Product Recalls in Georgia
Product recalls affecting Georgia — including food, drugs, consumer products, medical devices, and vehicles distributed to Georgia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,643 recalls have been distributed to Georgia in the last 12 months.
Showing 25741–25760 of 29,505 recalls
Recalled Item: PENTARAY NAV High-Density Mapping Catheter and PENTARAY NAV ECO Catheter...
The Issue: Biosense Webster is recalling the PentaRay Nav Catheter because it has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS TT4 Calibrator For the quantitative measurement of total thyroxine...
The Issue: Total T4 Calibrators and Reagent Packs may have calibration failures or low...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proceed Surgical Mesh Recalled by Ethicon, Inc. Due to The possibility...
The Issue: The possibility exists that an incomplete seal on the packaging compromised...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FreeStyle Flash Blood Glucose Monitors System. Meter made in China Recalled...
The Issue: Abbott Diabetes Care has identified through internal testing and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heparin I.V. Flush Syringe is available is pre-filled polypropylene syringes...
The Issue: The bar code that is printed on the Master Carton label does not correspond...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FreeStyle Blood Glucose Monitors System. For in vitro diagnostic use...
The Issue: Abbott Diabetes Care has identified through internal testing and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartStart MRx Defibrillator/Monitor M3538A Lithium Ion Batteries Revision J...
The Issue: Philips HeartStart MRx Monitor/Defibrillator, when operating on battery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartStart MRx Monitor/Defibrillator Recalled by Philips Medical Systems,...
The Issue: A component of the MRx Processor Board may be susceptible to damage from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Vancomycin 30 mcg Recalled by Remel Inc Due to Some of the discs may...
The Issue: Some of the discs may not be impregnated with the antibiotic.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur XP Immunoassay system Recalled by Siemens Healthcare...
The Issue: Instrument Cover Gas Spring failures. Over time, the gas spring may lose its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Recalled by Philips Medical...
The Issue: ECG trunk cable and connector block of the MRx could be susceptible to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Model numbers: M3535A Recalled...
The Issue: MRx may display a Red X in the Ready For Use (RFU) indicator during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GemStar Docking Station Recalled by Hospira Inc. Due to There are two...
The Issue: There are two situations that may occur when using the GemStar Docking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Models: M3535A and M3536A with...
The Issue: When the HeartStart MRx.is used with the Q-CPR Meter in defibrillation mode,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XiO RPT System The XiO RTP System is used to Recalled by Elekta, Inc. Due to...
The Issue: Dose and Monitor Unit values are not computed correctly when Elekta...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RaySearch Ray Station Radiation Therapy Treatment Planning System Recalled...
The Issue: RaySearch Laboratories has recalled "RaySearch Ray Station 2.0, 2.5, 3.0,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Device Name: ABX PENTRA ML Model/Part #(s): A11A01652 Lot/Serial #(s):...
The Issue: HORIBA Medical initiated this recall of all software versions of ABX PENTRA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart XL Recalled by Philips Medical Systems, Inc. Due to...
The Issue: Philips HeartStart XL may experience a power board failure causing failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima CT580/Discovery CT590RT scanners running software...
The Issue: GE Healthcare has recently become aware of a potential safety issue due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spacelabs Healthcare G2 Clinical Access Mislabeled CDs for PN: 063-1829-11...
The Issue: Spacelabs has voluntarily recalled G2 Clinical Access Software CD because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.