Consumer Product Recalls

Hazard: Brakes that are still engaged while driving increase the risk of crash.

Hazard: Use of methanol fuel can damage the pump, causing a fuel leak and increasing the risk of a fire.

Hazard: A battery rupture increases the risk of a fire.

Hazard: Overloading may cause the outer tire to fail, increasing the risk of a crash.

Hazard: A brake chamber air leak may cause the parking brake to partially apply or slow to release, which can overheat the brakes and increase the risk of a fire.

Hazard: An improperly tightened shore power inlet may overheat, increasing the risk of a fire.

Hazard: Oil leaking onto brake components can reduce braking ability and increase the risk of a crash.

Hazard: Small metal pieces can detach from the garlic press, posing a laceration or ingestion hazard to consumers.

Hazard: The recalled children's loungewear violates the flammability standards for children's sleepwear, posing a risk of burn injuries and death to children.

Hazard: The recalled mattresses violate a mandatory flammability standard for mattresses, posing a fire hazard and risk of serious injury or death to consumers.

Hazard: The dual action engagement system on the nailers can malfunction and involuntarily discharge a nail by pulling the trigger alone, posing a laceration hazard to consumers. The nailer should require both the work piece contact element (nose-piece) to be depressed and the trigger to be pulled at the same time in order to discharge a nail.

Hazard: If young children are climbing on the counter or crawling through the opening at the back of the play kitchen, their clothing can get caught on the plastic or metal hooks meant to hold toy kitchen accessories such as play pots and pans, posing a strangulation hazard.

Hazard: The tip of the knife blade doesn't fully fold into the handle, posing a laceration hazard.

Hazard: The recalled magnetic floating stackers toys violate the mandatory standard for toy magnets because they contain magnets that can loosen and detach from the toy, posing an ingestion hazard to children. When high-powered magnets are swallowed, the ingested magnets can attract each other, or other metal objects, and become lodged in the digestive system. This can result in perforations, twisting, and/or blockage of the intestines, blood poisoning and death.

Hazard: The safety bar can detach or break while in use, posing serious fall and injury hazards to consumers.

Hazard: Due to complaints their is the potential that irrigation solution may leaked into the handpiece and battery pack causing it to malfunction.

Hazard: Due to complaints their is the potential that irrigation solution may leaked into the handpiece and battery pack causing it to malfunction.

Hazard: In prior SmartSync application versions, the Abort button stopped the test that was selected. During an induction test, there was a limited window of time for the user to abort a therapy, thereby limiting the user's ability to cancel a high voltage therapy delivery.

Hazard: In prior SmartSync application versions, the Abort button stopped the test that was selected. During an induction test, there was a limited window of time for the user to abort a therapy, thereby limiting the user's ability to cancel a high voltage therapy delivery.

Hazard: Lens blisters may have an incomplete or leaking seal which may render them unsterile.

Hazard: Lens blisters may have an incomplete or leaking seal which may render them unsterile.

Hazard: Due to defects (bubbles/voids) identified during standard finished goods testing

Hazard: Potential for functionality issue that supports the Over labeling feature and could lead to possible false negative results.

Hazard: The firm issued a field safety notice after becoming aware of three lots of products not having quarterly dose audits being completed on time in the first quarter of 2024. Routine lot by lot testing was completed properly however the quarterly dose audit (sampling/testing to monitor the gamma sterilization process and confirm the validated parameters remain effective to assure sterility and bioburden reduction per requirements) was not completed on time.

Hazard: Affected convenience kits contain BD ChloraPrep Clear - 1 mL Applicators, which were recalled by BD due to potential to exhibit an open seal on its packaging. This may constitute a breach to sterility, which may in turn lead to the infection related harms for the patient.

Hazard: Affected convenience kits contain BD ChloraPrep Clear - 1 mL Applicators, which were recalled by BD due to potential to exhibit an open seal on its packaging. This may constitute a breach to sterility, which may in turn lead to the infection related harms for the patient.

Hazard: Affected convenience kits contain BD ChloraPrep Clear - 1 mL Applicators, which were recalled by BD due to potential to exhibit an open seal on its packaging. This may constitute a breach to sterility, which may in turn lead to the infection related harms for the patient.

Hazard: Affected convenience kits contain BD ChloraPrep Clear - 1 mL Applicators, which were recalled by BD due to potential to exhibit an open seal on its packaging. This may constitute a breach to sterility, which may in turn lead to the infection related harms for the patient.

Hazard: A specific lot of bovine serum albumin (BSA) used for manufacturing of coated tubes (CT) that are included in the Estrone RIA kit lots caused different affinity of manufactured coated tubes to patient samples, causing falsely increased assay results for the impacted Estrone RIA kits.

Hazard: Bedside SpO2 Patient Monitoring System alarms not heard/recognized, resulting in: treatment delay, lack of low oxygen saturation response, respiratory failure, arrhythmia. Highlighting operator's manual: 1)For patient Safety don't silence/decrease alarm volume, 2)Sensor off alarm (no perfusion detected) is low priority alarm, 3)Set monitors to Homecare Mode outside of hospital/professional setting