State
73,584 recalls have nationwide distribution and so reach Georgia. 9,624 additional recalls listed Georgia specifically in their distribution scope.
Of the 9,624 recalls naming Georgia we have scored against our rubric, 1,474 (15%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,561 (27%) are Severe.
Which agencies issued them
These figures cover only the 9,624 recalls whose distribution notice names Georgia specifically. The 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
General Motors is recalling 2021-2022 Chevrolet Silverado and GMC Sierra pickup trucks due to brake modulator bolts that may fail to seal properly. Water intrusion can cause electrical short circuits, creating a fire risk.
Macy's is recalling Martha Stewart Collection Oil & Vinegar Cruets because the glass portion can break during use, causing cuts. Six incidents have been reported, including three lacerations with two requiring stitches.
Olympus is recalling the EVIS EXERA BF-XT160 bronchofibervideoscope due to a missing gluing step in manufacturing. The affected devices may develop leaks in the insertion tube, posing an infection control risk.
Venom Motorsports is recalling about 500 youth all-terrain vehicles (ATVs) because they do not meet mandatory safety requirements, including speed restrictions, and were distributed without CPSC approval. The recalled ATVs pose a risk of serious injury or death.
The Sight OLO-E1/U1 diagnostic device software contains a labeling discrepancy: the operator's manual and software present different adult CBC reference ranges, potentially affecting the interpretation of diagnostic results.
C.R. Bard Inc is recalling a Foley catheter tray due to potential packaging defects that may compromise the sterile barrier. Approximately 1,710 units were distributed nationwide.
Aesculap Implant Systems is recalling Univation X System knee implants because they may loosen, potentially requiring additional surgery. The recall affects devices distributed nationwide.
C.R. Bard is recalling 5,950 SureStep Foley Tray kits nationwide due to potential packaging defects that may impact the sterile barrier.
GE Healthcare's Centricity PACS-IW system experiences image acquisition and synchronization failures that could impair the display of medical images. The software malfunction affects 392 devices globally.
Aesculap Implant Systems is recalling Univation X System knee implant devices (all lots, nationwide) because the implants may loosen, potentially requiring revision surgery. No injuries have been reported.
Greiner Bio-One is recalling 956,400 VACUETTE coagulation blood collection tubes that may clot due to anticoagulant variation or low vacuum.
C.R. Bard is recalling 2,660 units of SureStep Foley Catheter Trays nationwide due to potential packaging defects that may impact the sterile barrier.
C.R. Bard is recalling SureStep Foley Tray units due to potential packaging defects that may compromise the sterile barrier. The recalled product was distributed nationwide in the United States.
Aurobindo Pharma USA Inc. is recalling Metoprolol Tartrate 100 mg tablets due to the presence of metal wire found in at least one tablet. The FDA classified this as a Class II recall affecting 2,820 bottles distributed nationwide.
Jayco is recalling certain 2019-2021 Entegra and Jayco Class A motorhomes because the instrument cluster may go blank while driving, potentially hiding speed and warning lights.
C.R. Bard Inc is recalling SureStep Foley Trays (Catalog A902616) due to packaging defects that may compromise the sterile barrier. Affected units were distributed nationwide.
Argon Medical Devices is recalling the Scorpion Portal Vein Access Set due to design changes that have caused the sheaths to crack or break at the tips. The affected product was distributed in the United States.
Ad-Tech Lightweight CABRIO Cables with incorrect labels are being recalled. Mislabeling could cause product misidentification affecting proper use in clinical monitoring applications.
Pfizer is recalling certain lots of Chantix (varenicline tartrate) 0.5mg tablets nationwide due to the presence of N-nitroso-varenicline impurity above FDA's acceptable interim intake limit.
Ad-Tech Medical recalled its Lightweight TECH ATTACH Cable due to incorrect labels on affected units. The cables are designed to connect electrodes to third-party monitors and stimulators.
Sysco Atlanta is recalling Imperial Fresh diced Roma tomatoes due to improper temperature storage that may have made the product unsafe to consume.
Sysco Atlanta is recalling Minor's Seafood Base No MSG GF shipped between July and August 2021 to Georgia, North Carolina, and Tennessee because the product was not held at an appropriate temperature and may be unsafe to consume.
Sysco Atlanta is recalling Sunny Creek Sprout Bean Fresh in 1/5 lb plastic bags due to improper temperature storage that could make the food unsafe to consume.
Sysco Atlanta is recalling Ken's Steakhouse Asian Sesame Dressing after the product was not held at appropriate temperatures. The improper storage conditions could make the food unsafe to consume.
American Health Packaging is recalling Sirolimus 1 mg tablets (Lot #1000789, expiring 10/31/2022) distributed nationwide because they failed impurities and degradation specifications.