Baby and kids' product recalls
6672 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.
- 2016-09-21FDA-FoodSunOpta Food and Grain, Inc.Class IEXPANDED 5/18/2016 DAKOTA STYLE Salted Caramel sunflower kernel 2000 lbs. Poly Lined - Poly Woven Tote, Product of USA, Manufactured by SunOpta, Crookston, MN
SunOpta is recalling sunflower kernel products that have the potential to be contaminated with Listeria monocytogenes. EXPANDED 5/18/2016 SunOpta expanded their recall of roasted sunflower kernel products to include the production dates of February 20 - April 26, 2016 due to potential Listeria monocytogenes contamination. 2nd EXPANSION 5/31/2016 SunOpta expanded their recall to include product produced at their Crookston, MN facility, still within expiry, to include the production dates of May 31, 2015 thru January 31, 2016
- 2016-09-21FDA-FoodSunOpta Food and Grain, Inc.Class IDAKOTA STYLE SAVORY BACON sunflower kernel 2000 lbs. Poly Lined - Poly Woven Tote, Product of USA, Manufactured by SunOpta, Crookston, MN
SunOpta is recalling sunflower kernel products that have the potential to be contaminated with Listeria monocytogenes. EXPANDED 5/18/2016 SunOpta expanded their recall of roasted sunflower kernel products to include the production dates of February 20 - April 26, 2016 due to potential Listeria monocytogenes contamination. 2nd EXPANSION 5/31/2016 SunOpta expanded their recall to include product produced at their Crookston, MN facility, still within expiry, to include the production dates of May 31, 2015 thru January 31, 2016
- 2016-09-21FDA-FoodSunOpta Food and Grain, Inc.Class I1. Roasted Not Salted Sunflower Kernel, 5 lbs (2.25 kgs) box, Manufactured by SunOpta, Crookston, MN; 2. Roasted Not Salted Sunflower Kernels, 25 lbs (11.34 kgs) poly lined paper bag, Manufactured by SunOpta, Crookston, MN; 3. Roasted Not Salted SL-80 Sunflower Kernels, 45 lbs vacuum packed bag in box, Manufactured by SunOpta, Crookston, MN; 4. Roasted Not Salted Sunflower Kernel, 50 lbs. bag, Product of USA, Manufactured by SunOpta, Crookston, MN; EXPANDED 5/18/2016 Roasted
SunOpta is recalling sunflower kernel products that have the potential to be contaminated with Listeria monocytogenes. EXPANDED 5/18/2016 SunOpta expanded their recall of roasted sunflower kernel products to include the production dates of February 20 - April 26, 2016 due to potential Listeria monocytogenes contamination. 2nd EXPANSION 5/31/2016 SunOpta expanded their recall to include product produced at their Crookston, MN facility, still within expiry, to include the production dates of May 31, 2015 thru January 31, 2016.
- 2016-09-21FDA-FoodSunOpta Food and Grain, Inc.Class I1. Roasted & Salted Sunflower Kernel, 0.7 oz plastic bag, Distributed by Newport Ingredients, Los Angeles, CA 90036; 2. Planters Sunflower Kernels, Net Wt 3 oz. (85g) plastic bag; 3. Dakota's Best! Biggy'z Roasted & Salted Kernels, Net Wt 16 oz (454g) plastic bag; 4. Roasted & Salted Sunflower Kernels, 5 lbs (2.25 kgs) box, Manufactured by SunOpta, Crookston, MN; 5. Roasted & Salted Sunflower Kernels, 25 lbs (11.34 kgs) poly lined paper bag, Manufactured by SunOpta, Crookston, MN; 6.
SunOpta is recalling sunflower kernel products that have the potential to be contaminated with Listeria monocytogenes. EXPANDED 5/18/2016 SunOpta expanded their recall of roasted sunflower kernel products to include the production dates of February 20 - April 26, 2016 due to potential Listeria monocytogenes contamination. 2nd EXPANSION 5/31/2016 SunOpta expanded their recall to include product produced at their Crookston, MN facility, still within expiry, to include the production dates of May 31, 2015 thru January 31, 2016
- 2016-09-21FDA-FoodUltimate Nutrition, Inc.Class IULTIMATE NUTRITION AMINO GOLD CAPSULES SUPER WHEY FORMULA Dietary Supplement, 1000 mg, 250 tablets; UPC: 0 99071 00140 5
Product contains undeclared milk.
- 2016-09-21FDA-FoodUltimate Nutrition, Inc.Class IULTIMATE NUTRITION AMINO GOLD TABLETS SUPER WHEY FORMULA Dietary Supplement 1000 mg 250 capsules; UPC: 099071 00120 7
Product contains undeclared milk.
- 2016-09-21FDA-FoodUltimate Nutrition, Inc.Class IULTIMATE NUTRITION AMINO GOLD TABLETS SUPER WHEY FORMULA Dietary Supplement 1500 mg 325 tablets
Product contains undeclared milk.
- 2016-09-21CPSCLenny Lamb, of PolandInfant Carriers Recalled Due to Fall Hazard; Manufactured By Lenny Lamb
The internal stitching on the infant carrier is missing, posing a fall hazard to children.
- 2016-09-16USDAClass IDo not eat Bungie's Meats pork sausage
Unfit for Human Consumption
- 2016-09-08CPSCToys 'R' Us Inc., of Wayne, N.J.Toys 'R' Us Recalls Pacifier Clips Due to Choking Hazard; Sold Exclusively at Babies 'R' Us and Toys 'R' Us
The pacifier clip's spring mechanism can break and release small parts, posing a choking hazard.
- 2016-09-07NHTSA-EquipmentEvenflo Company, Inc.Evenflo Company, Inc. — Child Can Access/Loosen Harness Adjustment Button
If the child is able to loosen the harness, they may not be properly secured in the event of a crash, increasing their risk of injury.
- 2016-08-31FDA-DeviceVision RT LtdClass IIAlignRT¿ Plus [private label-OSMS] K123371: The AlignRT Plus system is indicated for use to position and monitor patients relative to the prescribed treatment isocentre, and to withhold the beam automatically during radiation delivery.
Vision RT Ltd received three (3) reports from different sites that discovered the following issue, unintended changes were made to planned couch parameters, specifically the couch rotation parameter, during patient set-up for the Optical Surface Monitoring System [OSMS]. 1. CRM 3194, No Serious Injury, No MDR, Aware date: Dec 11, 2015 2. CRM 3321, No Patient Involved, No MDR, Aware date: Jan 19, 2016 3. CRM 4570, No Serious Injury, No MDR, Aware date: March 15, 2016 No patient harm was reported in any of these cases.
- 2016-08-30CPSCJW Crawford, Inc., of Monroe, N.Y.Dazzling Toys Recalls Chicken Toys Due to Choking Hazard (Recall Alert)
The toys contain small eggs and the chicken can break into small plastic pieces, both posing a choking hazard to children.
- 2016-08-25CPSCPhillips International Inc., of Hallandale, Fla.Mars Retail Group Recalls M&M'S-Branded Jewelry Due to Violation of Lead Standard
The jewelry can contain high levels of lead. Lead is toxic if ingested by young children and can cause adverse health issues.
- 2016-08-24FDA-DeviceAvid Medical, Inc.Class IIPEDIATRIC KIDNEY BIOPSY TRAY
Avid Medical Inc. states a latex-containing Telfa" Non-adherent Dressing 4"x3" (10.2cm x 7.6 em) was included in a limited number of convenience kits (custom procedure trays) that were not labeled as containing latex.
- 2016-08-24FDA-DeviceBard Peripheral Vascular IncClass IIBard TruGuide Disposable Coaxial Biopsy Needle Mixed Product Part Number C1816B The TruGuide Disposable Coaxial Biopsy Needles are intended for use as a guiding needle in obtaining core biopsy samples from soft tissue such as liver, kidney, spleen, lymph nodes and various soft tissue lesions.
May contain two trocar tip stylets with coaxials or two blunt tip stylets instead of one of each.
- 2016-08-24CPSCDorel Juvenile, of Columbus, Ind.Dorel Juvenile Recalls Safety 1st Strollers Due to Fall Hazard
The stroller tray folding mechanism can partially disengage on one side when used with an infant car seat attached to the stroller, posing a fall hazard.
- 2016-08-23CPSCALEX Toys, New JerseyAlex Toys Recalls Infant Building Play Sets Due to Choking Hazard
Small parts of the plastic toy building sets can detach, posing a choking hazard to young children.
- 2016-08-23CPSCMcDonald's Corp., of Oakbrook, Ill.McDonald’s Recalls “Step-iT” Activity Wristbands Due to Risk of Skin Irritation or Burns
The recalled wristbands can cause skin irritation or burns to children.
- 2016-08-17FDA-DrugTeva North AmericaClass IIAlbuterol Sulfate Syrup, 2 mg/ 5 mL, 473 mL bottle, Rx only, Manufactured in Canada by Contract Pharmaceuticals Limited, Canada, Manufactured For: Teva Pharmaceuticals USA, Sellersville, PA --- NDC 0093-0661-16
Presence of Foreign Substance; presence of black particles describes generically as cellulose-based bundles of brown fibrous material.
- 2016-08-17CPSCXenith LLC, of Detroit, Mich.Xenith Recalls Football Helmets Due to Head Injury Hazard
The shells of the football helmets can crack, posing a risk of head injuries to football players.
- 2016-08-16CPSCSauder Woodworking Co., of Archbold, OhioSauder Woodworking Recalls Chest of Drawers Due to Serious Tip-Over Hazard; Sold Exclusively at Walmart.com (Recall Alert)
The recalled chests are unstable unless they are properly anchored to the wall, posing a serious tip-over and entrapment hazard that could result in death or serious injuries to children. Due to a manufacturing problem, these chests do not comply with the voluntary safety standard (ASTM F2057-14).
- 2016-08-10FDA-DeviceB-K Medical A/SClass IIBK Medical ApS Ultrasound System Scanner bk2300 - Model #: bk3500 with software releases 1.2.0, 1.2.1 and 1.2.2. The system is intended for diagnostic ultrasound imaging or fluid flow analysis of the human body, data processing and guidance of puncture and biopsy. The system performs simple geometric measurements and calculations in the following areas: Emergency Medicine, Anesthesia, MSK, Vascular, Cardiology, OB/GYN
In the system (bk3500) software generic volume measurement (HxWxLxl) function the user may be unaware of the calculation factor (1) and assume the generic volume calculation factor is similar to that of the other (prostate, adenoma, testis, kidney, and bladder) volume calculation factors provided in the software.
- 2016-08-10FDA-DrugTeva North AmericaClass IIIChildren's Qnasl 40 mcg (beclomethasone dipropionate) Nasal Aerosol, 40 mcg per spray, 60 Metered Sprays per canister, 4.9g Net Contents, Rx only; Professional Sample; Manufactured for Teva Respiratory, LLC, Horsham, PA 19044; By: 3M Drug Delivery Systems, Northridge, CA 91324; NDC 59310-206-08.
Failed Content Uniformity Specifications: out of specification test result for spray content uniformity.
- 2016-08-04CPSCCinmar LLC, of West Chester, OhioCinmar Recalls World Magnetic Travel Maps Due To Risk of Magnet Ingestion by Children; Sold Exclusively at Frontgate (Recall Alert)
When two or more magnets are swallowed, they can link together inside the intestines and clamp onto body tissues, causing intestinal obstructions, perforations, sepsis and death. Internal injury from magnets can pose serious lifelong health effects.
- 2016-08-03FDA-DeviceDraeger Medical, Inc.Class IIBabytherm 8004/8010, Infant Warmer, Class II device, 510 K K971198, Catalog # FR00105 (Babytherm 8010), 2M30404 (Babytherm 8004), non sterile, software controlled. Product Usage: Babytherm 8004/8010 is an open care infant warmer system for warming premature babies, neonates and infants with a body weight of up to 8 kg (17.6 lbs). The device is intended for use in delivery rooms, operating rooms, maternity and obstetric units, neonatal and pediatric wards, neonatal and pediatric intensive car
Risk associated with operating the device in skin temperature mode with temperature sensors attached but no patient connected.
- 2016-08-03FDA-DeviceAlere San Diego, Inc.Class IIISignify Mono (Whole Blood, Serum, Plasma), Catalog No. 01P52-25 a simple test that utilizes an extract of bovine erythrocytes to qualitatively and selectively detect IM heterophile antibodies in whole blood, serum or plasma in just minutes.
The Positive Control information referencing human plasma as the antibody material described in the product labeling and packaging is incorrect.
- 2016-08-03FDA-DeviceAlere San Diego, Inc.Class IIIStanbio Rely Mono Rapid Test, Catalog No. 6200-010L and 6200-020L a simple test that utilizes an extract of bovine erythrocytes to qualitatively and selectively detect IM heterophile antibodies in whole blood, serum or plasma in just minutes.
The Positive Control information referencing human plasma as the antibody material described in the product labeling and packaging is incorrect.
- 2016-08-03FDA-DeviceAlere San Diego, Inc.Class IIIProadvantage Mono Rapid Test Cassette, Catalog No. P080016 a simple test that utilizes an extract of bovine erythrocytes to qualitatively and selectively detect IM heterophile antibodies in whole blood, serum or plasma in just minutes.
The Positive Control information referencing human plasma as the antibody material described in the product labeling and packaging is incorrect.
- 2016-08-03FDA-DeviceAlere San Diego, Inc.Class IIIHenry Schein One Step + Mono Rapid Test Device, Catalog No. 9004070 a simple test that utilizes an extract of bovine erythrocytes to qualitatively and selectively detect IM heterophile antibodies in whole blood, serum or plasma in just minutes.
The Positive Control information referencing human plasma as the antibody material described in the product labeling and packaging is incorrect.
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