Recalls distributed in Hawaii
These notices name Hawaii in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.
1,551 stored notices name Hawaii, reported between Jun 27, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Hawaii too — those are in the archive.
Reported Oct 3, 2018
ESSENTIO Pacemaker
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
5 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 3, 2018
FP0191, Confidence, Bone-Lock WITHGENISTEIN AND CHLOROPHYLL, A Dietary Supplement, 60 tablets per bottle, UPC: 8 92483…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Confidence Inc./Confidence U.S.A. Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Oct 3, 2018
Discovery MR750w Nuclear Magnetic Resonance Imaging System labeled as the following product name sold under: Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems, LLC
FDA (openFDA device enforcement)
Reported Oct 3, 2018
INTEGRIS Allura 9, System Code 722018 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Electronics North America Corporation
26 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 19, 2018
da Vinci S/Si EndoWrist 8mm Monopolar Curved Scissors Model No. 420179-16 Product Usage: EndoWrist Instruments,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 19, 2018
Affixus¿ Hip Fracture Nail Right 125¿ 9 mm x 280 mm, Item Number: 814309280
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
128 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 12, 2018
Baby Quasar Plus, Light Therapy System, packaging, box, sleeve and user manual. Handheld Wrinkles Reduction Device.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Quasar Bio-Tech, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 5, 2018
FLOSEAL Special Applicator Tips in cartons labeled in part, "Floseal SPECIAL APPLICATOR TIPS***6 x Malleable Tip…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 29, 2018
BD BBL GC-Lect Agar; Cat. No. 297715 The device is a selective medium providing enhanced growth and recovery of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported Aug 29, 2018
ELEKTA Digital Accelerator under the following brand names: Elekta Synergy, Synergy S, Synergy Platform, Precise…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 29, 2018
GE Healthcare Revolution EVO, Optima CT660, Optima CT670, Optima CT680. The systems are intended for head, whole body,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare Japan Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 29, 2018
Liebel-Flarsheim Hydra Vision Urology X-Ray System (DR) Liebel-Flarsheim urology systems facilitate radiologic and/or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Liebel-Flarsheim Company LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 22, 2018
HANDS-OFF Multi-Lumen Central Venous Catheter with Blue FlexTip for use only with Arrow One-Piece Percutaneous Sheath…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arrow International Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 15, 2018
AirLife Resuscitation Device, Adult labeled as the following: a. Adult, with mask, oxygen reservoir bag, Part Number…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Vyaire Medical
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 15, 2018
Waterpik Sonic-Fusion Professional, Model: SF-02 Product Usage: The device is composed of a unit base and an oral…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Water Pik, Inc.
FDA (openFDA device enforcement)
Reported Aug 8, 2018
Valsartan 80 mg tablets, 90-count bottles (NDC 63629-6922-2), 60-count bottles ( 63629-6922-3), 28-count bottles…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bryant Ranch Prepack Inc.
2 more products in this recall
FDA (openFDA drug enforcement)
Reported Aug 1, 2018
Arctic Sun Temperature Management System, Model 5000. The Arctic Sun¿ 5000 model is a non-invasive, thermal regulating…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Medical Division
FDA (openFDA device enforcement)
Reported Aug 1, 2018
PR4100 Microplate Reader US, Catalog Number 45591587 Product Usage: The PR4100 Microplate Reader is a 96 well…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bio-Rad Laboratories Inc.
FDA (openFDA device enforcement)
Reported Aug 1, 2018
Brivo XR385, model 5215463, Digital Diagnostic Radiographic System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Aug 1, 2018
Leica Microsystems products labeled as the following: Leica M320 Microscope Systems with Article Numbers 10448419,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Microsystems, Inc.
FDA (openFDA device enforcement)
Reported Aug 1, 2018
Valsartan and Hydrochlorothiazide (HCTZ) Tablets, USP 80 mg/12.5 mg tablets, 90 count-count bottle, Rx Only,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teva Pharmaceuticals USA
8 more products in this recall
FDA (openFDA drug enforcement)
Reported Jul 25, 2018
RayStation stand-alone software treatment planning system, RayStation 4.5, RayStation 4.7, RayStation 4.9 (RayPlan 1),…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
FDA (openFDA device enforcement)
Reported Jul 25, 2018
Dimension Vista¿ CTNI Sample Diluent, KD692, SMN# 10445205
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 25, 2018
Odwalla Superfood fruit smoothie 15.2 oz. (450mL) plastic bottle; Sold in 8 pack case Unit UPC: 000-14054-06405-5…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Coca-Cola Company
FDA (openFDA food enforcement)
Free recall alerts
Get alerted about new Hawaii recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.
Other states
RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.