Baby and kids' product recalls
6681 federal recalls on file. Every federal recall touching baby and kids' products — toys, formula, baby food, cribs, strollers, child seats. Sourced from CPSC, FDA, USDA, and NHTSA, translated into plain English.
- 2012-10-18CPSCDream On Me Inc., of South Plainfield, N.J.Dream On Me Recalls Infant Swings Due to Strangulation Hazard
The opening between the tray and seat or the grab bar and seat can allow a child's body to pass through and become entrapped at the neck, posing a strangulation hazard to young children if the belt is not engaged.
- 2012-10-18CPSCDream On Me Inc., of South Plainfield, N.J.Dream On Me Recalls High Chairs Due to Strangulation Hazard
The front openings between the tray and seat bottom and on the side openings of the high chair between the armrest and seat bottom can allow a child's body to pass through and become entrapped at the neck. This poses a strangulation hazard to young children if the belt is not engaged. In addition, exposed springs between the seat and armrest on both sides of the high chair can create a pinch hazard to the child.
- 2012-10-18CPSCTrend Lab LLC, of Burnsville, Minn.Trend Lab Recalls Children's Upholstered Chairs Due to Laceration and Choking Hazards
Staples in the binding on the back of the chair may come loose, posing a laceration or choking hazard if swallowed.
- 2012-10-17FDA-DeviceMedtronic Sofamor Danek USA IncClass IIPREMIER(R) Anterior Cervical Plate System SCREW BLOCK, REF 1860503, QTY: 1 EA, Rx only, Medtronic Sofamore Danek USA, Inc., 1800 Pyramid Place, Memphis, Tennessee 38132. Orthopedic. This instrument is a precision device which may incorporate a measuring function and has uses as described on the label. Unless labeled for single use, this instrument may be re-used.
Lines on the screw gauge may not placed on the caddy properly which could result in improper measurement of screws. An incorrect gauge could measure a screw to be approximately 1 mm shorter than its actual length.
- 2012-10-17FDA-DeviceMedtronic Sofamor Danek USA IncClass IIATLANTIS(R) Anterior Cervical Plate System FIXED ANGLE SCREW MODULE, REF 176-504, QTY: 1 EA, Rx only, Medtronic Sofamore Danek USA, Inc., 1800 Pyramid Place, Memphis, Tennessee 38132. Orthopedic. This instrument is a precision device which may incorporate a measuring function and has uses as described on the label. Unless labeled for single use, this instrument may be re-used.
Lines on the screw gauge may not placed on the caddy properly which could result in improper measurement of screws. An incorrect gauge could measure a screw to be approximately 1 mm shorter than its actual length.
- 2012-10-17FDA-DeviceMedtronic Sofamor Danek USA IncClass IIATLANTIS(R) Anterior Cervical Plate System VARIABLE ANGLE SCREW MODULE, REF 176-503, QTY: 1 EA, Rx only, Medtronic Sofamore Danek USA, Inc., 1800 Pyramid Place, Memphis, Tennessee 38132. Orthopedic. This instrument is a precision device which may incorporate a measuring function and has uses as described on the label. Unless labeled for single use, this instrument may be re-used.
Lines on the screw gauge may not placed on the caddy properly which could result in improper measurement of screws. An incorrect gauge could measure a screw to be approximately 1 mm shorter than its actual length.
- 2012-10-17FDA-FoodEco Health, Inc.Class IflorAlign Prebiotic Formula, sizes: 90g, 180g, 270g
Eco Health is recalling florAlign Prebiotic Formula because it has the potential to be contaminated with Salmonella.
- 2012-10-17FDA-FoodGM Distributing Co, IncClass IMarathon brand- 4 kilo boxes, label on the mango says "MARATHON...PRODUCE OF MEXICO", 952 ctns. of number 6 mangos, 714 ctns. of number 7's, 1186 ctns. of number 8's, 952 ctns. of number 9's, 714 ctns. of number 10's, 476 ctns. of number 12's.
GM Produce Sales is voluntarily recalling 4994 cartons of Marathon Brand mangos packed at Agricola Daniella, in Los Mochis, Sinaloa, because it has the potential to be contaminated with Salmonella gaminara, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella
- 2012-10-16CPSCChildren's Apparel Network, Ltd. of New York, N.Y.Children's Apparel Network Recalls Fleece Hoodie and T-Shirt Sets Due to Violation of Lead Paint Standard; Sold Exclusively at Target
The surface coating on the zipper of the fleece hoodie and t-shirt sets contain excessive levels of lead, violating the federal lead paint standard.
- 2012-10-10FDA-DeviceCure Medical LLCClass IIMale, 16Fr, Straight-tip Intermittent Urinary Catheters M16. The product is distributed individually or in intermediate boxes containing 30 individual, sterile packaged catheters (PA/PE film and dialyzing paper pouches). There are 30 catheters packaged in sterile pouches that are placed into an intermediate box, 10 of these intermediate boxes packaged into one case. K072539 The Cure Catheter" device, M16, is an intermittent urinary catheter intended to be used by males for the purpose of bla
The firm initiated the product recall because labeling on some of the intermediate boxes of catheters identify the contents to be M16C, a coud¿-tip catheters while the actual contents are M16Fr male, 16Fr, straight-tip catheters with the pouch and the case box labeled as M16Fr male, 16Fr, straight-tip catheters.
- 2012-10-09CPSCGraco Children's Products Inc., of Atlanta, GaGraco Recalls Classic Wood Highchairs Due to Fall Hazard
The high chair's seat can loosen or detach from the base, posing a fall hazard to the child.
- 2012-10-04CPSCFranshaw, Inc., of New York, N.Y.Pink Angel Embroidered Girls' Denim Shorts Recalled by Buy Buy Baby Due to Choking Hazard
Decorative studs on the denim shorts' pockets can detach and pose a choking hazard to young children.
- 2012-10-03FDA-DeviceRAYSEARCH LABORATORIES ABClass IISharePlan 1.1, aka t-RayAutoplan version 1.2.1 (build number 1.3.1.10). Manufacturing name RayAutoplan, aka t-RayAutoplan, commercial name (TomoTherapy) SharePlan Intended use: t-RayAutoplan is a software that, based on the planned dose distribution from a TomoPlan treatment planning system, generates a family of individually optimized IMRT plans and presents their characteristics to the user in a GUI. Among the generated plans, the user selects and clinically approves a treatment plan and e
This notice concerns behavior of the SharePlan that may be unexpected and not clearly described in the user manual. This behavior has not caused patient mistreatment or other incidents. However, the described user actions must be adhered to for best agreement between treatment plan evaluation and the clinical outcome of the delivered treatment. The behavior appears, when importing RFA-files (.asc)
- 2012-09-27NHTSA-EquipmentEvenflo Company, Inc.Evenflo Company, Inc. — Packaged Without Registration Card/FMVSS 213
Without the instruction manual the seat may be used improperly. Should the owner not file a registration with the child seat manufacturer due to lack of information on how to do so, they may not be notified of a safety recall. Either condition puts the child at an increased risk of possible injury in the event of a crash.
- 2012-09-27CPSCYCH Industries Corp., of TaiwanCyclone Swing Seats Recalled by ADS Due to Fall Hazard
The plastic swing seats can break during use, posing a fall hazard to children.
- 2012-09-26FDA-DeviceRAYSEARCH LABORATORIES ABClass IIThe product affected by this notice is sold under the trade name TomoTherapy SharePlan 1.1. To determine if the version you are using is affected, bring up the About box in the SharePlan application and check if the build number reported there is 1.3.1.10. Intended use: t-RayAutoplan is a software that, based on the planned dose distribution from a TomoPlan treatment planning system, generates a family of individually optimized IMRT plans and presents their characteristics to the user in
This field notice concerns two behaviors of the SharePlan (Multiple Fraction Groups and Depth Offset) that may be unexpected and are not clearly described in the user manual. None of these behaviors have caused patient mistreatment or other incidents. However, the described user actions must be adhered to for best agreement between treatment plan evaluation and the clinical outcome of the delivere
- 2012-09-26FDA-FoodChamberlain Farms Inc.Class IWhole Cantaloupe. Both unlabeled and labeled "MIDWEST BEST" PRODUCE INC. HOMEGROWN CANTALOUPE #4319 PRODUCT OF THE USA
Chamberlain Farm Produce, Inc., of Owensville, Indiana, is voluntarily recalling all of its cantaloupes from the 2012 growing season that may remain in the marketplace. This recall is occurring because of concern some that cantaloupes may be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with
- 2012-09-26FDA-FoodGMP Laboratories of America IncClass IIDietary supplement. Product is labeled as :" Rescue Me***911 Damage Control***brantley living herbal formulas***HERBAL SUPPLEMENT 15 INDIVIDUAL PACKETS 4 VEGAN CAPSULES PER PACKET (2-368mg/2-584mg Each)***DISTRIBUTED EXCLUSIVELY BY: Living Herbal Pharmacy, LLC PO Box 56-2410, Miami, FL 33256-2410***".
The firm recalled because the product lot contained mispackaged product wherein some capsules were missing from the finished packaged product.
- 2012-09-26CPSCAnji Jiayi Garden Supplies Company, Xiaofeng Town, ChinaBig Lots Recalls Garden Swings Due to Fall Hazard
The wooden swing's seat can break while in use, posing a fall hazard to the consumer.
- 2012-09-19FDA-FoodAtlas Operations, Inc.Class IIMeal Replacement product is labeled in part: "***The Perfect Shake***All of the Best***None of the Rest***foru***Dietary supplement***Net wt. 20 oz (1 lb 4 oz) (564 g)***A well balanced blend of old-world plant nutrition.***What's in The Perfect Shake supplement? All of the best, and none of the rest, in amounts that are the right balance for you.***More than just the best ingredients, The perfect Shake supplement is made from the optimal ratio of the right ingredients, scientifically designed
Atlas Operations, Inc is recalling Meal Replacement foru Dietary Supplement, Lot R2-981-12, Exp. Date: 7/14 for possible microbial contamination.
- 2012-09-19FDA-FoodMissa Bay, LLCClass IWawa baby carrots Net Wt 3 oz (85g) Distributed by: Wawa, Inc. Wawa, PA 19063 wawa.com On or before August 16; UPC 2619102517
The products are contaminated with Listeria monocytogenes.
- 2012-09-19FDA-FoodGarden-Fresh Foods, Inc.Class IGarden-Fresh Kidney Bean Salad , 5 lbs., 0 11596 52016
Recalled salads, slaw, salsa, bean and dips contained onions that were recalled by Gills Onions due to potential Listeria monocytogenes contamination.
- 2012-09-19FDA-FoodRon Stockman Whole FoodsClass IThe Thousand Island Chicken Salad Roll is sold at the chef's case, self serve counter, or packaged. Packaged product is labeled as listed below: "***WHOLE FOODS MARKET***1000 ISLAND CHICKEN SALAD ROLL 2 FOR 5***BREAD ( UNBLEACHED UNBROMATED WHEAT OR WHOLE WHEAT FLOUR, WATER, FLORIDA CRYSTALS SUGAR, PALM OIL, EGGS, NON FAT DRY MILK, ASCORBIC ACID, SALT, YEAST, CULTURED WHEAT FLOUR, SOY LECITHIN & NATURAL ENZYMES), CHICKEN ( CHICKEN, WATER, RICE STARCH, SALT), OR TURKEY, CAGE-FREE EGGS (EGGS
Whole Foods Market in Florida recalled certain fresh food items sold in the prepared foods department and one item in the seafood department as they could of been made using raw yellow onions processed by Gill Onions, LLC. Gill Onions, LLC initiated a recall on their product due to possible Listeria monocytogenes contamination.
- 2012-09-19FDA-FoodRon Stockman Whole FoodsClass IRussian Coleslaw is sold at the chef's case, self serve counter, or packaged. Packaged product is labeled as listed below: "***WHOLE FOODS MARKET***RUSSIAN COLESLAW***CABBAGE, CARROTS, THOUSAND DRESSING ( CANOLA MAYONNAISE ( CANOLA OIL, EGGS, FILTERED WATER, HONEY, VINEGAR, SEA SALT, DRY MUSTARD, LEMON JUICE), SWEET PICKLE RELISH ( CUCUMBERS, CRYSTALLIZED CANE JUICE, WATER, DISTILLED VINEGAR, SALT, DEHYDRATED PEPPERS, CALCIUM CHLORIDE, XANTHAN GUM, NATURAL SPICE FLAVORS, GUM ARABIC), SWEET
Whole Foods Market in Florida recalled certain fresh food items sold in the prepared foods department and one item in the seafood department as they could of been made using raw yellow onions processed by Gill Onions, LLC. Gill Onions, LLC initiated a recall on their product due to possible Listeria monocytogenes contamination.
- 2012-09-19FDA-FoodRon Stockman Whole FoodsClass IThe product listed below is prepared at Whole Foods Market and distributed in their retail chef's case or on the self-service bar. It was not sold labeled. BABY SHRIMP SALAD
Whole Foods Market in Florida recalled certain fresh food items sold in the prepared foods department and one item in the seafood department as they could of been made using raw yellow onions processed by Gill Onions, LLC. Gill Onions, LLC initiated a recall on their product due to possible Listeria monocytogenes contamination.
- 2012-09-18CPSCH&M Hennes & Mauritz, New York, N.Y.H&M Recalls Children's Water Bottle Due to Choking Hazard, Sold Exclusively at H&M Stores
The water bottle's spout can break off, posing a choking hazard to children.
- 2012-09-12FDA-DeviceNewport Medical Instruments IncClass INewport HT70 and HT70 Plus Ventilators, Model Number: HT70 and HT70 Plus. Product Usage: The HT70 ventilator system is intended to provide continuous or intermittent positive pressure mechanical ventilatory support for the care of individuals who require mechanical ventilation through invasive or non-invasive interfaces. Specifically, the HT70 family of ventilators is applicable for infant, pediatric and adult patients greater than or equal to 5 kg (11 lbs.). The HT70 is a restricted medica
May emit a continuous high priority alarm and the ventilator may stop ventilating, due to a component failure on the control board.
- 2012-09-12FDA-FoodDrucker Labs LPClass IIintraKID Lot 658 with a Best By date of 12/12, 33 oz and 2 oz bottles
After extensive testing and investigation, Drucker Labs has determined that an incorrect form of Vitamin B3, Nicotinic Acid, was used in the manufacturing of intraKID Lot 658. This nutrient may cause a temporary symptom in a small number of consumers. This symptom, commonly known as Niacin Flush, may include itching, redness, or warmth of the skin. This typically subsides within 15 20 minut
- 2012-09-06CPSCBlind Xpress of Livonia, Mich.Death of Child Prompts Recall of Window Blinds by Blind Xpress
The vertical blinds have an adjustment cord that forms a loop that is not attached to the wall or floor. In some instances, this loop has a weighted device at the bottom. The horizontal blinds do not have inner cord stop devices to prevent the accessible inner cords from being pulled out. A child can become entangled in a cord loop and strangle.
- 2012-09-05FDA-DeviceBaxter Healthcare Corp.Class IIIMini-Infuser Model 300XL Multispeed Infusion Pump, an Rx battery operated syringe infusion pump with an active time scale and rate selector switch; product codes 2M8171 and 2M8171R. Product Usage: These product codes includes refurbished units. Intended for the controlled rate delivery of small volume parental fluids as prescribed by a physician. Usage: The Mini-Infuser System is designed for controlled intermittent administration of intravenous medication.
Should a battery with the minimum contact diameter (.51 inches) be placed on the battery spring (.53 inches), an electrical circuit will not be completed and the Mini-Infuser will not operate. The reason being that the Mini-Infuser Battery Spring has a flat contact that measures .53 inches ¿.01 inches on the inner diameter of the spring coil. The IEC 60086-2 and ANSI 08 standards specify a minimum
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