All Recalls

95,075 total recalls in our database

All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and 7XX series) were found to have the potential for abnormal insulin delivery due to changes in air pressure, which can be found during airplane take-off or landing. An unexpected additional dose of insulin, which can occur during take-off, can result in severe hypoglycemia, altered mental status, seizure, coma, or death. An unexpected under-delivery of insulin, which can occur during landing, can result in severe hyperglycemia, dehydration, diabetic ketoacidosis, or death.

Jan 31, 2025 Infusion Pumps Nationwide View Details →
🏥 Medical Devices Class I - Dangerous

All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and 7XX series) were found to have the potential for abnormal insulin delivery due to changes in air pressure, which can be found during airplane take-off or landing. An unexpected additional dose of insulin, which can occur during take-off, can result in severe hypoglycemia, altered mental status, seizure, coma, or death. An unexpected under-delivery of insulin, which can occur during landing, can result in severe hyperglycemia, dehydration, diabetic ketoacidosis, or death.

Jan 31, 2025 Infusion Pumps Nationwide View Details →
🏥 Medical Devices Class I - Dangerous

All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and 7XX series) were found to have the potential for abnormal insulin delivery due to changes in air pressure, which can be found during airplane take-off or landing. An unexpected additional dose of insulin, which can occur during take-off, can result in severe hypoglycemia, altered mental status, seizure, coma, or death. An unexpected under-delivery of insulin, which can occur during landing, can result in severe hyperglycemia, dehydration, diabetic ketoacidosis, or death.

Jan 31, 2025 Infusion Pumps Nationwide View Details →

The initial current in certain chargers may lead to overheating and damage to the power resistors on the Alternating Current (AC) controller during the power-on sequence of the laser system, resulting in the laser system to not power on.

Jan 23, 2025 Other Medical Devices View Details →

Due to an observed trend of neurovascular events

Jan 5, 2025 Surgical Instruments View Details →

Due to the inner diameter of the suction tubing connector being smaller than the suction canister lid port connection. This size difference, combined with the durometer of the plastic material, makes the assembly to a suction canister lid port difficult. This could result in inadequate suction and cause a delay in patient care.

Jan 31, 2025 Other Medical Devices View Details →

Customer-designed sterile surgical procedure packs contain latex components as specified; but, the content label sealed within the transparent sterile pouch contains the symbol for a latex-free product. If users or patients with latex sensitivity come into contact with latex, an allergic reaction may occur.

Feb 10, 2025 Other Medical Devices Nationwide View Details →

All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and 7XX series) were found to have the potential for abnormal insulin delivery due to changes in air pressure, which can be found during airplane take-off or landing. An unexpected additional dose of insulin, which can occur during take-off, can result in severe hypoglycemia, altered mental status, seizure, coma, or death. An unexpected under-delivery of insulin, which can occur during landing, can result in severe hyperglycemia, dehydration, diabetic ketoacidosis, or death.

Jan 31, 2025 Infusion Pumps Nationwide View Details →
🏥 Medical Devices Class I - Dangerous

Tissue approximation straps (zip-ties) have broken before or during implantation so firm developed an interim zip-tie conditioning method submerging zip-ties in 104-degrees F sterile saline solution for 60 min prior to implantation to rehydrate the zip-tie straps. Broken zip-ties not observed during procedure could lead to future hernia recurrence, recurrent surgery to correct a large herniation.

Jan 27, 2025 Other Medical Devices Nationwide View Details →

Patient chart stickers provided inside the packaging may incorrectly identify ET Rigid Abutments as Regular version whereas the actual product is a Mini version; and identify the ET Multi Abutments as Mini version whereas the actual product is a Regular version

Jan 27, 2025 Implants & Prosthetics Nationwide View Details →
🏠 Consumer Products Class I - Dangerous

The metal contact in the switch mechanism of the Recon LT avalanche transceiver can corrode and cause the transceiver to malfunction. If this occurs, the device can turn off and make it impossible to locate a victim in an avalanche, which could result in serious injury or death.

Mar 6, 2025 Other Consumer Products Nationwide View Details →

Lolanta Children's Bathrobes

Unknown Manufacturer

🏠 Consumer Products Class I - Dangerous

The recalled children's bathrobes violate federal flammability regulations for children's sleepwear, posing a risk of burn injuries and death to children.

Mar 6, 2025 Children's Products Nationwide View Details →
🏠 Consumer Products Class II - Moderate

The recalled crib bumpers violate the federal crib bumper ban, posing a deadly suffocation hazard to infants. Padded crib bumpers are banned by the federal Safe Sleep for Babies Act.

Mar 6, 2025 Children's Products Nationwide View Details →

Nuby Stroller Fans

Unknown Manufacturer

🏠 Consumer Products Class III - Low Risk

The stroller fan's housing allows consumers' fingers to contact the fan's blade, posing a laceration injury hazard to small children.

Mar 6, 2025 Furniture Nationwide View Details →
🏠 Consumer Products Class I - Dangerous

The recalled unassembled Deluxe Pit Kit slot cars violate the mandatory federal regulation for magnets because the magnets used to power the car are loose prior to assembly, posing an ingestion hazard to children. Assembled models do not pose this risk and are therefore not subject to this recall. When high-powered magnets are swallowed, the ingested magnets can attract each other, or another metal object, and become lodged in the digestive system. This can result in perforations, twisting and/or blockage of the intestines, infection, blood poisoning and death.

Mar 6, 2025 Electronics Nationwide View Details →

Phosphate Reagent #1 Bottles sold within the Taylor Phosphate Test Kits

Taylor Water Technologies LLC, of Sparks, Maryland

🏠 Consumer Products Class II - Moderate

The recalled Taylor Water Technologies reagent bottles sold with test kits contain sulfuric acid, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act (PPPA). The packaging for the bottle with sulfuric acid is not child resistant, posing a risk of chemical burns to the skin or eyes and internal corrosive burns, if ingested.

Mar 6, 2025 Furniture Nationwide View Details →