp is recalling J Hunt Home accent tables with charging receptacles due to a shock hazard caused by reverse polarity. No injuries have been reported.
Product
J Hunt Home and J Hunt and Co. Accent Tables with Charging Receptacles
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0963-2021·2021-02-17
Aomori Olympus Recalls B7-2C Balloon Catheters Due to Seal Defects
Aomori Olympus is recalling B7-2C Balloon Catheters because some sterile packages have inadequate seals, which could allow non-sterile equipment to be used and lead to patient infection.
Product
B7-2C BALLOON CATHETER 13mm dia 2.8; model no. B7-2C - Product Usage: Used with endoscopes to inject contrast medium or other medical fluid into the bile duct, pancreatic duct, and respiratory organs.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0959-2021·2021-02-17
Prytime Medical REBOA Catheter Introducer Kit Recalled for Incorrect Needle Size
Prytime Medical Devices is recalling REBOA Catheter Introducer Kits because they may contain a 21G needle instead of the correct 18G needle, which could cause procedure delays or injury.
Product
PRYTIME MEDICAL REBOA Catheter Introducer Kit, REF: KT1835C, Contents: Needle, 18 GA x 7 CM ECHOGENIC, STERILE, 1 EA, SYRINGE, 30CC, STERILE 1 EA, INTRODUCER SHEATH KIT, 7 FR W/.035 SHORT GUIDEWIRE, STERILE 1 EA., PREFILLED, STERILE FIELD SALINE SYRINGE, 10 ML, 4 EA, CLAMP, 5…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1090-2021·2021-02-17
Cardinal Health Recalls Lab Coats and Gowns Due to Defects
Cardinal Health is recalling approximately 29.8 million lab coats and isolation gowns due to potential rips, holes, and foreign material.
Product
Lab Coats SMS X-Large Blue, SKU 2203LC Cardinal Health Isolation Gown, Lab Coat, and Kendall" Gowns are intended to provide minimal barrier protection to protect health care patients and health care personnel from the transfer of microorganisms, body fluids and particulate…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1096-2021·2021-02-17
Cardinal Health Recalls Isolation Gowns Due to Manufacturing Defects
Cardinal Health is recalling isolation gowns and lab coats due to potential rips, holes, or foreign material that may compromise barrier protection.
Product
Gown Kendall Blue L, SKU CT5100, CT5101 Cardinal Health Isolation Gown, Lab Coat, and Kendall" Gowns are intended to provide minimal barrier protection to protect health care patients and health care personnel from the transfer of microorganisms, body fluids and particulate…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1079-2021·2021-02-17
Cardinal Health Recalls Chembloc Preparation Kits Due to Gown Defects
Cardinal Health is recalling Chembloc Preparation and Administration Kits because the included gowns may have rips, holes, or foreign material.
Product
CHEMOBLOC Preparation and Administration Kit, Extra Large Blue Gown, Medium and Large Gloves, Nonsterile, SKU DP5106K
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1107-2021·2021-02-17
Phadia Recalls EliA dsDNA Well Kits Due to Potential False Positive Results
Phadia US Inc is recalling EliA dsDNA Well kits because decreased positive control values may cause false positive test results for systemic lupus erythematosus.
Product
EliA dsDNA Well - Product Usage: intended for the In-Vitro quantitative measurement of IgG antibodies directed to dsDNA in human serum and plasma as an aid in the clinical diagnosis of systemic lupus erythematosus (SLE). Material Number: 14-5500-01
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0956-2021·2021-02-17
ICU Medical Recalls Smallbore Intravascular Administration Sets Due to Filter Assembly Error
ICU Medical is recalling 7,500 smallbore intravascular administration sets because of an incorrect filter assembly. The affected lots were distributed nationwide and in Belgium.
Product
60" (152 cm) Appx 1.9 ml, Smallbore Ext Set w/MicroClave¿ Clear, 1.2 Micron Filter, 2 Clamps, Luer Lock REF MC330174 - Product Usage: The intravascular administration set is a single use, sterile, non pyrogenic device, which provides access for the administration of fluids from…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1095-2021·2021-02-17
Cardinal Health Recalls Kendall Blue Isolation Gowns Due to Defects
Cardinal Health is recalling Kendall Blue Isolation Gowns due to potential rips, holes, or foreign material that may compromise barrier protection.
Product
Gown Kendall Blue RG, SKU CT5000 Cardinal Health Isolation Gown, Lab Coat, and Kendall" Gowns are intended to provide minimal barrier protection to protect health care patients and health care personnel from the transfer of microorganisms, body fluids and particulate material…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1083-2021·2021-02-17
Cardinal Health Recalls ChemoPlus Chemo Prep and Admin Kits
Cardinal Health is recalling ChemoPlus Chemo Prep & Admin Kits because the included gowns may have defects like rips, holes, or foreign material.
Product
ChemoPlus" Chemo Prep & Admin Kit, CT4025
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1081-2021·2021-02-17
Cardinal Health Recalls ChemoPlus Drug Spill Kits Due to Gown Defects
Cardinal Health is recalling ChemoPlus Drug Spill Kits because the included gowns may have rips, holes, or foreign material.
Product
ChemoPlus Drug Spill Kit-INSTI, SKU DP5016K
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1091-2021·2021-02-17
Cardinal Health Recalls Lab Coats and Gowns Due to Manufacturing Defects
Cardinal Health is recalling approximately 29.8 million lab coats and isolation gowns due to potential manufacturing defects such as rips, holes, and foreign material.
Product
Lab Coats SMS 2X-Large Blue, SKU 2204LC Cardinal Health Isolation Gown, Lab Coat, and Kendall" Gowns are intended to provide minimal barrier protection to protect health care patients and health care personnel from the transfer of microorganisms, body fluids and particulate…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1082-2021·2021-02-17
Cardinal Health Recalls Kendall Spill Kits Due to Gown Defects
Cardinal Health is recalling Kendall Spill Kits because the included gowns may have rips, holes, or foreign material.
Product
Kendall Spill Kit, 6 Per Case, NonsterileI, BB6016K
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1094-2021·2021-02-17
Cardinal Health Recalls Lab Coats and Gowns Due to Defects
Cardinal Health is recalling approximately 29.8 million lab coats and isolation gowns due to potential defects like rips, holes, and foreign material.
Product
Lab Coats SMS 2X-Large White, SKU 2304LC Cardinal Health Isolation Gown, Lab Coat, and Kendall" Gowns are intended to provide minimal barrier protection to protect health care patients and health care personnel from the transfer of microorganisms, body fluids and particulate…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1089-2021·2021-02-17
Cardinal Health Recalls Lab Coats and Gowns Due to Manufacturing Defects
Cardinal Health is recalling approximately 29.8 million lab coats and isolation gowns due to potential rips, holes, and foreign material that may compromise barrier protection.
Product
Lab Coats SMS Large Blue, SKU 2202LC Cardinal Health Isolation Gown, Lab Coat, and Kendall" Gowns are intended to provide minimal barrier protection to protect health care patients and health care personnel from the transfer of microorganisms, body fluids and particulate…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1080-2021·2021-02-17
Cardinal Health Recalls ChemoPlus Drug Spill Kits Due to Gown Defects
Cardinal Health is recalling ChemoPlus Drug Spill Kits because the included gowns may have rips, holes, or foreign material.
Product
CHEMOPLUS DRUG SPILL KIT HOS, SKU CT4004
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1086-2021·2021-02-17
Cardinal Health Recalls Isolation Gowns Due to Potential Rips and Holes
Cardinal Health is recalling isolation gowns and lab coats because they may have rips, holes, or open seams that compromise barrier protection.
Product
Gown Isolation W/Ties Xl Ylw, SKU 1101PG Cardinal Health Isolation Gown, Lab Coat, and Kendall" Gowns are intended to provide minimal barrier protection to protect health care patients and health care personnel from the transfer of microorganisms, body fluids and particulate…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1078-2021·2021-02-17
Cardinal Health Recalls Chemo Spill Kits Due to Gown Defects
Cardinal Health is recalling 137,346 ChemoPlus Chemo Spill Kits because the included gowns may have rips, holes, or foreign material.
Product
Covidien ChemoPlus Chemo Spill Kit, Nonsterile, SKU DP5108K
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0957-2021·2021-02-17
ICU Medical Recalls MicroCLAVE Intravascular Administration Sets Due to Filter Assembly Error
ICU Medical is recalling 7,500 MicroCLAVE intravascular administration sets due to incorrect filter assembly. The affected lots were distributed nationwide in the U.S. and in Belgium.
Product
7 IN (18cm) APPX 0.43ml, SMALLBORE SET, MicroCLAVE, FILTER SetSource - Product Usage: The intravascular administration set is a single use, sterile, non pyrogenic device, which provides access for the administration of fluids from a container to a patient s vascular system…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1106-2021·2021-02-17
Arrow AGB+ Multi-Lumen CVC Kit Recalled for Labeling Error
Arrow International Inc. is recalling 1,705 kits due to a potential product code mislabeling that could cause delays or allergic reactions in sensitive patients.
Product
Arrow AGB+ Multi-Lumen CVC Kit 7Fr 3 Lumen- Intended for venous access to the central circulation by the way of the femoral, jugular, or subclavian veins. Product Code: CDC-45703-1A
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1097-2021·2021-02-17
Cardinal Health Recalls Kendall Blue XXL Gowns Due to Defects
Cardinal Health is recalling Kendall Blue XXL gowns due to potential rips, holes, or foreign material that may compromise barrier protection.
Product
Gown Kendall Blue XXL, SKU CT5102 Cardinal Health Isolation Gown, Lab Coat, and Kendall" Gowns are intended to provide minimal barrier protection to protect health care patients and health care personnel from the transfer of microorganisms, body fluids and particulate…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1087-2021·2021-02-17
Cardinal Health Recalls Isolation Gowns Due to Potential Rips and Holes
Cardinal Health is recalling isolation gowns and lab coats due to potential defects like rips, holes, and open seams that may compromise barrier protection.
Product
Gown Isolation W/Ties Univ Blu, SKU 1200PG, 2200PG, 552200PG Cardinal Health Isolation Gown, Lab Coat, and Kendall" Gowns are intended to provide minimal barrier protection to protect health care patients and health care personnel from the transfer of microorganisms, body…
Category
Medical Device
Distribution
Distributed nationwide