Baby and kids' product recalls
6674 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.
- 2012-11-16CPSCKidCo Inc., of Libertyville, Ill.Suffocation, Entrapment Risks Prompt Recall of PeaPod Travel Tents by KidCo
Infants and young children can roll off the edge of the inflatable air mattress, become entrapped between the mattress and the fabric sides of the tent, and suffocate.
- 2012-11-14FDA-DevicePhilips Medical Systems (Cleveland), Inc.Class IIPinnacle3 VCC P/N 4598 001 41341 REV A, Philips Medical Systems (Cleveland), Inc., Fitchburg, WI. Pinnacle3 Radiation Therapy Planning System is a computer software package intended to provide support for radiation therapy treatment planning for the treatment of benign or malignant disease processes. Pinnacle3 Radiation Therapy Planning System assists the clinician in formulating a treatment plan that maximizes the dose to the treatment volume while minimizing the dose to the surrounding norm
Philips Medical Systems Cleveland), Inc. is recalling Pinnacle3 Virtual Client Connection software version 3.1 due to an improper release and subsequent distribution.
- 2012-11-14FDA-FoodNatural Selection Foods LLC dba Earthbound FarmClass IEarthbound Farms Organic Baby Spinach Grab & Go Salad; with sesame, soy vinaigrette and peanuts. USDA Organic 3.5 oz. Clamshell package. UPC 0 32601 08875 0 Natural Selection Foods San Juan Bautista, CA.
Peanuts packaged with EarthBound Baby Spinach Grab & Go Salad were provided by Sunland through a third party and are under recall due to potential Salmonella contamination.
- 2012-11-08CPSCLaJobi, Inc., of Cranbury, N.J.LaJobi Recalls Glider Rockers Due to Fall Hazard
The base of the glider rocker can crack or break, posing a fall hazard.
- 2012-11-07FDA-DeviceVentlab CorporationClass IAirFlow, Infant Resuscitator, AF3000 Series, Single use, Manufactured by: Ventlab Corporation, 155 Boyce Drive, Mockville, NC 27028 The Disposable Resuscitators with optional built-in pressure monitor is intended to provide respiratory support in the presence of reversible apnea, commonly associated with cardiopulmonary arrest.
Possible volume leakage through the inlet valve during compressions of the resuscitator bag.
- 2012-11-07FDA-DeviceVentlab CorporationClass IVentlab Rescue Med Infant Resuscitator, Manufactured by: Ventlab Corporation, 155 Boyce Drive, Mockville, NC 27028. The Disposable Resuscitators with optional built-in pressure monitor is intended to provide respiratory support in the presence of reversible apnea, commonly associated with cardiopulmonary arrest.
Possible volume leakage through the inlet valve during compressions of the resuscitator bag.
- 2012-11-07FDA-DeviceVentlab CorporationClass IVentlab Premium Small Child Resuscitator, Manufactured by: Ventlab Corporation, 155 Boyce Drive, Mockville, NC 27028.
Possible volume leakage through the inlet valve during compressions of the resuscitator bag.
- 2012-11-07FDA-DeviceVentlab CorporationClass ISafe Spot Infant Resuscitator, Pro-1900 Series, Single Patient Use, The Disposable Resuscitators with optional built-in pressure monitor is intended to provide respiratory support in the presence of reversible apnea, commonly associated with cardiopulmonary arrest.
Possible volume leakage through the inlet valve during compressions of the resuscitator bag.
- 2012-11-07FDA-DeviceVentlab CorporationClass IBreath Tech, Safe Spot Infant Resuscitator, BT2000 Series, Single use, Manufactured by: Ventlab Corporation, 155 Boyce Drive, Mockville, NC 27028. The Disposable Resuscitators with optional built-in pressure monitor is intended to provide respiratory support in the presence of reversible apnea, commonly associated with cardiopulmonary arrest.
Possible volume leakage through the inlet valve during compressions of the resuscitator bag.
- 2012-11-07FDA-DeviceVentlab CorporationClass IV*Care Resuscitator Infant Resuscitator, VN 3000 Series, Single use, Manufactured by: Ventlab Corporation, 155 Boyce Drive, Mockville, NC 27028. The Disposable Resuscitators with optional built-in pressure monitor is intended to provide respiratory support in the presence of reversible apnea, commonly associated with cardiopulmonary arrest.
Possible volume leakage through the inlet valve during compressions of the resuscitator bag.
- 2012-11-07FDA-DeviceVentlab CorporationClass ISafe Spot Infant Resuscitator, SS3200 Series, Single Patient Use, Manufactured by: Ventlab Corporation, 155 Boyce Drive, Mockville, NC 27028. The Disposable Resuscitators with optional built-in pressure monitor is intended to provide respiratory support in the presence of reversible apnea, commonly associated with cardiopulmonary arrest.
Possible volume leakage through the inlet valve during compressions of the resuscitator bag.
- 2012-11-07FDA-DeviceElekta, Inc.Class IIMOSAIQ MOSAIQ is an image-enabled electronic medical record system (EMR) used for oncology workflow management. It lets users supply electronic patient charts and assemble care plans, order diagnostic tests, and prescribe medications. It also lets users import, view, annotate, manipulate, enhance, manage, and archive images.
A patient was seriously mistreated after a user made and saved an inadvertent change to the definition of a treatment filed in MOSAIQ.
- 2012-11-07FDA-DrugDermaCare, Inc.Class IIUP & UP brand, kid's foaming hand sanitizer, alcohol free, 99.9% effective against germs, Sweet s'melon, 6.7FL oz (200mL), Distributed by Target Corp., Minneapollis, MN 55403
Microbial Contamination of Non-Sterile Products: Laboratory findings of high total plate count above specification.
- 2012-11-07FDA-DrugDermaCare, Inc.Class IIUP & UP brand, kid's foaming hand sanitizer, alcohol free, 99.9% effective against germs, Apple-cleani, 6.7FL oz (200mL), Distributed by Target Corp., Minneapollis, MN 55403
Microbial Contamination of Non-Sterile Products: Laboratory findings of high total plate count above specification.
- 2012-11-02NHTSA-EquipmentBritax Child Safety, Inc.Britax Child Safety, Inc. — Possible Choking Hazard
If the child bites off a piece of the softer pad, it could be a choking hazard, resulting in injury or death.
- 2012-10-31FDA-FoodSunland, IncorporatedClass IPeanut Power Butter, Original Formula Net Wt. 16 oz, UPC 5855200003, Manufactured for PB, Inc,. PO BOX 661346, Birmingham, AL 35216. Labeling is black, yellow and white with white, black, yellow and red print writing. Also, Net Wt. 4 lb, UPC 5855200007, Distributed by SNACLite LLC, PO Box 830770, Birmingham, AL 35283.
Sunland, Inc. is conducting a voluntary limited recall of its Almond, Peanut, and Cashew Butter products and Tahini and Roasted Blanched Peanut Products, manufactured between May 1, 2010 and September 24, 2012, because these products may be contaminated with Salmonella.
- 2012-10-24FDA-DeviceTerumo Cardiovascular Systems CorporationClass IITerumo Backplate Replacement CXFVR 1500 Holder The Flexible venous Reservoir is mounted on the Backplate/Holder and secures the flexible reservoir by strategically placed mounting arms. Additionally, there are three port supports the user incorporates to position the lines that enter and exit the venous bag. The Backplate/Holder is designed to allow the user to move the port support location to accommodate different tubing circuit designs to permit mounting flexibility.
Backplate reservoir holders were manufactured with an incorrect configuration of connector supports. The devices were manufactured and configured with two 3/8 inch and one ¿ inch connector supports instead of one 3/8 inch and two ¿ inch connector supports (See location of supports as # 7 and # 8 on backplate attachment). The backplates were manufactured as described in manufacturing instructions a
- 2012-10-24FDA-FoodBottling LLC dba Pepsi Beverages CompanyClass IIDiet Crush Orange Soda, 12 oz cans
Dr Pepper/Seven Up, Inc. has initiated a recall of mislabeled Diet Crush Orange Soda produced under license issued by one of their licensed bottlers, Pepsi Beverages Company in Phoenix, Arizona. The bottler used new graphics on cans of product made with the previous formulation which is in the process of being discontinued.
- 2012-10-24FDA-FoodWhole Foods MarketClass IFrescolina and Mitica brand Ricotta Salata cheeses were cut into wedges, packaged in clear plastic wrap and sold with a Whole Foods Market scale label using PLU 293427 and PLU 294413, respectively. All "sell by" dates through Oct. 2 are affected.
Whole Foods Market announces that it is recalling ricotta salata sold in 21 states and Washington, D.C. that came from its supplier Forever Cheese Inc. of Long Island City, NY. Forever Cheese recalled this cheese product because it may be contaminated with Listeria monocytogenes. Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail
- 2012-10-24FDA-DrugSandoz IncorporatedClass IIIChildren's Cetirizine HCl Chewable Tablets 5 mg, 30 count blister pack, Manufactured in India by Sandoz Private Ltd., for Sandoz Inc., Princeton, NJ NDC 0781-5283-64 --- ALSO sold under Major brand All Day Allergy Children's Cetirizine HCl 5 mg, 5 count blister pack, Major Pharmaceuticals, Livonia, MI NDC 0904-5878-33
Impurity/Degradation; exceeded impurity specification at the 8 and 15 month time points (betacyclodextrin ester 1&2)
- 2012-10-24CPSCRivers Edge Tree Stands Inc., of Cumberland, Wis.Rivers Edge Recalls Hunters Tree Stands due to Fall Hazard
The snap-hook assemblies can fail, causing the tree stand and the user to fall to the ground.
- 2012-10-23CPSCDorel Juvenile Group, of Columbus, Ind.Dorel Juvenile Group Recalls Eddie Bauer Rocking Wood Bassinets Due to Infant Suffocation Hazard
The bottom locking mechanism can fail to lock properly if a spring is not installed, allowing the bassinet to tip to one side and cause infants to roll to the side of the bassinet. This poses a suffocation hazard to infants.
- 2012-10-23CPSCUnique Baby Products USA LLC, d/b/a ValcoBaby, of Brooklyn, N.Y.ValcoBaby Booster Seats Recalled Due to Fall Hazard
The spring button mechanism securing the booster toddler seat to the baby stroller can disengage, allowing for the carried toddler to fall.
- 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.
Get notified about new baby recalls
Free weekly digest. We email when a new federal recall in this category — or anything else affecting your household — is published.
Get the Sunday Brief