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. 1,116 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
1,116 in last 12 months

Showing 16181–16200 of 53,623 recalls

Medical DeviceJune 9, 2021· Cordis Corporation

Recalled Item: Avanti¿+ Catheter Sheath Introducer - Product Usage: Is indicated for...

The Issue: The product in the packaging is larger (both inner and outer diameter) than...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugJune 9, 2021· Genentech Inc

Recalled Item: Xolair (omalizumab) Injection Recalled by Genentech Inc Due to Failed...

The Issue: Failed Stability Specifications: Out of Specification results of Polysorbate...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 9, 2021· Pfizer Inc.

Recalled Item: Chantix (varenicline)Tablets Recalled by Pfizer Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: Presence of the N-nitroso-varenicline impurity above FDAs...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 9, 2021· Pfizer Inc.

Recalled Item: Chantix (varenicline) tablets Recalled by Pfizer Inc. Due to CGMP...

The Issue: CGMP Deviations: Presence of the N-nitroso-varenicline impurity above FDAs...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 9, 2021· Pfizer Inc.

Recalled Item: Chantix (varenicline) tablets Recalled by Pfizer Inc. Due to CGMP...

The Issue: CGMP Deviations: Presence of the N-nitroso-varenicline impurity above FDA s...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 8, 2021· Bausch Health Companies, Inc.

Recalled Item: Mephyton (Phytonadione) 5 mg tablets Recalled by Bausch Health Companies,...

The Issue: Failed Impurities/Degradation Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugJune 8, 2021· Bausch Health Companies, Inc.

Recalled Item: Phytonadione Tablets Recalled by Bausch Health Companies, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceJune 8, 2021· Philips North America Llc

Recalled Item: 728333 Spectral CT 7500 -Computed Tomography X-ray system Recalled by...

The Issue: When setting patient weight unit preferences to pounds, SynchRight P3T...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2021· Philips North America Llc

Recalled Item: 728332 IQon Spectral CT-Computed Tomography X-ray system Recalled by Philips...

The Issue: When setting patient weight unit preferences to pounds, SynchRight P3T...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2021· Philips North America Llc

Recalled Item: 728306 Brilliance iCT-Computed Tomography X-ray systems 728305 Brilliance...

The Issue: When setting patient weight unit preferences to pounds, SynchRight P3T...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2021· Philips North America Llc

Recalled Item: 728327 Ingenuity CT Upgrades-Computed Tomography X-ray system Recalled by...

The Issue: When setting patient weight unit preferences to pounds, SynchRight P3T...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2021· Philips North America Llc

Recalled Item: Model 728321/728323 CT5000 Ingenuity Plus/Pro/Premium-Computed Tomography...

The Issue: When setting patient weight unit preferences to pounds, SynchRight P3T...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodJune 8, 2021· Beechnut Nutrition

Recalled Item: Beech-Nut brand Single Grain Rice Baby Cereal Recalled by Beechnut Nutrition...

The Issue: Product may contain elevated levels of inorganic arsenic (above 100ppb)

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 7, 2021· Medtronic Vascular, Inc.

Recalled Item: Medtronic Endurant IIs Stent Graft System Medtronic Endurant IIs Stent...

The Issue: During product complaint investigation, it was determined that during stent...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2021· Medtronic Vascular, Inc.

Recalled Item: Endurant II/Endurant IIs Stent Graft System: Medtronic Endurant II Stent...

The Issue: During stent graft deployment, the radiopaque (RO) marker bond detached from...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2021· BioFire Diagnostics, LLC

Recalled Item: FilmArray Pneumonia Panel (Pneumo) Part Numbers: Part No: RFIT-ASY-0144 /...

The Issue: Due to real-time stability study failures resulting in increase rate of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2021· BioFire Diagnostics, LLC

Recalled Item: FilmArray Pneumonia Panel plus (Pneumoplus) Part Numbers: Part No:...

The Issue: Due to real-time stability study failures resulting in increase rate of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2021· Simpleware Product Group, SYNOPSYS NORTHERN EUROPE

Recalled Item: Simpleware ScanIP medical software. For transfer of imaging information from...

The Issue: A issue (bug) has been identified with the interface and image software...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2021· Simpleware Product Group, SYNOPSYS NORTHERN EUROPE

Recalled Item: Simpleware ScanIP software. For transfer of imaging information from a...

The Issue: A issue (bug) has been identified with the interface and image software...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2021· Eight Medical International BV

Recalled Item: Recirculator 8.0s Disposable Lavage Kit (product code number 8100) Recalled...

The Issue: The patient may be exposed to potential aluminum ion release during warming...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing