Author: jbushland

Name of product:
DaVinci Bailey bassinets
Hazard:

The bassinet’s support legs can break, posing a fall hazard to babies.

Remedy:
Repair
Recall date:
December 5, 2019
Units:
About 3,000 (In addition, about 290 in Canada)
Consumer Contact:

DaVinci toll-free at 833-932-0208 Monday through Friday from 9 a.m. to 5 p.m. PT, email at bailey@milliondollarbaby.zendesk.com or online at www.davincibaby.com/baileyrepair or www.davincibaby.com and click on “Recalls” under the Help tab for more information.

Recall Details

In Conjunction With:
Description:

This recall involves wooden DaVinci Bailey Bassinets for infants. The recalled bassinets were sold in the following four colors, with corresponding product numbers – gray (M0934G), espresso (M0934Q), natural (M0934N) and white (M0934W). The model number “0934” is printed on a white label attached to the mattress support board and on the external product package. The assembled bassinets measure 38 inches long by 20 inches wide by 30 inches high, and each weighs about 21 pounds. The bassinets were sold with a 1-inch waterproof cradle pad. “DaVinci” is printed on the product packaging, instruction manual and product registration card.

Remedy:

Consumers should immediately stop using the recalled bassinets and contact DaVinci for a free repair kit that includes new support legs. In the meantime, parents are urged to remove the support legs and use the bassinet on a safe space on the floor or to find an alternate, safe sleeping environment for the child, such as a crib that meets current safety standards. DaVinci is contacting all known purchasers directly.

Incidents/Injuries:

DaVinci has received 19 reports of the bassinet legs breaking. No injuries have been reported. (more…)

Class II Recall118-2019
Health Risk: LowNov 29, 2019

Congressional and Public Affairs
Emmanuel Olufotebi
(202) 720-9113
FSISpress@usda.gov

 

WASHINGTON, Nov. 29, 2019 – Blue Grass Quality Meats, an Erlanger, Ky. establishment, is recalling approximately 121,083 pounds of pork bacon and ready-to-eat turkey products due to misbranding and undeclared allergens, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The products contain soy, a known allergen, which is not declared on the product labels.

The Cajun style bacon and ready-to-eat Cajun style turkey breast items were produced on various dates from Oct. 29, 2018 to Nov. 19, 2019. The following products are subject to recall: [View Labels (PDF only)]

  • Various weights of shrink-wrap packages containing “BLUE GRASS CAJUN STYLE TURKEY BREAST” with sell by dates from 7/1/19 to 1/9/20.
  • Various weights of shrink-wrap packages containing “OLDE WORLD Cajun Style TURKEY BREAST” with sell by dates from 7/1/19 to 1/1/20.
  • Various weights of shrink-wrap packages containing “Robinson’s PREMIUM Cajun Style Turkey Breast” with sell by dates from 7/12/19 to 1/16/20.
  • Various weights of shrink-wrap packages containing “Troyer CAJUN STYLE TURKEY BREAST” with sell by dates from 7/18/19 to 1/21/20.
  • Various weights of vacuum sealed packages containing “Troyer CAJUN STYLE BACON” with sell by dates from 1/28/19 to 2/19/20.

The products subject to recall bear establishment number “P-7417” or “EST. 7417” inside the USDA mark of inspection. These items were shipped to retail locations in Kentucky, Michigan, Ohio and West Virginia, where the turkey products may have been offered as retail-sliced deli product.

The problem was discovered when the firm’s seasoning supplier notified them that the proprietary seasoning, which is not supposed to contain soy, actually contains soy lecithin.

There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.

(more…)

Summary

Company Announcement Date:
November 27, 2019
FDA Publish Date:
November 27, 2019
Product Type:
Food & Beverages
Reason for Announcement:
Potential E.coli Contamination
Company Name:
UNFI
Brand Name:
Wild Harvest
Product Description:
Organic All-Purpose Flour

Company Announcement

UNFI announced today a voluntary national recall of five-pound bags of its Wild Harvest® Organic All-Purpose Flour, Unbleached, with a Code of AA BEST IF USED BY 010820 CC 15:58 and UPC Code 711535509158. The recall is being issued for the potential presence of E. coli. During routine FDA sampling of the five-pound bag product, results were found to be positive for E.coli.

E. coli can cause serious and sometimes life-threatening infections in infants, older people, pregnant women, and people with weakened immune systems. The most common symptoms of E. coli are diarrhea, abdominal cramps, nausea and vomiting, which develop within three or four days of eating contaminated food. The illness usually lasts about a week and most people recover without treatment. Guidance from FDA and the Centers for Disease Control (CDC) continues to warn that consumers should refrain from consuming any raw products made with flour and that all surfaces, hands and utensils should be properly cleaned after contact with flour or dough.

To date, UNFI has not received any direct consumer reports of confirmed illnesses related to this product. This recall is being issued out of an abundance of care. (more…)

Summary

Company Announcement Date:
November 27, 2019
FDA Publish Date:
November 27, 2019
Product Type:
Food & Beverages
Reason for Announcement:
Potential E. Coli Contamination
Company Name:
Hodgson Mill, Inc.
Brand Name:
Hodgson Mill
Product Description:
Unbleached Flour

Company Announcement

Hodgson Mill of Effingham, IL, announced today a voluntary national recall of specific lots of its Unbleached All-Purpose White Wheat Flour (5 lb.)

We are taking this voluntary precautionary step because of the potential presence of pathogenic E. coli which was discovered through sampling raw uncooked flour. Hodgson Mill has not received any confirmed reports of illnesses related to this product. (more…)

Summary

Company Announcement Date:
November 27, 2019
FDA Publish Date:
November 27, 2019
Product Type:
Food & Beverages
Reason for Announcement:
Potential Listeria monocytogenes Contamination
Company Name:
Fuji Food Products, Inc.
Brand Name:
Okami & Trader Joes
Product Description:
Ready to eat sushi, salads and spring rolls

Company Announcement

Fuji Food Products, Inc. (Fuji) announced today the voluntary recall of ready to eat sushi, salads and spring rolls sold to select retailers and distributors along the East Coast and Upper Midwest. The voluntary recall is in response to a notification by the Food and Drug Administration (FDA) of the potential for product contamination with Listeria monocytogenes. To date, public health officials have not reported any illness associated with these products. (more…)

Name of product:
Stacked Gourd Jack-O-Lantern decorations
Hazard:

The string light wiring inside of the Jack-O-Lanterns can overheat, spark or ignite, posing a fire hazard.

Remedy:
Refund
Recall date:
November 26, 2019
Units:
About 5,000
Consumer Contact:

Mark Feldstein & Associates at 800-755-6504 from 8:15 a.m. to 5 p.m. ET Monday through Friday, email at Sales@MFAgifts.com or visit www.MFAgifts.com and click on the Recall Information button on the homepage for more information.

Recall Details

Description:

This recall involves Stacked Gourd Jack-O-Lantern decorations. The 12-inch Jack-O-Lantern is hand-painted resin and has battery-operated LED string lights inside the product. The Jack-O-Lantern’s lights are powered with three AAA batteries. Printed on a hang tag and a label on the box is UPC code 789683062481, model number S1915D12 and Mark Feldstein & Associates Inc.

Remedy:

Consumers should immediately stop using the recalled Stacked Gourd Jack-O-Lantern decorations and contact Mark Feldstein & Associates to receive a full refund

Incidents/Injuries:

The firm has received four reports of the Jack-O-Lantern decorations smoking or catching on fire.  No injuries or property damage have been reported. (more…)

Name of product:
19 different recalled products
Hazard:

Hazards include infant fatalities, fire, burn, choking, fall, laceration, skin irritation, explosion or other injuries depending on the product.

Remedy:
Refund
Replace
Repair
Recall date:
November 26, 2019
Units:
About 1,200
Consumer Contact:

Contact directly the recalling companies listed below in the “Recall Details” section of this press release for the remedy. T.J. Maxx, Marshalls, and HomeGoods can be reached as follows:

T.J. Maxx at 800-926-6299 from 9 a.m. to 6 p.m. ET Monday through Friday or online at www.tjmaxx.com then click on Contact Us at the bottom of the page.

Marshalls at 888-627-7425 from 9 a.m. to 6 p.m. ET Monday through Friday or online at www.marshalls.com and click on Contact Us at the bottom of the page.

HomeGoods at 800-888-0776 from 9 a.m. to 6 p.m. ET Monday through Friday or online at www.homegoods.com and click on Customer Service at the bottom of the page.

Recall Details

Description:

The U.S. Consumer Product Safety Commission (CPSC) and The TJX Companies Inc. are warning consumers that T.J. Maxx, Marshalls and HomeGoods sold 19 different recalled products after they were recalled between 2014 and 2019. This involves about 1,200 units of recalled products sold to consumers. Consumers should stop using the recalled products immediately and contact the recalling firms to receive the remedy listed in the recall, which is either a refund, replacement or repair. (more…)

Name of product:
2018 and 2019 Yamaha EF2000iS portable generators
Hazard:

The portable generator’s fuel tank can leak gasoline, posing fire and burn hazards.

Remedy:
Repair
Recall date:
November 26, 2019
Units:
About 10,100
Consumer Contact:

Consumer Contact: Yamaha toll-free at 866-788-7398 anytime or online at www.yamahamotorsports.com or www.yamahamotorsports.com/power-product and click on the CPSC Alerts tab at the bottom of the page for more information.

Recall Details

Description:

This recall involves model 2018 and 2019 Yamaha EF2000iS portable generators, with serial numbers range 4543288 through 4553706. The blue generators have Yamaha and the model name printed on the control panel. The serial number can be found on a label below the exhaust outlet on the left side.

Remedy:

Consumers should immediately stop using the recalled generators and contact a Yamaha Power Products dealer to schedule a free repair. Yamaha is contacting all registered owners directly.

Incidents/Injuries:

None reported (more…)

Name of product:
STANLEY® brand 16 oz. wooden handle nailing hammer
Hazard:

The molded grip on the hammer can come loose, posing an injury hazard to consumers.

Remedy:
Refund
Recall date:
November 27, 2019
Units:
About 211,000
Consumer Contact:

Stanley toll-free at 866-215-1132 from 8 a.m. to 5 p.m. ET Monday through Friday, email recall@sbdinc.com or online at www.stanleytools.com click on Support then Safety Notices and Recalls for more information.

Recall Details

Description:

This recall involves the STANLEY brand 16 oz. wooden handle nailing hammers with model number STHT51454 etched below the STANLEY logo on the steel hammer head. The hammers have a metal head, a natural wood handle with a black over- molded grip. STANLEY is marked on the wooden handle in black and on the steel hammer head. The UPC code for the product is 076174514544 and is located on a label on the handle.

Remedy:

Consumers should immediately stop using the recalled hammers and return them to Walmart to receive a refund in the form of a Walmart gift card for the purchase price.

Incidents/Injuries:

Stanley Black & Decker has received one report of the hammer’s grip coming loose. No injuries have been reported. (more…)

Summary

Company Announcement Date:
November 15, 2019
FDA Publish Date:
November 26, 2019
Product Type:
Medical Devices
Reason for Announcement:
Potential leakage at joint between blood filter and tubing
Company Name:
B. Braun Medical, Inc.
Brand Name:
B. Braun
Product Description:
Blood Administration Kits

Company Announcement

B. Braun Medical Inc. [B. Braun] initiated a voluntary recall of twenty-two (22) lots of Blood Administration Sets. The recalled blood administration sets are used to administer blood from a container to a patient’s vascular system through an IV catheter inserted into a vein or central venous catheter.

B. Braun identified through complaints and internal discrepancies the potential for leakage at the joint between the blood filters and tubing of these blood administration sets. Blood set leakage may result in delay in therapy due to the need to replace the set and blood product or result in the potential for microorganisms to enter the circulatory system creating a risk of bloodstream infection. To date there have been no reports of serious injury or death. (more…)