KEEP YOUR KIDS SAFE-MARCH 2019 RECALLS
FOR ANTIGO TIMES
Release Number: (#19-058) Fisher-Price, of East Aurora, N.Y., is announcing the voluntary recall of about 44,000 children’s power wheels Barbie Dream Campers. This recall involves children’s Power Wheels Barbie Dream Campers with model number FRC29 with a grey foot pedal. The recalled ride-on vehicles are hot pink with blue accents and have the Barbie logo printed on the back. They are battery-operated and have a play kitchen, a fold out grill and pretend campfire. The model number is printed on a label under the hood.
Problem: The children’s ride-on Power Wheels can continue to run after the foot pedal is released, posing an injury hazard.
What to do: Consumers should immediately take the recalled Power Wheels away from children, stop using them and contact FisherPrice for a free repair. Consumers can contact Fisher-Price at 800-348-0751 from 9 a.m. to 6 p.m. ET Monday through Friday or online at www.service.mattel.com and click on “Recalls & Safety Alerts” or www.fisher-price.com and click on “Recalls” for more information.
https://www.cpsc.gov/Recalls/2019/Fisher‐Price‐ Recalls‐Childrens‐Power‐Wheels‐Barbie‐Campers‐ Due‐to‐Injury‐Hazard#
Release Number: (#19-062) Target Corp., of Minneapolis, Minn., is announcing the voluntary recall of about 33,600 Cat & Jack Unicorn “Chiara” Boots. This recall includes the Cat & Jack “Chiara” toddlers’ unicorn boots in sizes 5- 13, and size 1. The boots are white with silver shimmer, include a white zipper, and white faux fur lining. The unicorn’s horn and inner ears are silver glitter and its eyelashes and nostrils are stitched and gray in color. At the base of the unicorn’s horn is pink, purple, and blue faux fur. The back and sides of the boots contain multi-colored stripes. The model numbers are located on the inside tag of the boot. The recalled model numbers begin with TARGET0930156XX, where XX corresponds to a specific sized boot.
Problem: The unicorn horn on the boot can detach, posing a choking hazard to children.
What to do: Consumers should immediately take the recalled boots away from children and return them to any Target Store for a full refund. Consumers can contact Target at 800-440-0680 from 7 a.m. to 8 p.m. CT, daily or online at www.target.com and click on “Recalls” at the bottom of the page, then on “Clothing” for more information. Consumers can also click the “Product Recalls” tab on Target’s Facebook page for more information.
Release Number: (#19-068) Crate and Barrel of Northbrook, Ill., is announcing the voluntary recall of about 17,000 Crate and Barrel holiday bear acrylic milk bottles. This recall involves Crate and Barrel’s Holiday Bear Acrylic Milk Bottle. The clear acrylic bottle measures 5.5 inches tall and 2.75 inches wide at the base and has a removable plastic straw. A graphic of a bear in a red sweater is printed on the wide part of the bottle.
Problem: The plastic straw that comes with the milk bottle can crack or break, posing a laceration hazard.
What to do: Consumers should immediately stop using the recalled milk bottles and contact Crate and Barrel to receive a full refund. Consumers can contact Crate and Barrel at 800- 451-8217 from 8 a.m. to 8 p.m. CT Monday through Friday and 8 a.m. to 7 p.m. CT Saturday through Sunday or online at www.crateandbarrel.com and click on “Product Recall” for more information.
Release Number: (#19-069) SRAM LLC, of Chicago, Ill., is announcing the voluntary recall of about 7,000 SPRAM i-Motion 3 internal gear hubs (coaster brake version) for bicycles. This recall involves SRAM® i-Motion 3 three-speed internal gear hubs with a coaster brake installed on bicycles with no redundant braking system. The recalled hubs were sold on the following Electra® model bicycles: Electra Cruiser Custom 3i, Electra Coaster 3i, Electra Hawaii 3i, Electra Hawaii 3i 24 and Electra Straight 8. The recalled hubs were also sold as aftermarket parts for other bicycles. The recalled hubs have “SRAM iMotion 3” printed on the hub shell and a brake arm extending from the axle of the hub.
Problem: The brakes in the gear hubs can fail, posing crash and injury hazards to the rider.
What to do: Consumers should immediately stop using bicycles with the recalled gear hubs and contact SRAM for instructions on how to receive a partial refund. Consumers can contact SRAM at 800-346-2928 from 10 a.m. to 7 p.m. ET Monday through Thursday and 10 a.m. to 6 p.m. ET on Friday or online at www.sram.com or www.zipp.com and click on “Recall Notice” for more information.
Release Number: (#19-071) JumpSport Inc., of Campbell, Calif., is announcing the voluntary recall of about 11,300 JumpSport® half-fold fitness mini-trampolines. This recall involves folding JumpSport mini trampolines. The recalled fitness trampoline models have a hinged, round metal frame with a black fabric jumping surface suspended by bungee cords. Some models were sold with accessories, such as a handlebar or workout videos. The model number is printed on a label on the upper portion of one of the trampoline legs. “JumpSport” and “Fitness Trampoline” are printed on the black fabric jumping surface.
Problem: The folding trampoline’s frame can forcefully hit the user, posing an injury hazard.
What to do: Consumers should immediately stop using the recalled trampolines and visit JumpSport’s website to DOWNLOAD a new instructional manual and warning materials. If the trampoline is set up, consumers should not try to fold it until they have reviewed the new instructions and warnings. New instructions are also available directly from JumpSport. Consumers can contact JumpSport toll-free at 855-782-9980 from 9 a.m. to 6 p.m. ET Monday through Friday, email at [email protected] or online at www.jumpsport.com and click on “Recalls” for more information or to request a copy by mail.
Release Number: (#19-072) D&D Futon Furniture, of South El Monte, Calif., is announcing the voluntary recall of about 800 sleeper chair folding foam beds. This recall involves the gray D&D Futon Furniture Sleeper Chair Folding Foam Bed which can be used as a chair or bed and were sold in 24, 32, 36, and 48 inches wide sizes. The sleeper chair is 6 inches high when configured as a mattress.
Problem: The mattress fails to meet the mandatory federal flammability standard for mattresses, posing a fire hazard.
What to do: Consumers should immediately stop using the recalled mattresses and contact D&D Futon Furniture to receive a free fitted liner to cover the mattress and bring it into compliance with the federal standard. Consumers can contact D&D Futon Furniture toll-free at 877-416-5226 from 9:30 a.m. to 5 p.m. PTMonday through Friday at [email protected] or online at www.ddfutonfurniture.com and click on Recall for more information.
Release Number: (#19-075) Biotouch Inc., of City of Industry, Calif., is announcing the voluntary recall of about 8,500 EZY gel topical anesthetic gel. This recall involves EZY Gel Topical Anesthetic Gel. The recalled product was sold in 1 fluid ounce white bottles. Biotouch Topical Anesthetic Gel EZY Gel is printed on a purple label located on the front panel. Lot numbers and expiration dates are located on the bottom of the bottle.
Problem: The package is not child resistant as required by the Poison Prevention Packaging Act. The pain relieving gel contains lidocaine, posing a risk of poisoning to young children.
What to do: Consumers should immediately place the recalled topical anesthetic out of reach of children and contact Biotouch for instructions on how to obtain a full refund, including shipping. Consumers can contact Biotouch tollfree at 844-557-9023 from 10 a.m. to 4 p.m. PT Monday through Friday, email at [email protected] , or online at www.biotouch.com and click on Recall at the bottom of the page for more information.
Release Number: (#19-076) Clinical Resolution Laboratory, Inc. of Brea, Calif., is announcing the voluntary recall of about 26,500 Numb 100 topical anesthetic cream. This recall involves Numb 100 Topical Anesthetic Cream. The recalled cream is in a 1.35 fluid ounce white jar with a rounded cap. Numb 100 Topical Anesthetic Cream and a blue cross are printed on the jar’s front panel.
Problem: The packaging is not child resistant as required by the Poison Prevention Packaging Act. The pain relieving cream contains lidocaine, posing a risk of poisoning to young children if they put it on their skin or ingest it.
What to do: Consumers should immediately place the recalled topical anesthetic out of reach of children and contact Clinical Resolution Laboratory for a full refund, a free replacement cream, or free replacement child-resistant cap. Consumers can contact Clinical Resolution Laboratory toll-free at 877-566-9687 from 8 a.m. to 5 p.m. PT Monday to Friday, email at [email protected] or online at www.clinicalresolution.com and click on the Recall Information tab at the top of the page for more information.