April 2014 recalls

645 recalls were announced in April 2014.

What the numbers show

Critical: 60
Severe: 167
High: 236
Moderate: 162
Low: 20

Of the 645 recalls this month scored against our rubric, 9% are Critical, 26% are Severe.

Which agencies issued them

601–645 of 645

HighFDA (Devices)·Z-1292-2014·2014-04-02
Teleflex Medical Recalls Non-absorbable Surgical Sutures for Needle Attachment Defect
Teleflex Medical is recalling non-absorbable poly(ethylene terephthalate) surgical sutures because they did not meet minimum needle attachment strength requirements.
Product
Sutures, Non-absorbable, Synthetic, Polyethylene, Sterile, Rx only, Product Usage: Non-absorbable poly(ethylene terephthalate) surgical suture is a multifilament, non-absorbable, sterile, flexible thread prepared from fibers of high molecular weight, long-chain, linear…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1288-2014·2014-04-02
Teleflex Medical Recalls Weck Vista Universal Balloon Open Access Ports
Teleflex Medical is recalling 55,521 units of Weck Vista Universal Balloon Open Access Ports due to reported gas leakage that may delay laparoscopic surgeries.
Product
5/10 Weck¿ Vista" Universal Balloon Open Access Port Short Length (53mm), Product Usage: An endoscope and accessories is a device used to provide access, illumination, and allow observation or manipulation of body cavities, hollow organs, and canals.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1279-2014·2014-04-02
Teleflex Medical Recalls Weck Vista Universal Cannula Due to Gas Leakage
Teleflex Medical is recalling 5/10 mm Weck Vista Universal Cannulas because they may leak insufflation gas, potentially delaying laparoscopic surgeries.
Product
5/10 mm Weck¿, Vista" Universal Cannula, Teleflex Medical, Product Usage: An endoscope and accessories is a device used to provide access, illumination, and allow observation or manipulation of body cavities, hollow organs, and canals.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1302-2014·2014-04-02
BioCardia Recalls Morph AccessPro Steerable Introducers Due to Particulate Risk
BioCardia, Inc. is recalling Morph AccessPro Steerable Introducers because particulates in the inner lumen could cause an embolic event.
Product
Morph AccessPro Steerable Introducer; 6F Introducer, 90 cm working length: Single use only. BioCardia, Inc. San Carlos, CA 94070 BioCardia Morph AccessPro is intended to provide a pathway through medical instruments cush as balloon dilation catheters, guidewires or…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1286-2014·2014-04-02
Teleflex Medical Recalls Weck Vista Universal Balloon Open Access Ports
Teleflex Medical is recalling 55,521 units of Weck Vista Universal Balloon Open Access Ports due to reported gas leakage that may delay laparoscopic surgeries.
Product
5/10 Weck¿ Vista" Universal Balloon Open Access Port - Standard Length (70mm), Product Usage: An endoscope and accessories is a device used to provide access, illumination, and allow observation or manipulation of body cavities, hollow organs, and canals.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1271-2014·2014-04-02
Mevion S250 Proton Radiation Therapy System Recalled for Positioning Error
Mevion Medical Systems is recalling the S250 Proton Radiation Therapy System because a geometric positioning error can occur after rotational corrections are applied to treatment fields.
Product
MEVION S250, System, Radiation Therapy, Charged-Particle, Medical used for Proton Radiation Therapy Product Usage: Proton Radiation Therapy
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1294-2014·2014-04-02
Teleflex Medical Recalls Polyglycolic Acid Sutures for Needle Attachment Defects
Teleflex Medical is recalling 32,271 units of absorbable polyglycolic acid sutures because they failed to meet minimum needle attachment strength requirements.
Product
Sutures, Absorbable, Synthetic, Polyglycolic Acid, Sterile, Rx only, Product Usage: Non-absorbable polypropylene surgical suture is a monofilament, Non-absorbable, sterile, flexible thread prepared from long-chain polyolefin polymer known as polypropylene and is indicated…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1282-2014·2014-04-02
Teleflex Medical Recalls 12mm Weck Vista Cannula Due to Gas Leakage
Teleflex Medical is recalling 12mm Weck Vista Cannulas because they may leak insufflation gas, potentially delaying laparoscopic surgical procedures.
Product
12mm Weck¿ Vista" Cannula-only, Teleflex Medical, Product Usage: An endoscope and accessories is a device used to provide access, illumination, and allow observation or manipulation of body cavities, hollow organs, and canals.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1289-2014·2014-04-02
Teleflex Medical Recalls Weck Vista Universal Balloon Open Access Ports
Teleflex Medical is recalling 55,521 Weck Vista Universal Balloon Open Access Ports due to gas leakage that may delay laparoscopic surgeries.
Product
5/10/12 Weck¿ Vista" Universal Balloon Open Access Port Standard Length (70mm), Product Usage: An endoscope and accessories is a device used to provide access, illumination, and allow observation or manipulation of body cavities, hollow organs, and canals.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1304-2014·2014-04-02
Medtronic Recalls FiberNet Embolic Protection System Due to Manufacturing Defect
Medtronic is recalling specific lots of the FiberNet Embolic Protection System because a yellow polyimide tube was not removed during manufacturing.
Product
FIBERNET Embolic Protection System: Recommended Vessel Diameter 5.0 -6.0 mm, Maximum Guidewire Diameter: 0.014 in (0.36mm) Rx only, Sterile; Manufactured in: Invatec S.P.A., Italy; Manufacturer: Medtronic Inc. Minneapolis, MN. The FiberNet Embolic Protection System is…
Category
Medical Device
Distribution
6 states
HighFDA (Food)·F-1688-2014·2014-04-02
Plum Baby Food Recalled for Potential Choking Hazard from Plastic Spout Damage
Plum Inc. is recalling specific varieties of Stage 2 World Baby food due to intermittent plastic spout damage that may cause choking.
Product
Stage 2 World Baby ; Zucchini & Spinach with Pasta Marinara; 3.5 oz. pouch. Product of USA distributed by Plum Inc., Emeryville, CA
Category
Food
Distribution
0 states
HighFDA (Devices)·Z-1306-2014·2014-04-02
Abbott i-STAT G3+ Cartridge Recall for Inaccurate Blood Gas Results
Abbott Point of Care is recalling i-STAT G3+ Cartridges (Lot N13183) because they may produce incorrectly elevated PCO2 and depressed pH results.
Product
i-STAT G3+ Cartridge pH, pCO2 and pO2 measurements are used in the diagnosis, monitoring and treatment of respiratory disturbances and metabolic and respiratory based acid-based disturbances.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1290-2014·2014-04-02
Teleflex Medical Recalls Weck Vista Universal Balloon Open Access Ports
Teleflex Medical is recalling 55,521 Weck Vista Universal Balloon Open Access Ports due to gas leakage that may delay laparoscopic surgeries.
Product
5/10/12 Weck¿ Vista" Universal Balloon Open Access Port Long Length (100mm), Product Usage: An endoscope and accessories is a device used to provide access, illumination, and allow observation or manipulation of body cavities, hollow organs, and canals.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1274-2014·2014-04-02
Synthes Ulna Osteotomy System Drill Template and Saw Guide Recall
Synthes, Inc. is recalling 343 Drill Templates and Saw Guides for the Ulna Osteotomy System due to potential mechanical failure of connecting screws or K-wires.
Product
Drill Template and the Saw Guide for the Ulna Osteotomy System. Intended for fixation of fractures, osteotomies, nonunions, replantations, and fusions of small bones and small bone fragments, including osteopenic bone in the ulna.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1305-2014·2014-04-02
Medtronic Recalls FiberNet Embolic Protection System Due to Manufacturing Defect
Medtronic is recalling specific lots of the FiberNet Embolic Protection System because a yellow polyimide tube was not removed during manufacturing.
Product
FIBERNET Embolic Protection System: Recommended Vessel Diameter 6.0 -7.0 mm, Maximum Guidewire Diameter: 0.014 in (0.36mm) Rx only, Sterile; Manufactured in: Invatec S.P.A., Italy; Manufacturer: Medtronic Inc. Minneapolis, MN. The FiberNet Embolic Protection System is…
Category
Medical Device
Distribution
6 states
HighFDA (Food)·F-1690-2014·2014-04-02
HP Hood Recalls my essentials Sour Cream Due to Metal Bolt Fragment
HP Hood LLC is recalling my essentials brand sour cream because a metal bolt fragment from a filling machine was found in the product.
Product
my essentials brand sour cream, NET WT. 24 OZ. (680g), UPC 7 25439 10546 0 --- Firm on label: DISTRIBUTED BY DZA BRANDS, LLC 2110 Executive Drive, Salisbury, NC 28147 --- The sour cream is packed in a plastic container.
Category
Food
Distribution
6 states
HighFDA (Food)·F-1684-2014·2014-04-02
Fairway Grilling Sauce Recalled for Undeclared Fish Allergen
Wolfgang B. Gourmet Foods is recalling Fairway brand Condiment Grilling Sauce because it contains undeclared fish (anchovies). The product was distributed in New York, New Jersey, and Connecticut.
Product
FAIRWAY brand CONDIMENT GRILLING SAUCE, NET WT 12 oz (340 g), UPC 7 58940 70609 3 -- Distributed By: Fairway Group Central Services LLC New York, New York 10027 --- The product is packaged in a glass bottle, 12 bottles per case.
Category
Food
Distribution
3 states
HighFDA (Devices)·Z-1202-2014·2014-04-02
Siemens Artis Q X-ray Systems Recalled for Potential Tube Breakdown
Siemens is recalling 19 Artis Q and Artis Q biplane systems because a breakdown of the x-ray tube could result in loss of x-ray imaging during clinical operation.
Product
Siemens Artis Q and Artis Q biplane systems Product Usage: Interventional Fluoroscopic X-ray
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1179-2014·2014-04-02
Hill Dermaceuticals Recalls Subpotent Fluocinolone Acetonide Topical Oil
Hill Dermaceuticals is recalling 4,142 bottles of Fluocinolone acetonide 0.01% Topical Oil because the active ingredient was found to be subpotent during routine testing.
Product
SETON PHARMACEUTICALS Fluocinolone acetonide 0.01% Topical Oil (Scalp Oil), 4 fl.oz., Rx only Manufactured by: Hill Dermaceuticals, Inc. For: Seton Pharmaceuticals NDC 13925-507-04
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1299-2014·2014-04-02
Bio-Rad D-10 Hemoglobin Testing System Software Recall
Bio-Rad is recalling D-10 Hemoglobin Testing Systems because the software may occasionally generate duplicate results with incorrect sample identifiers.
Product
D-10" Hemoglobin Testing System, Model number: 220-0220 Manufactured by: Bio-Rad Laboratories, Inc. 4000 Alfred Nobel Drive Hercules, CA 94545 The D-10 Hemoglobin Testing System is a single module designed for hemoglobin analysis in mid-volume laboratories. The D-10…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1181-2014·2014-04-02
Hill Dermaceuticals Recalls Subpotent Fluocinolone Acetonide Ear Drops
Hill Dermaceuticals is recalling 13,591 bottles of Fluocinolone Acetonide 0.01% Oil Ear Drops because routine testing found the active ingredient to be subpotent.
Product
SETON PHARMACEUTICALS Fluocinolone Acetonide 0.01% Oil EAR DROPS, 20 ml, Rx only Manufactured by: Hill Dermaceuticals, Inc. For: Seton Pharmaceuticals NDC 13925-508-20
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1692-2014·2014-04-02
Bonduelle Recalls Bulk Frozen Green Beans Due to Filth Presence
Bonduelle USA Inc is recalling bulk totes of frozen green beans due to the presence of filth. The product was distributed in Arkansas and Iowa.
Product
Bonduelle USA Inc (Oakfield) BEANS GREEN WHOLE GRADED, Net weight: 1,100 lbs (bulk form in Totes), Keep frozen.
Category
Food
Distribution
2 states
ModerateFDA (Food)·F-1697-2014·2014-04-02
New Horizon Cuisine Chicken Demi-Glace Recalled Due to Spoiled Chicken
New Horizon Cuisine is recalling Chicken Demi-Glace products because they were manufactured using chicken reported to be spoiled by another government agency.
Product
New Horizon Cuisine Chicken Demi-Glace Xpress, packaged in 16-oz. plastic cups (6/case) and New Horizon Cuisine Chicken Demi-Glace packaged in 16-lb. (2-gal.) buckets. The firm name on the label is New Horizon Cuisine, Ankeny, IA.
Category
Food
Distribution
3 states
ModerateFDA (Devices)·Z-1300-2014·2014-04-02
Bard Access Systems Recalls PowerPort Slim Implantable Ports Due to Labeling Error
Bard Access Systems is recalling 777 PowerPort Slim Implantable Ports because the labels incorrectly state they contain silicone suture plugs, when some units do not.
Product
PowerPort Slim Implantable Port, indicated for patient therapies requiring repeated access to the vascular system. Product Codes: 1716000, 1716070
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1273-2014·2014-04-02
Spacelabs Recalls G2 Clinical Access Software CDs Due to Incorrect Programs
Spacelabs Healthcare is voluntarily recalling G2 Clinical Access Software CDs because they contain incorrect programs, preventing customers from installing the software.
Product
Spacelabs Healthcare G2 Clinical Access Mislabeled CDs for PN: 063-1829-11 Rev A and Update Kit, PN: 040-1565-10. Used for installing ICS G2 Clinical Access software onto hospital personal computers.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1268-2014·2014-04-02
AMS Uric Acid Test Kits Recalled for Regulatory Violations
AMS Diagnostics is recalling 13 Uric Acid test kits because they were marketed outside FDA 510(k) requirements.
Product
AMS URIC ACID For the In vitro quantitative determination of Uric Acid in serum Quantitative determination of Uric Acid in serum.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1269-2014·2014-04-02
AMS AST Diagnostic Kits Recalled for Marketing Outside 510(k) Requirements
AMS Diagnostics is recalling 116 AMS AST kits because they were marketed outside FDA 510(k) requirements. The recall covers nationwide distribution.
Product
AMS AST For the In vitro quantitative determination of AST in serum Quantitative determination of AST in serum.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1178-2014·2014-04-02
Hill Dermaceuticals Recalls Subpotent Dermotic Ear Drops
Hill Dermaceuticals is recalling Dermotic ear drops because the active ingredient was found to be subpotent during routine testing.
Product
DERMOTIC — DERMOTIC (FLUOCINOLONE ACETONIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1180-2014·2014-04-02
Hill Dermaceuticals Recalls Subpotent Fluocinolone Acetonide Topical Oil
Hill Dermaceuticals is recalling 7,676 bottles of Fluocinolone Acetonide 0.01% Topical Oil because the active ingredient was found to be subpotent during routine testing.
Product
SETON PHARMACEUTICALS Fluocinolone Acetonide 0.01% Topical Oil (Body Oil), 4 fl.oz., Rx only Manufactured by: Hill Dermaceuticals, Inc. For: Seton Pharmaceuticals NDC 13925-506-04
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1176-2014·2014-04-02
Hill Dermaceuticals Recalls Subpotent Fluocinolone Acetonide Topical Oil
Hill Dermaceuticals is recalling 8,734 bottles of Derma-Smoothe/FS topical oil because the active ingredient was found to be subpotent during routine testing.
Product
DERMA-SMOOTHE/FS — DERMA-SMOOTHE/FS (FLUOCINOLONE ACETONIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1267-2014·2014-04-02
AMS BUN Urea Nitrogen Kits Recalled for Marketing Violations
AMS Diagnostics is recalling 167 BUN Urea Nitrogen kits because they were marketed outside FDA 510(k) requirements.
Product
AMS BUN UREA NITROGEN For the In vitro quantitative determination of Urea Nitrogen in serum Quantitative determination of Bun in serum.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1175-2014·2014-04-02
Hill Dermaceuticals Recalls Subpotent Fluocinolone Acetonide Topical Oil
Hill Dermaceuticals is recalling 8,734 bottles of Derma-Smoothe/FS fluocinolone acetonide 0.01% Topical Oil because the active ingredient was found to be subpotent during routine testing.
Product
Derma-Smoothe/FS fluocinolone acetonide 0.01% Topical Oil (Body Oil) 4 fl. oz., Rx only Manufactured and Distributed by: Hill Dermaceuticals, Inc. Sanford, Florida 32773 NDC 28105-150-04
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1686-2014·2014-04-02
Mars Food US Recalls Uncle Ben's Ready Rice Due to Package Punctures
Mars Food US is voluntarily recalling Uncle Ben's Ready Rice because package punctures caused spoilage. Consumers should check for damaged packaging.
Product
UNCLE BEN's(R) READY RICE(R) Original Enriched Long Grain White Rice, 8.8 oz. (250g), UPC 054800 031764
Category
Food
Distribution
20 states
LowFDA (Drugs)·D-1173-2014·2014-04-02
Hill Dermaceuticals Recalls Subpotent DermOtic Oil Ear Drops
Hill Dermaceuticals is recalling DermOtic Oil ear drops because the active ingredient was found to be subpotent during routine testing.
Product
DermOtic Oil (fluocinolone acetonide) 0.01% Ear Drops, 20 mL bottle, Rx only Manufactured and Distributed by: Hill Dermaceuticals, Inc. Sanford, Florida 32773 NDC 28105-160-20
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1174-2014·2014-04-02
Hill Dermaceuticals Recalls Subpotent Fluocinolone Acetonide Topical Oil
Hill Dermaceuticals is recalling 14,226 bottles of Derma-Smoothe/FS fluocinolone acetonide 0.01% Topical Oil because the active ingredient was found to be subpotent during routine testing.
Product
Derma-Smoothe/FS fluocinolone acetonide 0.01% Topical Oil (Scalp Oil), 4 fl. oz., Rx only. Manufactured and Distributed by: Hill Dermaceuticals, Inc. Sanford, Florida 32773 NDC 28105-149-04
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1270-2014·2014-04-02
Lin-Zhi Norbuprenorphine Calibrator Recalled for Quality Control Failure
Lin-Zhi International is recalling Norbuprenorphine cutoff calibrators because they failed quality control testing. The product is used for in vitro diagnostic calibration.
Product
Single Analyte DAU Calibrator (5 mL) Norbuprenorphine: Cutoff Calibrator; IVD - for in vitro diagnostic use only; Lin-Zhi International Sunnyvale, CA The Norbuprenorphine Drug of Abuse (DAU) cutoff Calibrator is used for qualitative and semi-qualitative calibration of the…
Category
Medical Device
Distribution
1 state
LowFDA (Devices)·Z-1297-2014·2014-04-02
TriVascular Ovation Prime Abdominal Stent Graft System Instructions for Use Update
TriVascular, Inc. is notifying European physician users of the Ovation Prime Abdominal Stent Graft System about changes to the Instructions for Use.
Product
Ovation Prime Abdominal Stent Graft System; Manufacturer: TriVascular, Inc. 3910 Brickway Blvd. Santa Rosa, CA 95403 The TriVascular Ovation Prime Abdominal Stent Graft System is an endovascular device delivered via a small diameter catheter to treat abdominal aortic…
Category
Medical Device
Distribution
0 states
LowFDA (Food)·F-1691-2014·2014-04-02
Bonduelle Recalls Bulk Frozen Green Beans Due to Filth Presence
Bonduelle USA Inc is recalling bulk totes of frozen cut and whole green beans due to the presence of filth.
Product
Bonduelle USA Inc (Oakfield) BEANS GREEN CUT GRADED, Net weight: 1,480 lbs (bulk form in Totes), Keep frozen.
Category
Food
Distribution
2 states
LowFDA (Drugs)·D-1177-2014·2014-04-02
Hill Dermaceuticals Recalls Subpotent Fluocinolone Acetonide Scalp Oil
Hill Dermaceuticals is recalling 7,292 bottles of Derma-Smoothe/FS scalp oil because the active ingredient was found to be subpotent during routine testing.
Product
DERMA-SMOOTHE/FS — DERMA-SMOOTHE/FS (FLUOCINOLONE ACETONIDE)
Category
Drug
Distribution
Distributed nationwide
SevereUSDA FSIS·019-2014·2014-04-01
AdvancePierre Recalls Frozen Chicken Fritters Due to Undeclared Allergens
AdvancePierre Foods is recalling frozen chicken breast fritters because they contain undeclared milk and soy. The products were distributed to food service establishments in 15 states.
Product
AdvancePierre Foods, Inc. — Oklahoma Firm Recalls Chicken Products Due To Misbranding and Undeclared Allergens
Category
Food
Distribution
15 states
SevereNHTSA·14V161000·2014-04-01
Chrysler Recalls 2014 Ram 1500 4x4 Trucks for Transmission Defect
Chrysler is recalling 125 model year 2014 Ram 1500 4x4 vehicles because the transmission case may be improperly machined, preventing the park pawl from engaging and increasing the risk of a crash.
Product
RAM — RAM 1500
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·14E012000·2014-04-01
Ohlins Recalls Steering Damper Kits for Cracking Bracket Risk
Ohlins Racing AB is recalling steering damper kits for various motorcycles because an incorrectly machined bracket may crack, potentially causing steering to lock at low speeds.
Product
DUCATI — DUCATI, HONDA, YAMAHA 848, 916, 748, CBR600RR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·14V154000·2014-04-01
Chrysler Recalls 2011-2014 Jeep Grand Cherokee and Dodge Durango for Brake Booster Defect
Chrysler is recalling 2011-2014 Jeep Grand Cherokee and Dodge Durango vehicles because a corroding brake booster may allow water to enter, potentially freezing and limiting braking ability.
Product
JEEP — JEEP, DODGE GRAND CHEROKEE, DURANGO
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·14C002000·2014-04-01
Baby Trend Recalls 2011-2012 TrendZ Fastback Child Restraints for Buckle Defect
Baby Trend is recalling 2011 and 2012 TrendZ Fastback 3-in-1 child restraints because the harness buckle may become stuck, making it difficult to remove a child in an emergency.
Product
CHILD SEAT:HARNESS/CROTCH BUCKLE recall
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·14143·2014-04-01
Dyson Recalls Bladeless Portable Electric Heaters Due to Fire Hazard
Dyson is recalling about 338,000 portable electric heaters in the U.S. because they can short-circuit and overheat, posing a fire hazard.
Product
Portable electric heaters
Category
Consumer Product
Distribution
Distributed nationwide

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