Product recalls in United States
Every recall and safety alert published in United States that we collect, newest first: food, vehicles, children's products, electrical goods, medicines and more.
3,853 recalls, newest first · Checked 3 minutes ago
United States
Joolz Recalls Aer2 Car Seat Adapters for Strollers Due to Risk of Serious Injury or Death from Suffocation and Fall Hazards; Violates Mandatory Standard for Infant Sleep Products
The baby loungers violate the mandatory standard for Infant Sleep Products because the sides are shorter than the minimum side height limit to secure the infant; the…
Joolz Recalls Aer2 Car Seat Adapters for Strollers Due to Risk of Serious Injury from Fall Hazard
The recalled car seat adapters can fail to properly attach to the stroller, which may allow the car seat to fall, posing a risk of serious injury from a fall hazard.
GOPO Toys Recalls Pull String Teething Toys Due to Risk of Serious Injury or Death from Choking; Violate Mandatory Standard for Toys
The recalled teething toys violate the mandatory standard for toys because the silicone strings are smaller and longer than permitted.
Bada Boom Fireworks Recalls Pyro Diablo "Diablo Rising" Fireworks Due to Risk of Serious Injury or Death from Explosion and Burn Hazards; Violate Fireworks Ban
The recalled fireworks violate the ban for aerial fireworks devices intended to produce audible effects because they have a pyrotechnic composition that exceeds the…
BABESIDE Doll and Stroller Children's Toys Recalled Due to Risk of Serious Injury or Death from Choking Hazard; Violate Small Parts Ban; Sold on Amazon by HYBDOLLS
The recalled toys violate the small parts ban because they are intended for children under three and the small pacifier poses a deadly choking hazard to young children.
Arizer Solo III Portable Vaporizers Recalled Due to Fire and Burn Hazards; Risk of Serious Injury or Death; Imported by 7111495 Canada
The pajama sets violate the mandatory safety standards for children's sleepwear, posing a risk of serious injury or death to children from burns.Berlin Heart GMBH recalls EXCOR Pediatric Ventricular Assist Device
Blood pump inner package expiration date does not match the outer-correct expiration date, which may lead to delays in surgical procedures.Abbott Medical recalls Merlin" Patient Care System
Software malfunction may occur during pacing capture threshold test of pacemaker resulting in programmer not successfully communicating the command to terminate the test.Medartis AG recalls Medartis APTUS
The cannulation of the CCS screw is not centered.Inter-Med Llc recalls Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit
Some units of Aluminum Chloride Gel contain the package insert for Ferric Sulfate Gel.DT MedTech, LLC recalls Hintermann Series Talar Implant
Through customer complaints, the ankle replacement system was found to contain incorrect devices: Left implant packaging and labeling bears a right implant device.Boston Scientific Corporation recalls Orca Single Use Air/Water and Suction Valves
Boston Scientific is initiating a medical device removal of Orca Sterile, Single Use Air/Water and Suction Valves due to a higher than anticipated occurrence of the…Philips North America Llc recalls DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035.
System was delivered without the required Seismic kit for Wall Stand VS2, which is designed to prevent damage and ensure stability of the Wall Stand VS2 during seismic…Fresenius Medical Care Holdings, Inc. recalls Bicarby" Dialysate
Given the increased number of leaks reported by users, it was determined to be the appropriate course of action to notify users of the potential for the occurrence of…ICU Medical, Inc. recalls Plum Solo Precision IV Pump and 2 more products
Under certain conditions, the pump may not display a soft limit alert, and will not notify the clinician of a soft limit violation before confirming and starting…Siemens Healthcare Diagnostics, Inc. recalls Siemens Dimension Tacrolimus Flex Reagent Cartridge
A potential positive bias in quality control (QC) and patient sample results in three lots of the Dimension Tacrolimus (TAC) Flex reagent cartridge.Elekta, Inc. recalls MOSAIQ Oncology Information System
Software may fail to load adapted baseline shift plan during treatment delivery when a communication error occurs.HF Acquisition Co LLC recalls Brand Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE and 1 more products
Due to incorrect incubation process being performed on product.The Binding Site Group, Ltd. recalls Brand Name: EXENT Analyser Product Name: EXENT Analyser Model/Catalog Number: IE800.A…
It was reported that plates 2 and 3 were marked as passed , although it appeared that QC had not been performed on these plates, despite samples being measured.AVID Medical, Inc. recalls Halyard and 3 more products
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.Fresh Roast Systems Inc recalls Fresh Roast Systems ColorTrack. Model Name: ColorTrack. Model Number: BENCH R-100
A defect has been identified in the manufacture of the Fresh Roast Systems ColorTrack instrument model number BENCH R-100 which could under very rare specific misuse…D.O.R.C. Dutch Opthalmic Research Center Intl B.V. recalls TDC VELOCE" and 2 more products
An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use.Sagemax Bioceramics, Inc. recalls NexxZr T Multi A3.5 W98-16mm
Yttrium-stabilized zirconium oxide discs for fixed all-ceramic dental restorations may have reduced or missing dentin layer and when used clinically in the patient's…A little guidance
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What to do if something you own is recalled
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