Georgia recalls
3,596 federal recalls affecting Georgia in the last 12 months - 234 Georgia-specific plus 3,362 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-01-14FDA-DeviceAVID MedicalClass INationwideDo not use Halyard ORGAN RECOVERY OR PACK
Halyard's ORGAN RECOVERY OR PACK (Kit Code LLOF1000-17) is not suitable for organ transplant procedures. The FDA has classified this as a Class I recall, the most serious type. A total of 52 units were distributed in Florida, Georgia, and Puerto Rico.
- 2026-01-14FDA-DeviceAVID MedicalClass INationwideStop using Halyard ORGAN RECOVERY OR PACK
Halyard ORGAN RECOVERY OR PACK (Kit Code LLOG1000-15) devices have been found to be unsuitable for organ transplant use. The FDA has issued a Class I recall affecting 132 units distributed in Florida, Georgia, and Puerto Rico. No injuries have been reported.
- 2026-01-14FDA-DeviceSiemensClass IINationwideContact Siemens about your LUMINOS X-ray system
Siemens LUMINOS Lotus Max and Luminos dRF Max X-ray systems with software version VF11 may show incorrect collimation (beam positioning) when quickly switching between organ programs. This affects only systems with a bucky wall stand for mobile detectors and no ceiling stand.
- 2026-01-14FDA-DeviceVision RTClass IINationwideCheck AlignRT InBore documentation for laser details
Vision RT identified that instructions for the AlignRT InBore radiation therapy system omitted required information about its six Class 1 lasers and their specifications. The missing details are required by federal laser safety regulations. No injuries have been reported.
- 2026-01-14FDA-FoodSouth Asian FoodClass IStop eating Bengal King Jhal Chanachur
Bengal King Jhal Chanachur food treats (12.34 oz packages) contain peanuts that are not listed on the label. This poses a serious risk to anyone with a peanut allergy. The affected product has lot number HCNCU1205/24 and an expiration date of June 2026.
- 2026-01-14FDA-FoodMAYEJClass IINationwideStop using MAYEJ Italian Parsley
MAYEJ Italian Parsley packaged in 24lb boxes has been recalled due to potential contamination with Cyclospora cayetanensis, a parasite that can cause foodborne illness. About 1,288 boxes were distributed nationwide. No illnesses have been reported so far.
- 2026-01-14FDA-FoodZiyadClass IINationwideStop eating Baraka Gourmet Pastry Kunafe
Ziyad Brothers Importing is recalling Baraka Gourmet Pastry Kunafe (6.7 oz) because it may contain partially hydrogenated oils that are not listed on the label. Partially hydrogenated oils contain trans fats, which are not permitted in food sold in the United States. No injuries have been reported.
- 2026-01-14FDA-FoodZiyadClass IINationwideCheck your Baraka puff pastry for recall
Ziyad Brothers Importing is recalling Baraka French Style Puff Pastry in 1lb and 1.5lb sizes because they may contain partially hydrogenated oils that are not listed on the label. Partially hydrogenated oils are banned in most foods in the United States. No injuries have been reported.
- 2026-01-14FDA-FoodAmbriolaClass IStop using Locatelli Grated Pecorino Romano
Locatelli Grated Pecorino Romano cheese in 8 oz plastic cups has been recalled because it tested positive for Listeria Monocytogenes, a bacteria that can cause serious illness. The affected product was distributed across multiple states in the U.S.
- 2026-01-14FDA-FoodAmbriolaClass IStop using Ambriola Piccante Pecorino Romano cheese
Ambriola Co., Inc. is recalling grated Pecorino Romano cheese in 5 and 10-pound bags because the product tested positive for Listeria monocytogenes, a bacteria that can cause serious illness. The recalled cheese was distributed across multiple states.
- 2026-01-14FDA-FoodAmbriolaClass IDiscard Boar's Head Pecorino Romano Grated cheese
Boar's Head Pecorino Romano Grated cheese in 5-pound bags tested positive for Listeria monocytogenes, a bacterium that can cause serious illness. The affected product was distributed across multiple states. No illnesses have been reported so far.
- 2026-01-14FDA-FoodAmbriolaClass IStop using Sam's Pecorino Romano grated cheese
Sam's Pecorino Romano grated cheese in 1.5 lb plastic bags tested positive for Listeria Monocytogenes, a bacteria that can cause serious illness. The affected product was distributed across multiple states. No illnesses have been reported to date.
- 2026-01-14FDA-FoodAmbriolaClass IDiscard Boar's Head Pecorino Romano cheese
Boar's Head grated Pecorino Romano cheese in 6 oz cups tested positive for Listeria monocytogenes, a bacteria that can cause serious illness. The affected product has lot number 1000572486 and was distributed across multiple states.
- 2026-01-14FDA-FoodAmbriolaClass IStop using Pinna Grated Pecorino Romano
Pinna Grated Pecorino Romano cheese in 10-pound bags tested positive for Listeria Monocytogenes, a bacteria that can cause serious illness. The affected product was distributed across multiple states. No illnesses have been reported so far.
- 2026-01-14FDA-FoodAmbriolaClass IStop using Locatelli Grated Pecorino Romano
Locatelli Grated Pecorino Romano cheese in 5 and 10-pound bags tested positive for Listeria monocytogenes, a bacterium that can cause serious illness. The affected product was distributed across 20 states. No illnesses have been reported so far.
- 2026-01-14FDA-FoodAmbriolaClass IDo not eat Locatelli Grated Pecorino Romano
Locatelli Grated Pecorino Romano cheese in 4 oz and 8 oz plastic cups tested positive for Listeria Monocytogenes, a bacteria that can cause serious illness. The affected product was distributed across multiple U.S. states.
- 2026-01-14FDA-FoodD. Coluccio & SonsClass IIStop eating Sapori Amaretti Almonds cookies
D. Coluccio & Sons Inc. is recalling Sapori Amaretti Almonds 175 g cookies because they contain elevated levels of hydrocyanic acid, a naturally occurring compound in almonds that can be harmful at high levels. Two specific lots are affected with best-before dates of February 5, 2026 and September 3, 2026.
- 2026-01-14FDA-FoodRoviraClass IICheck Tita Crackers Rovira for undeclared dyes
Rovira Biscuit Corporation is recalling Tita Crackers in multiple package sizes because they contain food dyes (FD&C Yellow #6 and FD&C Red 40) that are not listed on the label. These dyes can be a serious concern for people with allergies or sensitivities to artificial colors. No injuries have been reported.
- 2026-01-14FDA-FoodRoviraClass IIStop eating Great Value Vainilla Crackers
Great Value Vainilla Crackers (Galletas Vainilla) contain two food dyes—FD&C Yellow #6 and FD&C Red 40—that are not listed on the package label. People with allergies or sensitivities to these dyes may have an unexpected reaction. No injuries have been reported so far.
- 2026-01-14FDA-FoodRoviraClass IICheck Rovira Vanilla Treats Crackers for dye allergens
Rovira Biscuit Corporation recalled Vanilla Treats Crackers and Mini Vanilla Treats because they contain FD&C Yellow #6 and FD&C Red 40 dyes that are not listed on the package label. People with allergies or sensitivities to these food dyes may have a reaction if they consume the product without knowing these ingredients are present.
- 2026-01-14FDA-FoodRoviraClass IIVanilla Econo, Galletas de Vainilla, 8 paquets per Net Wt. 9.6 oz box (272 g), 6 box per case. UPC 072981005022
Undeclared colors FD&C Yellow #6, and FD&C Red 40
- 2026-01-14FDA-FoodRoviraClass IIStop eating Rovira Tempting Crackers
Rovira Tempting Crackers contain two food colorings—FD&C Yellow #6 and FD&C Red 40—that are not listed on the package label. These dyes can cause allergic reactions in people sensitive to them. No injuries have been reported.
- 2026-01-14FDA-FoodRoviraClass IIDon't eat Rovira 100to en boca crackers
Rovira snack crackers sold in 1.5 oz and 7 oz packages contain two food dyes—FD&C Yellow #6 and FD&C Red 40—that are not listed on the label. People with allergies or sensitivities to these dyes could have a reaction if they consume the product without knowing the dyes are present.
- 2026-01-14FDA-FoodSam Dry Fruits and NutsClass INationwideDon't eat Sam Dry Fruits & Nuts pistachios
Sam Dry Fruits & Nuts Enterprises is recalling whole pistachio meats (Lot #PK00459, 30-lb bags, pack date August 2025) because they may be contaminated with Salmonella, a bacteria that can cause serious illness. This is a Class I recall, the most serious type. No illnesses have been reported so far.
- 2026-01-14FDA-DrugAvKAREClass IINationwideStop using AvKARE Rosuvastatin 10 mg tablets
AvKARE is recalling Rosuvastatin 10 mg tablets (Lot #49124, expiring 12/31/2026) because they don't dissolve properly in the body. This means the medication may not work as intended. No injuries have been reported so far.
- 2026-01-14FDA-DrugMedinaturaClass INationwideStop using ClearLife Allergy Nasal Spray
ClearLife Allergy Nasal Spray Extra Strength has been found to contain yeast, mold, and a bacterium called Achromobacter. The contamination affects all batches still within their expiration date sold nationwide. No injuries have been reported so far.
- 2026-01-14FDA-DrugMedinaturaClass INationwideStop using MediNatura ReBoost Nasal Spray
MediNatura ReBoost Nasal Spray has been found to contain yeast, mold, and a bacterium called Achromobacter. These contaminants should not be in a nasal spray, which is meant to be sterile. The contamination affects all lots currently in use.
- 2026-01-14FDA-DrugSpecGxClass IINationwideCheck your SpecGx pain medication bottle
SpecGx LLC is recalling one lot of oxycodone and acetaminophen tablets (7.5 mg/325 mg) because some tablets may be missing the imprint (identifying mark). This makes it difficult to verify you have the correct medication. No injuries have been reported.
- 2026-01-14FDA-DrugSpecGxClass IINationwideCheck your SpecGx oxycodone tablets
SpecGx LLC is recalling certain bottles of oxycodone and acetaminophen 10mg/325mg tablets because some tablets may be missing the imprint (marking). This could make it difficult to identify the medication. No injuries have been reported.
- 2026-01-14FDA-DrugImprimisClass IINationwideStop using Imprimis Tri-Moxi eye injections
Imprimis NJOF recalled Tri-Moxi+ eye injections because some batches contain glass-like particles. The affected batches (25JAN033A and 25JAN033B) expire in February 2026. No injuries have been reported.
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