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.
- 2021-05-26FDA-DeviceBard Access Systems Inc.Class IIREF 7617407, Groshong NXT ClearVue Catheter, Full Kit, 4F, Single-Lumen, 60 cm, UDI: (01)10801741035248 - Product Usage: is designed for use when central venous catheterization is prescribed.
Catheters contain two issues: 1. the inner diameter of the distal connector may be reduced resulting in inability to pass the catheter through the connector and 2. the catch slot on the distal connecter may be deformed resulting in the inability to properly lock
- 2021-05-26FDA-DeviceBard Access Systems Inc.Class IIREF 7617405, Groshong NXT ClearVue Catheter Basic Kit, 4F, Single-Lumen, 60 cm, UDI: (01)10801741086998 - Product Usage: is designed for use when central venous catheterization is prescribed.
Catheters contain two issues: 1. the inner diameter of the distal connector may be reduced resulting in inability to pass the catheter through the connector and 2. the catch slot on the distal connecter may be deformed resulting in the inability to properly lock
- 2021-05-26FDA-DeviceBard Access Systems Inc.Class IIREF CK000516, Groshong NXT ClearVue Catheter with Sherlock 3CG Tip Positioning System (TPS) Stylet, Full Kit, 4F, Single-Lumen, TPS, CE 2797, UDI: (01)10801741107891 - Product Usage: is designed for use when central venous catheterization is prescribed.
Catheters contain two issues: 1. the inner diameter of the distal connector may be reduced resulting in inability to pass the catheter through the connector and 2. the catch slot on the distal connecter may be deformed resulting in the inability to properly lock
- 2021-05-26FDA-DeviceBard Access Systems Inc.Class IIREF CK000379, Groshong NXT ClearVue Catheter with Sherlock Tip Location System (TLS) Stylet, Full Kit, 4F, Single-Lumen, TLS, CE 2797, UDI: (01)10801741102704 - Product Usage: is designed for use when central venous catheterization is prescribed.
Catheters contain two issues: 1. the inner diameter of the distal connector may be reduced resulting in inability to pass the catheter through the connector and 2. the catch slot on the distal connecter may be deformed resulting in the inability to properly lock
- 2021-05-26FDA-DeviceBard Access Systems Inc.Class IIREF 91660417, Groshong NXT ClearVue Catheter with Sherlock 3CG Tip Positioning System (TPS) Stylet Tip, Basic Kit, 4F, Single-Lumen, TPS, CE 2797, UDI: (01)10801741107822 - Product Usage: is designed for use when central venous catheterization is prescribed.
Catheters contain two issues: 1. the inner diameter of the distal connector may be reduced resulting in inability to pass the catheter through the connector and 2. the catch slot on the distal connecter may be deformed resulting in the inability to properly lock
- 2021-05-26FDA-DeviceBard Access Systems Inc.Class IIREF 69655405, Groshong NXT ClearVue Catheter with Sherlock Tip Location System (TLS) Stylet, Basic Kit, 4F, Single-Lumen, TLS, UDI: (01)10801741147521 - Product Usage: is designed for use when central venous catheterization is prescribed.
Catheters contain two issues: 1. the inner diameter of the distal connector may be reduced resulting in inability to pass the catheter through the connector and 2. the catch slot on the distal connecter may be deformed resulting in the inability to properly lock
- 2021-05-26FDA-DeviceBard Access Systems Inc.Class IIREF 9655405, Groshong NXT ClearVue Catheter with Sherlock Tip Location System (TLS) Stylet, Basic Kit, 4F, Single-Lumen, TLS, UDI: (01)10801741036023 - Product Usage: is designed for use when central venous catheterization is prescribed.
Catheters contain two issues: 1. the inner diameter of the distal connector may be reduced resulting in inability to pass the catheter through the connector and 2. the catch slot on the distal connecter may be deformed resulting in the inability to properly lock
- 2021-05-26FDA-DeviceBard Access Systems Inc.Class IIREF 9617408D, Groshong NXT ClearVue Catheter with Sherlock Tip Location System (TLS) Stylet, Maximal Barrier Kit, 4F, Single-Lumen, TLS, UDI: (01)10801741036016 - Product Usage: is designed for use when central venous catheterization is prescribed.
Catheters contain two issues: 1. the inner diameter of the distal connector may be reduced resulting in inability to pass the catheter through the connector and 2. the catch slot on the distal connecter may be deformed resulting in the inability to properly lock
- 2021-05-26FDA-DeviceBard Access Systems Inc.Class IIREF 9617408, Groshong NXT ClearVue Catheter with Sherlock Tip Location System (TLS) Stylet, Full Kit, 4F, Single-Lumen, TLS, UDI: (01)10801741036009 - Product Usage: is designed for use when central venous catheterization is prescribed.
Catheters contain two issues: 1. the inner diameter of the distal connector may be reduced resulting in inability to pass the catheter through the connector and 2. the catch slot on the distal connecter may be deformed resulting in the inability to properly lock
- 2021-05-26FDA-DeviceBard Access Systems Inc.Class IIREF 9617407, Groshong NXT ClearVue Catheter with Sherlock Tip Location System (TLS) Stylet, Full Kit, 4F, Single-Lumen, TLS, UDI: (01)10801741035996 - Product Usage: is designed for use when central venous catheterization is prescribed.
Catheters contain two issues: 1. the inner diameter of the distal connector may be reduced resulting in inability to pass the catheter through the connector and 2. the catch slot on the distal connecter may be deformed resulting in the inability to properly lock
- 2021-05-26FDA-DeviceBard Access Systems Inc.Class IIREF 9617405, Groshong NXT ClearVue Catheter with Sherlock Tip Location System (TLS) Stylet, Basic Kit, 4F, Single-Lumen, TLS, UDI: (01)10801741035989 - Product Usage: is designed for use when central venous catheterization is prescribed.
Catheters contain two issues: 1. the inner diameter of the distal connector may be reduced resulting in inability to pass the catheter through the connector and 2. the catch slot on the distal connecter may be deformed resulting in the inability to properly lock
- 2021-05-26FDA-DeviceBard Access Systems Inc.Class IIREF 7812400, Replacement Connector For 4F Groshong NXT clearVue PICC with Extension Leg, Rx Only, Sterile EO, CE 2797, UDI: (01)10801741075268 - Product Usage: is designed for use when central venous catheterization is prescribed.
Catheters contain two issues: 1. the inner diameter of the distal connector may be reduced resulting in inability to pass the catheter through the connector and 2. the catch slot on the distal connecter may be deformed resulting in the inability to properly lock
- 2021-05-26FDA-DeviceBard Access Systems Inc.Class IIREF 7655405J, Groshong NXT ClearVue Catheter, Basic Kit, 4F, Single-Lumen, 60 cm, UDI: (01)10801741200615 - Product Usage: is designed for use when central venous catheterization is prescribed.
Catheters contain two issues: 1. the inner diameter of the distal connector may be reduced resulting in inability to pass the catheter through the connector and 2. the catch slot on the distal connecter may be deformed resulting in the inability to properly lock
- 2021-05-26FDA-DeviceBard Access Systems Inc.Class IIREF 7655405, Groshong NXT ClearVue Catheter, Basic Kit, 4F, Single-Lumen, 60 cm, UDI: (01)10801741035279 - Product Usage: is designed for use when central venous catheterization is prescribed.
Catheters contain two issues: 1. the inner diameter of the distal connector may be reduced resulting in inability to pass the catheter through the connector and 2. the catch slot on the distal connecter may be deformed resulting in the inability to properly lock
- 2021-05-26FDA-DeviceBard Access Systems Inc.Class IIREF 7617408D, Groshong NXT ClearVue Catheter, Maximal Barrier Kit, 4F, Single-Lumen, 60 cm, UDI: (01)10801741035262 - Product Usage: is designed for use when central venous catheterization is prescribed.
Catheters contain two issues: 1. the inner diameter of the distal connector may be reduced resulting in inability to pass the catheter through the connector and 2. the catch slot on the distal connecter may be deformed resulting in the inability to properly lock
- 2021-05-26FDA-DeviceBard Access Systems Inc.Class IIREF 7617408, Groshong NXT ClearVue Catheter, Full Kit, 4F, Single-Lumen, 60 cm, UDI: (01)10801741035255 - Product Usage: is designed for use when central venous catheterization is prescribed.
Catheters contain two issues: 1. the inner diameter of the distal connector may be reduced resulting in inability to pass the catheter through the connector and 2. the catch slot on the distal connecter may be deformed resulting in the inability to properly lock
- 2021-05-26FDA-DeviceBard Access Systems Inc.Class IIREF 7617405J, Groshong NXT ClearVue Catheter, Basic kit, 4F, Single-Lumen, 60 cm, UDI: (01)10801741200592 - Product Usage: is designed for use when central venous catheterization is prescribed.
Catheters contain two issues: 1. the inner diameter of the distal connector may be reduced resulting in inability to pass the catheter through the connector and 2. the catch slot on the distal connecter may be deformed resulting in the inability to properly lock
- 2021-05-26FDA-DeviceBard Access Systems Inc.Class IIREF 7617400, Groshong NXT ClearVue Catheter, intermediate kit, 4F, Single-Lumen, 60 cm, UDI: (01)10801741045094 - Product Usage: is designed for use when central venous catheterization is prescribed.
Catheters contain two issues: 1. the inner diameter of the distal connector may be reduced resulting in inability to pass the catheter through the connector and 2. the catch slot on the distal connecter may be deformed resulting in the inability to properly lock
- 2021-05-26FDA-DrugSigmaPharm Laboratories LLCClass IIIAsenapine Sublingual Tablets, 10 mg, Rx only, 60 Tablets, Sigmapharm Laboratories, LLC, Bensalem, PA, 19020, NDC 42794-017-10
Incorrect Product Formulation; product was manufactured with the incorrect Art Cherry Flavor flavoring agent instead of Art Black Cherry Flavor flavoring agent
- 2021-05-26FDA-DrugSigmaPharm Laboratories LLCClass IIIAsenapine Sublingual Tablets, 5 mg, Rx Only, 60 Tablets, Sigmapharm Laboratories, LLC, Bensalem, PA, 19020 NDC 42794-016-10.
Incorrect Product Formulation; product was manufactured with the incorrect Art Cherry Flavor flavoring agent instead of Art Black Cherry Flavor flavoring agent
- 2021-05-26CPSCJ.C. Penney Purchasing Corporation Inc., of Lewisville, TexasJCPenney Recalls Girls Puffer Jackets Due to Entanglement Hazard
The puffer jackets have a drawstring located inside the lining of the bottom area of the garment. The drawstring can become entangled or caught on playground slides, handrails, school bus doors or other moving objects, posing an entanglement hazard to children.
- 2021-05-26CPSCThe Ergobaby Carrier Inc., of Los Angeles, Calif.Ergobaby Recalls METROUS Strollers Due to Choking Hazard
The button on some buckles that release the harness can break and detach when pressed by the user while the child is in the stroller, making it difficult to release, and posing a choking hazard to young children.
- 2021-05-21USDAClass IMilan Provisions Co. Inc. Recalls Jalapeno Chorizo Sausage Products Formulated With Pork Ingredients Produced Without the Benefit of Inspection
Produced Without Benefit of Inspection
- 2021-05-20CPSCChemical Technologies International Inc., dba Pro Supply Outlet, of Rancho Cordova, Calif.Pro Supply Outlet Recalls Sodium and Potassium Hydroxide Products Due to Failure to Meet Child-Resistant Packaging Requirement and Violation of FHSA Labeling Requirement (Recall Alert)
The products contain sodium hydroxide or potassium hydroxide which must be in child resistant packaging, as required by the Poison Prevention Packaging Act (PPPA). The packaging of the products is not child resistant, posing a risk of chemical burns and irritation to the skin and eyes. In addition, the label on the product violates the Federal Hazardous Substance Act (FHSA) by omitting the word "poison" for poisonous chemicals.
- 2021-05-13CPSCLeisure Time Products LLC, of Pittsburg, Kan.Leisure Time Products Recalls Brutus Swing Sets Due to Injury Hazard (Recall Alert)
The attachment that connects the swing hanger to the top tube can fail, posing an injury hazard.
- 2021-05-13CPSCThe Lye Guy, of Pennellville, N.Y.The Lye Guy Recalls Sodium and Potassium Hydroxide Products Due to Failure to Meet Child Resistant Packaging Requirement and Violation of FHSA Labeling (Recall Alert)
The products contain sodium and potassium hydroxide, which must be in child resistant packaging as required by the Poison Prevention Packaging Act (PPPA). The packaging of the products is not child resistant, posing a risk of chemical burns and irritation to the skin and eyes. In addition, the label on the products violates the Federal Hazardous Substance Act (FHSA) by omitting the word "poison" and other mandatory information on the packaging.
- 2021-05-13CPSCAlliance Chemical, of Taylor, TexasAlliance Chemical Recalls Sodium Hydroxide Products Due to Failure to Meet Child Resistant Packaging Requirement and Violation of FHSA Labeling (Recall Alert)
The products contain sodium hydroxide, which must be in child resistant packaging as required by the Poison Prevention Packaging Act (PPPA). The packaging of the products is not child resistant, posing a risk of chemical burns and irritation to the skin and eyes. In addition, the label on the products violate the Federal Hazardous Substance Act (FHSA) by omitting the word "poison" and other mandatory information on the packaging.
- 2021-05-12CPSCK & M International Inc., d/b/a Wild Republic, of Twinsburg, OhioK & M International Recalls Slap Watches Due to Coin Cell Battery Ingestion and Choking Hazards
The coin cell battery inside the slap watches can fall out, posing battery ingestion and choking hazards to young children.
- 2021-05-06CPSCWalter Kidde Portable Equipment Company Inc., of Mebane, N.C.Kidde Recalls TruSense Smoke and Combination Smoke/Carbon Monoxide Alarms Due to Risk of Failure to Alert Consumers to a Fire
The smoke alarm and the combination smoke/carbon monoxide (CO) alarm can fail to alert consumers to a fire.
- 2021-05-05FDA-FoodChurch & Dwight Co., Inc. OGI Distribution CenterClass IIvitafusion Kids Melatonin 50ct, 4 / 3 PACK 50CT
Potential presence of a metallic mesh material in products.
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