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 Jul 24, 2013
CDI Blood Parameter Monitoring System 500 with Arterial and Venous blood parameter modules and Hematocrit/Saturation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 17, 2013
da Vinci Si Surgeon Side Cart, model number SS3000; Manufactured by Intuitive Surgical, Sunnyvale, CA 94086. Intuitive…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 17, 2013
Torn and Glasser Brand Roasted & Salted Natural Pistachios, 8 oz. 24/8oz Case. Labeling reads in part:"TORN &…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Torn & Glasser Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jul 10, 2013
HealthLink***BIOPSY PUNCHES*** Disposable manual instrument for skin biopsy.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Clorox Healthcare Holdings, LLC (dba HealthLink)
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 10, 2013
Computed Tomography X-ray systems Product Usage: The Brilliance CT 64, Ingenuity Core, and Ingenuity Core128 scanners…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Jul 3, 2013
DC power cable (p/n 3010556) supplied with the MEDRAD(R) Veris MR Vital Signs Monitor: Product Usage: Monitor,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medrad Inc.
FDA (openFDA device enforcement)
Reported Jun 26, 2013
VITROS Chemistry Products-HCY Reagent packaged in a kit carton. Catalog# 6802002. Used to quantitatively measure total…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics
FDA (openFDA device enforcement)
Reported Jun 26, 2013
GlideScope Video Laryngoscope (GVL) 3, 4, 5 and GlideScope (AVL) 2, 3, 4 and 5 reusable blades Product Usage: The…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Verathon, Inc.
FDA (openFDA device enforcement)
Reported Jun 26, 2013
Zimmer Patient Helper Bed Frame Adapter Assembly The bed frame adapter assembly is intended to be used by qualified…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
FDA (openFDA device enforcement)
Reported Jun 19, 2013
XYMOGEN EP Exclusive Patented Dietary Supplement Artriphen Clinically Tested to Support Healthy Joint Function, 90 and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Atlantic Pro Nutrients, Inc. dba XYMOGEN
FDA (openFDA food enforcement)
Reported Jun 12, 2013
White Farm Enriched White Bread. 16 oz (454g), 9pc/box. UPC 0 10314 10002 0. The label is white with blue and green…
High riskUsing this product could cause serious injury, illness or death — stop using it now.LL Bakery, Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 12, 2013
Comfort brand Ear-Loop Face Mask, Item #: 3100, Model Numbers: # 3100B, # 3100P, # 3100G, # 3100Y, # 3100W; Product is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Maytex Corp.
FDA (openFDA device enforcement)
Reported Jun 12, 2013
REF 8229705 x1 NIM TriVantage EMG Endotracheal Tube 5.0 mm I.D. x 6.5 mm O.D. Medtronic Xomed, Inc., 6743 Southpoint…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medtronic Xomed, Inc.
FDA (openFDA device enforcement)
Reported Jun 5, 2013
Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument - Aliquot Plunger Delivery System, 4", Part…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Orthovita, Inc., dba Stryker Orthobiologics.
12 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 5, 2013
***REF S-3D*** 3mm Diamond Ball. Used for cutting and shaping bone.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Anspach Effort, Inc.
FDA (openFDA device enforcement)
Reported May 29, 2013
Cardinal Health hCG Cassette Rapid Test, Part Number: B1077-22 (Mfg PN: 4582105026) The SP hCG Cassette Rapid Test is a…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Alere San Diego, Inc.
FDA (openFDA device enforcement)
Reported May 29, 2013
Molift Smart 150
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Moller Vital
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 29, 2013
Brilliance CT 16-Slice Water, System Code: 728245; Brilliance CT 10-Slice Water, System Code: 728250; Brilliance CT…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported May 29, 2013
Stryker Orthopaedics Triathlon Femoral Distal Augment- Left; 1 single unit per package Howmedica Osteonics Corp. 325…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Howmedica Osteonics Corp.
FDA (openFDA device enforcement)
Reported May 22, 2013
Proplege Coronary Sinus Catheter model PR9, 11 French Introducer, kitted with PR9. Product Usage: The catheter…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edwards Lifesciences, LLC
FDA (openFDA device enforcement)
Reported May 22, 2013
GE Healthcare Innova 2100 IQ, Innova 3100 IQ, Innova 4100 IQ, Innova 2121 IQ, Innova 3131 IQ , Innova 3100, Innova…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported May 8, 2013
STERRAD CYCLESURE 24 Biological Indicator (BI) The STERRAD CYCLESURE 24 Biological Indicator (BI), is intended to be…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Advanced Sterilization Products
FDA (openFDA device enforcement)
Reported May 8, 2013
Diacap(R) Ultra Dialysis Fluid Filter, Catalog Number 7107367. Intended to filter bacteria and endotoxins from dialysis…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.B. Braun Medical, Inc.
FDA (openFDA device enforcement)
Reported May 1, 2013
all One Active Senior Multiple Vitamin & Mineral Powder dietary supplement, 30 Day Supply, 15.9 oz. canisters
Moderate riskThis product could cause temporary or reversible health problems — stop using it.All One, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
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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.