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Consumer Product Recalls

127,277 recalls from the U.S. Consumer Product Safety Commission, newest first.

June 5, 2025AppliancesCPSC
Midea Recalls About 1.7 Million U and U+ Window Air Conditioners Due to Risk of Mold Exposure
Hazard: Pooled water in the air conditioners can fail to drain quickly enough, which can lead to mold growth. Mold exposure poses risks of respiratory issues or other infections to some consumers.
June 5, 2025Bikes & Recreational VehiclesCPSC
Specialized Bicycle Components Recalls Globe-Branded Haul ST and LT E-Bikes Due to Fall Hazard
Hazard: When the lower portion of the e-bike's telescopic seat post is fully extended, the seat post can break, posing a fall hazard.
June 5, 2025Children's ProductsCPSC
Funlio Convertible High Chairs Recalled Due to Risk of Serious Injury or Death from Fall and Entrapment Hazards; Violation of Federal Standards for High Chairs; Sold by Ecogoods
Hazard: The recalled high chairs pose a deadly entrapment hazard because the opening between the seat and tray is large enough that a child can become entrapped in it. In addition, the child restraint system can fail, posing a fall hazard. These are violations of the federal standards for high chairs.
June 5, 2025OtherCPSC
Lutron Recalls Power Interfaces for LED Tape Lights Due to Shock Hazard
Hazard: The power interface can fail during a significant power surge (e.g., lightning strike), posing a shock hazard to consumers if they touch the LED tape lights.
June 5, 2025OtherCPSC
Portable Hook-On Chairs Recalled Due to Risk of Serious Injury or Death from Fall Hazard; Violation of the Federal Standard for Portable Hook-On Chairs; Sold Exclusively on Amazon.com by Ravmix
Hazard: The recalled portable hook-on chair poses a deadly fall hazard because the crotch restraint can be removed without the use of a tool and infants can fall through an opening, which is a violation of the federal standard for portable hook-on chairs.
June 5, 2025Children's ProductsCPSC
ZHORANGE Portable Bassinets Recalled Due to Risk of Serious Injury or Death from Fall Hazard; Violation of Federal Standard for Infant Sleep Products; Sold on Amazon.com by DFD Trading
Hazard: The recalled portable bassinets violate the federal safety standard for Infant Sleep Products because the sides are too low to contain the infant and the portable bassinets do not have a stand, posing a fall hazard. These violations create an unsafe sleeping environment for infants.
June 5, 2025ToysCPSC
Hobby Toy Hammer Ball Sets Recalled Due to Risk of Serious Injury or Death from Choking Hazard; Violation of Federal Regulation for Toys with Small Balls; Sold Exclusively on Amazon.com by Shantou Haochengheng Technology
Hazard: The toy sets contain small balls that violate regulations for toys intended for children under three years of age because they are a choking hazard and can cause serious injury or death.
June 5, 2025AppliancesCPSC
Rinnai America Recalls Boilers Due to Carbon Monoxide (CO) Poisoning Hazard
Hazard: The boiler door can fail to seal properly due to incorrect screws, allowing carbon monoxide (CO) gases to escape, posing a carbon monoxide poisoning hazard.
June 5, 2025Children's ProductsCPSC
ZRWD Infant Swings Recalled Due to Risk of Serious Injury or Death from Suffocation Hazard; Multiple Federal Safety Violations; Sold Exclusively on Amazon.com by ZRWD
Hazard: The swings pose a deadly suffocation risk because they were marketed for infant sleep and they have an incline angle greater than 10 degrees, in violation of the CPSC's Infant Sleep Products Standard and Safe Sleep for Babies Act. The swings also fail to meet mandatory warning requirements under the swing standard. In addition, the remote control for the swing contains a lithium coin battery and the products are missing the required warnings and instructions for consumer products containing button cell and coin batteries under Reese's Law. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.
June 5, 2025AppliancesCPSC
Johnson Health Tech Trading Recalls BowFlex Adjustable Dumbbells Due to Impact Hazard, Including 3.7 Million Sold by Nautilus Inc.
Hazard: The weight plates can dislodge from the handle during use, posing an impact hazard.
June 4, 2025Medical DevicesFDA
Onkos Surgical, Inc. recalls Male-Female Midsection with the following sizes and model numbers. a. Male-Female Midsection, 40mm, 1 EACH; Model Num
Hazard: Potential for breach of Tyvek seals.
June 4, 2025Medical DevicesFDA
Onkos Surgical, Inc. recalls Ethos Collar Stem, Cemented, Fluted, 100MM, 1 EACH. Model Numbers: HC-09100-03M, HC-10100-03M, HC-11120-03M, HC-13120-03
Hazard: Potential for breach of Tyvek seals.
June 4, 2025Medical DevicesFDA
Onkos Surgical, Inc. recalls Segmental Stem, Canal Filling, Bowed 152MM, 1 EACH. Model Numbers: FB-11152-03M, FB-12152-03M, FB-13152-03M, FB-14152-03
Hazard: Potential for breach of Tyvek seals.
June 4, 2025Medical DevicesFDA
Onkos Surgical, Inc. recalls Segmental Stem, Canal Filling, Straight, 120MM, 1 EACH. Model Numbers: FS-11120-03M, FS-12120-03M, FS-13120-03M, FS-1412
Hazard: Potential for breach of Tyvek seals.
June 4, 2025Medical DevicesFDA
Onkos Surgical, Inc. recalls Segmental Stem, Cemented, Bowed, 152MM, 1 EACH. Model Numbers: CB-11152-03M, CB-13152-03M, CB-15152-03M, CB-17152-03M.
Hazard: Potential for breach of Tyvek seals.
June 4, 2025Medical DevicesFDA
Onkos Surgical, Inc. recalls a. Segmental Stem, Cemented, Straight, 100MM, 1 EACH; Model Numbers: CS-09100-03M, CS-10100-03M. b. Segmental Stem, C
Hazard: Potential for breach of Tyvek seals.
June 4, 2025Medical DevicesFDA
BioFire Diagnostics, LLC recalls BioFire Respiratory Panel 2.1 plus Kit, REF: 423740, For Filmarray systems
Hazard: Due to manufacturing error, respiratory panel may result in elevated control failures and/or false negative results.
June 4, 2025Medical DevicesFDA
Ortho-Clinical Diagnostics, Inc. recalls VITROS Chemistry Products CRP Slides. One sales unit contains 5 cartridges, of 18 slides per cartridge, for a total of 9
Hazard: Product was incorrectly assigned GEN 88 instead of GEN 83 on product carton, foil wrapper, and cartridge (cart) label.
June 4, 2025Medical DevicesFDA
Cardinal Health 200, LLC recalls Catalog No. 8888160648; Umbilical Vessel Catheter 5 French triple lumen
Hazard: Packaging defect may compromise sterility of the product. Use of a non-sterile product on the patient could lead to infection in neonates.
June 4, 2025Medical DevicesFDA
Cardinal Health 200, LLC recalls Catalog No. 8888160556; Umbilical Vessel Catheter 5 French dual lumen
Hazard: Packaging defect may compromise sterility of the product. Use of a non-sterile product on the patient could lead to infection in neonates.
June 4, 2025Medical DevicesFDA
Cardinal Health 200, LLC recalls Catalog No. 8888160341; Umbilical Vessel Catheter 5 French single lumen
Hazard: Packaging defect may compromise sterility of the product. Use of a non-sterile product on the patient could lead to infection in neonates.
June 4, 2025Medical DevicesFDA
Cardinal Health 200, LLC recalls Catalog No. 8888160333; Umbilical Vessel Catheter 3.5 French single lumen
Hazard: Packaging defect may compromise sterility of the product. Use of a non-sterile product on the patient could lead to infection in neonates.
June 4, 2025Medical DevicesFDA
Cardinal Health 200, LLC recalls Catalog No. 8888160325; Umbilical Vessel Catheter 2.5 French single lumen
Hazard: Packaging defect may compromise sterility of the product. Use of a non-sterile product on the patient could lead to infection in neonates.
June 4, 2025Medical DevicesFDA
Cardinal Health 200, LLC recalls Catalog No. 8888160119; Umbilical Vessel Catheter Insertion Tray with 2.5 and 5 French UVCs
Hazard: Packaging defect may compromise sterility of the product. Use of a non-sterile product on the patient could lead to infection in neonates.
June 4, 2025Medical DevicesFDA
NxStage Medical Inc recalls NxStage PureFlow-B Solution. Catalog numbers: RFP-400, RFP-401, RFP-402, RFP-403, RFP-404, RFP-406, RFP-453, RFP-454, RF
Hazard: Potential for the perimeter seal on the small chamber of the two-chamber bag to fail causing the electrolyte fluid to splash into the face of the user when attempting to open the peel seam to mix the two chambers prior to treatment.
June 4, 2025Medical DevicesFDA
Straumann USA LLC recalls GM Helix Acqua Implant, Article Number: 140.985
Hazard: It is possible that a package labelled as an 11.5 mm implant may contain a 13 mm implant instead.
June 4, 2025Medical DevicesFDA
Straumann USA LLC recalls GM Helix Acqua Implant, Article Number: 140.984
Hazard: It is possible that a package labelled as an 11.5 mm implant may contain a 13 mm implant instead.
June 4, 2025Medical DevicesFDA
Straumann USA LLC recalls Plus Initial Drill, Article Number: 103.170;
Hazard: The referred batch was produced without the laser engraving of 7 mm.
June 4, 2025Medical DevicesFDA
Pro-Med Instruments Gmbh recalls DORO¿ Easy-Connect Navigation Adaptor; BRAINLAB (item No. 1204.002)
Hazard: Potential of compromised compatibility resulting in influence on the positioning of the reference array and an influence of the function of the navigation system cannot be excluded.
June 4, 2025Medical DevicesFDA
Ultra Clean Systems, Inc. recalls Ultrasonic Cleaning Systems Triton 36 Model Number 6003000804 Triton 72 Model Number 6003000805 Ultrasonic cleaning
Hazard: During routine preventative maintenance checks, it was revealed that carbon filter sensors were breaking down due to electrochemical degradation.