Recalls affecting Rhode Island
Notices that name Rhode Island in their distribution area, plus every nationwide recall — nationwide recalls reach Rhode Island too.
-
Class I · 1+ years ago
DermaRite Industries, LLC KleenFoam, Antimicrobial Foam Soap with Aloe Vera recall: Microbial Contamination of Non-Sterile Drug Product: The products were found
Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.
-
Class II · 1+ years ago
Amneal Pharmaceuticals, LLC Sulfamethoxazole and Trimethoprim Tablets, USP 800mg/160mg recall: Presence of a foreign substance.A specific lot of auxiliary polyester coil
Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging was detected with presence of a micro-organism…
-
Class I · 1+ years ago
DermaRite Industries, LLC DermaKleen, Health Care Antiseptic Lotion Soap with Vitamin recall: Microbial Contamination of Non-Sterile Drug Product: The products were found
Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.
-
Class II · 1+ years ago
Amneal Pharmaceuticals, LLC chlorproMazine Hydrochloride Tablets, USP recall: Presence of a foreign substance.A specific lot of auxiliary polyester coil
Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging was detected with presence of a micro-organism…
-
Class II · 1+ years ago
Amneal Pharmaceuticals, LLC chlorproMazine Hydrochloride Tablets, USP recall: Presence of a foreign substance.A specific lot of auxiliary polyester coil
Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging was detected with presence of a micro-organism…
-
Class II · 1+ years ago
Amneal Pharmaceuticals, LLC chlorproMazine Hydrochloride Tablets, USP recall: Presence of a foreign substance.A specific lot of auxiliary polyester coil
Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging was detected with presence of a micro-organism…
-
Class III · 1+ years ago
Fluorescein 2% Ophth, 3 ML, Boothwyn Pharmacy, 800-476-7496 recall: Subpotent Drug
Subpotent Drug
-
Class I · 1+ years ago
DermaRite Industries, LLC DermaSarra, External Analgesic, 222 mL per bottle recall: Microbial Contamination of Non-Sterile Drug Product: The products were found
Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.
-
Class I · 1+ years ago
DermaRite Industries, LLC PeriGiene, Health Care Antiseptic, 222 mL per bottle recall: Microbial Contamination of Non-Sterile Drug Product: The products were found
Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.
-
Class II · 1+ years ago
Semaglutide, 2.5 mg/mL injection, 0.8 mL, Boothwyn Pharmacy recall: Subpotent Drug
Subpotent Drug
-
NHTSA safety recall · 1+ years ago
Rivian Automotive R1S and R1T recall: 18.30. The Hands-Free Highway Assist (HWA) software may fail to correctly
18.30. The Hands-Free Highway Assist (HWA) software may fail to correctly identify a lead vehicle.
-
NHTSA safety recall · 1+ years ago
Honda 2020-2022 and CRF1100 Africa Twin recall: The left handlebar switch harness may corrode due to oxidation
The left handlebar switch harness may corrode due to oxidation, resulting in the loss of horn function or the ability to switch the headlight from…
-
NHTSA safety recall · 1+ years ago
Honda Acura RDX recall: The software for the electric power steering (EPS) assist
The software for the electric power steering (EPS) assist may not be calibrated properly, which can cause the EPS system to enter a failsafe mode…
-
NHTSA safety recall · 1+ years ago
Toyota bZ4X, Lexus RZ and and Subaru Solterra recall: During certain HVAC system faults, such as electrical compressor failure
During certain HVAC system faults, such as electrical compressor failure, the defroster and defogger system may become inoperative.
-
NHTSA safety recall · 1+ years ago
Chrysler Jeep Wagoneer S recall: The vehicles are equipped with an incorrect cross car beam in the instrument
The vehicles are equipped with an incorrect cross car beam in the instrument panel. As such, these vehicles fail to comply with the requirements of…
-
NHTSA safety recall · 1+ years ago
Chrysler recall: A software error within the hybrid control processor may result in a loss
A software error within the hybrid control processor may result in a loss of drive power.
-
NHTSA safety recall · 1+ years ago
Chrysler Dodge Charger and Jeep Wagoneer S electric recall: An incorrectly installed spring may cause the loss of the park function
An incorrectly installed spring may cause the loss of the park function when the vehicle’s gear selector is placed in the park (P) position, which…
-
NHTSA safety recall · 1+ years ago
Chrysler Pacifica and Voyager recall: The right and left side curtain air bags may have insufficient pressure
The right and left side curtain air bags may have insufficient pressure retention from improperly sealed seams. As such, these vehicles fail to…
-
Highest risk · 1+ years ago
StopBox USA AR-15 Chamber Lock Pros recall: Risk of Serious Injury and Death
Risk of Serious Injury and Death
-
Highest risk · 1+ years ago
Makita U.S.A., Inc. Cordless Grease Guns and Grease Gun Hoses recall: Laceration Hazard
Laceration Hazard
-
Class III · 1+ years ago
Philips Ultrasound, Inc X3-1 Transducer Probe recall: To provide clarification and labelling to define the useful life
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
-
Class II · 1+ years ago
CareFusion 303, Inc. BD Pyxis Product Name / UDI-DI code / recall: Antivirus software was not consistently installed on impacted devices during
Antivirus software was not consistently installed on impacted devices during the implementation process.
-
Class III · 1+ years ago
Philips Ultrasound, Inc S7-2t Transducer Probe recall: To provide clarification and labelling to define the useful life
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
-
Class III · 1+ years ago
Philips Ultrasound, Inc S12-4 Transducer Probe recall: To provide clarification and labelling to define the useful life
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.