Product Recalls in Rhode Island
Product recalls affecting Rhode Island — including food, drugs, consumer products, medical devices, and vehicles distributed to Rhode Island. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,401 recalls have been distributed to Rhode Island in the last 12 months.
Showing 18481–18500 of 47,970 recalls
Recalled Item: TandemHeart pump is assembled into kits: TandemLung Kit - DL31 Recalled by...
The Issue: Failure to prime due to an assembly error
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TandemHeart pump is assembled into kits: TandemHeart Kit - TS62/A17 Recalled...
The Issue: Failure to prime due to an assembly error
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TandemHeart Pump Kit Recalled by Cardiac Assist, Inc Due to Failure to prime...
The Issue: Failure to prime due to an assembly error
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TandemHeart pump is assembled into kits: ProtekDuo Kit - DL29 Recalled by...
The Issue: Failure to prime due to an assembly error
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TandemHeart pump is assembled into kits: ProtekDuo Kit - DL3 Recalled by...
The Issue: Failure to prime due to an assembly error
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TandemHeart pump is assembled into kits: TandemLife Kit Product: 5740-0000...
The Issue: Failure to prime due to an assembly error
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TandemHeart pump is assembled into kits: ProtekDuo Kit - DL31 RD Recalled by...
The Issue: Failure to prime due to an assembly error
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TandemHeart pump is assembled into kits: TandemHeart Kit - TS62/A15 Recalled...
The Issue: Failure to prime due to an assembly error
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRx4841A 1.4 GHz IntelliVue Tele TRX Recalled by Philips North America, LLC...
The Issue: The ECG signal from patients being monitored using a Philips TRx4841A and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRx4851A 2.4 GHz IntelliVue Tele TRX Recalled by Philips North America, LLC...
The Issue: The ECG signal from patients being monitored using a Philips TRx4841A and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phillips Azurion 7 M20 Recalled by Philips North America, LLC Due to No...
The Issue: No torque was specified for the four screws that connect the gearbox and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEM Microvascular Anastomotic Coupler Devices - Product Usage: s intended...
The Issue: The Coupler size labeling of the outer tray may not match the Couper size...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEM Microvascular Anastomotic Coupler Devices s intended to be used Recalled...
The Issue: The Coupler size labeling of the outer tray may not match the Couper size...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEM Microvascular Anastomotic Coupler Devices - Product Usage: is intended...
The Issue: The Coupler size labeling of the outer tray may not match the Couper size...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips V60 Ventilators with Power Management PCBA part number 1055906...
The Issue: Solder connection failure on Power Management printed circuit board assembly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: natus newborn care Olympic Brainz Monitor Recalled by Natus Neurology DBA...
The Issue: The OBM system functional test (impedance and noise) was not carried out on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PrediniSONE Tablets Recalled by Par Pharmaceutical Inc. Due to Labeling:...
The Issue: Labeling: Incorrect or Missing Exp Date - An incorrect expiration date has...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: STA - Deficient VIII Recalled by Diagnostica Stago, Inc. Due to A risk of...
The Issue: A risk of sample-to-sample cross-contamination of Emicizumab for factor VIII...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation standalone software treatment planning system Recalled by...
The Issue: Due to physical limitations of the treatment machine, the maximum field...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PEPPERMINT LIP MOISTURIZER (oxybenzone (4%) and Octinoxate (7%) SPF 15...
The Issue: Superpotent drug: This lot of SPF containing lip balm contains up to 150% of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.