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.
1,584 stored notices name Hawaii, reported between Jun 27, 2012 and Nov 18, 2026. A further 48,784 notices were distributed nationwide, so they reach Hawaii too — those are in the archive.
Reported Sep 7, 2016
FUJIFILM Digital Mammography System Aspire HD (FDR MS-1000) with Biopsy Positioner (FDR-1000BPY) The Fujifilm Digital…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fujifilm Medical Systems U.S.A., Inc.
FDA (openFDA device enforcement)
Reported Aug 31, 2016
Brilliance 64 CT Model number 728231 Product Usage: Computed Tomography X-ray systems intended to produce…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 31, 2016
Infinite F50 instrument. The INFINITE F50 instrument is a 96-well absorbance reader for the measurement of light…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tecan US, Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 24, 2016
Hospira RECEPTAL CANISTERS: 1L(1000mL), 1.5L(1500mL), 2L(2000mL) Canister, ATS, 2000, with Valve 1) List Numbers…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hospira Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 17, 2016
NucliSENS easyMAG Magnetic Silica The NucliSENS easyMAG accessory products are reagents and disposable to be used with…
High riskUsing this product could cause serious injury, illness or death — stop using it now.BioMerieux SA
FDA (openFDA device enforcement)
Reported Aug 10, 2016
ONLINE TDM Vancomycin 100 tests; ONLINE TDM Vancomycin 200 tests; Hitachi Vancomycin (Modular P); Hitachi Vancomycin…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Aug 10, 2016
Zimmer¿ Air Dermatome II Handpiece, item number 00-8851-001-00. The Zimmer Air Dermatome II handpiece and width plates…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Surgical Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 3, 2016
Babytherm 8004/8010, Infant Warmer, Class II device, 510 K K971198, Catalog # FR00105 (Babytherm 8010), 2M30404…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Draeger Medical, Inc.
FDA (openFDA device enforcement)
Reported Aug 3, 2016
Xtra Immunity Brown Rice Antioxidant Probiotic Extract, a liquid packaged in a 500mL bottle. UPC 184368000114. The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sustainable Community Development LLC dba SCD Probiotics
FDA (openFDA food enforcement)
Reported Jul 27, 2016
Mountain Thins Trail Mix flavor, packaged in a stand-up film pouch (resealable), net wt. 5.3 oz. The UPC is 0 41770…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Brown & Haley Inc.
FDA (openFDA food enforcement)
Reported Jul 27, 2016
ATEC CANISTER. Suction Canister with Lid 490 cc., RX Only; Suction canister used to collect fluid during a breast…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hologic, Inc.
FDA (openFDA device enforcement)
Reported Jul 27, 2016
Kellogg's Special K Mini Brownies Blondie, 6 ct, 4.44 oz.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kellogg Company
24 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 27, 2016
RayStation 3.0, RayStation 3.5, RayStation 4.0, RayStation 4.5, RayStation 4.7 and RayStation 5 --- Radiation Therapy…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
FDA (openFDA device enforcement)
Reported Jul 27, 2016
Depuy Synthes Trauma- Trochanteric Fixation Nail Advanced (TFNA) Blade/Screw Guide Sleeve, Surgical Instrument Part…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
FDA (openFDA device enforcement)
Reported Jul 27, 2016
HX2" Temperature Management Systems; The Terumo¿ HX2" Temperature Management System provides temperature control of two…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 20, 2016
Duloxetine Delayed-Release Capsules, USP, 20 mg, 60-count bottles, Rx only, Manufactured by Apotex Inc, Toronto,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Apotex Scientific, Inc.
2 more products in this recall
FDA (openFDA drug enforcement)
Reported Jul 20, 2016
The LifeCare PCA Plus II infusion pump system is designed for safe, effective, analgesic delivery to patients through…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hospira Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 20, 2016
cobas¿ Liat Influenza A/B Quality Control Kit; For use with cobas¿ Liat Influenza A/B Assay.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Roche Molecular Systems, Inc.
FDA (openFDA device enforcement)
Reported Jul 20, 2016
6.5 mm Cannulated Screw, Product code HWC, Device Listing Number D028949, Screw, Fixation Bone Product Usage: Intended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
17 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 13, 2016
The System 83 Plus, Endoscope Washer/Disinfector Designed for the simultaneous reprocessing of up to two flexible…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Custom Ultrasonics, Inc.
FDA (openFDA device enforcement)
Reported Jul 13, 2016
Novation Press-Fit Splined RDD, Extended Offset, HA Coated, 12/14 Taper Femoral Stems, Size 17. Product Usage Femoral…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 13, 2016
GE Healthcare, Discovery MR750w
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Jul 13, 2016
Natural Directions Organic Mixed Vegetables, frozen, net wt. 12 oz. UPC 0 15400 19672 7
High riskUsing this product could cause serious injury, illness or death — stop using it now.Norpac Foods, Inc. (Plant #8)
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jul 13, 2016
All 4-aminopyridine Products, Rx Only, Compounded by RELIABLE DRUG/RELIABLE COMPOUNDING PHARMACY, 801 Irving St., SAN…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Reliable Rexall-A Compounding Pharmacy
69 more products in this recall
FDA (openFDA drug 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.