State

Georgia product recalls

73,817 recalls have nationwide distribution and so reach Georgia. 9,635 additional recalls listed Georgia specifically in their distribution scope.

What the numbers show

Total: 9,635
Critical: 1,471
Severe: 2,567
Most recent: 2026-11-04

Of the 9,635 recalls naming Georgia we have scored against our rubric, 1,471 (15%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,567 (27%) are Severe.

Which agencies issued them

These figures cover only the 9,635 recalls whose distribution notice names Georgia specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

49901–49925 of 83452

SevereFDA (Drugs)·D-0638-2017·2017-04-12
Hospira Recalls Vancomycin Hydrochloride Injection Due to Particulate Matter
Hospira is recalling 30,880 vials of Vancomycin Hydrochloride for Injection because a hair was found inside a vial and contacted the drug.
Product
Vancomycin Hydrochloride for Injection, USP, 10 grams, Pharmacy Bulk Package - Not For Direct Infusion, For Intravenous Use, packaged in 100 mL glass vial, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-6510-01
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-1847-2017·2017-04-12
Biery Cheese Recalls Marketside Provolone for Listeria Contamination
Biery Cheese, Inc. is recalling Marketside Grab and Go No Smoke Provolone because supplier testing detected Listeria monocytogenes.
Product
Marketside Grab and Go No Smoke Provolone 10.8 oz Set Ups
Category
Food
Distribution
11 states
SevereFDA (Drugs)·D-0641-2017·2017-04-12
SCA Pharmaceuticals Recalls Vancomycin IV Bags Due to Particulate Matter
SCA Pharmaceuticals is recalling 716 bags of Vancomycin HCl IV solution due to the presence of particulate matter.
Product
Vancomycin HCl 1.25 g added to 0.9% Sodium Chloride 250 mL Bag For IV Use Only, Rx Only, SCA Pharmaceuticals, Little Rock, AR 72205, NDC 70004-0923-59
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-1843-2017·2017-04-12
Biery Monterey Jack Cheese with Jalapenos Recalled for Listeria
Biery Cheese is recalling GFS Monterey Jack Cheese with Jalapeno Peppers because supplier tests detected Listeria monocytogenes.
Product
GFS Monterey Jack Cheese with Jalapeno Peppers NET WT. 24 OZ (1.lb 8 OZ) INGREDIENTS: PASTEURIZED MILK, JALAPENO PEPPERS, CHEESE CULTURE, SALT AND ENZYMES. CONTAINS: MILK DISTRIBUTED EXCLUSIVELY BY: GORDON FOOD SERVICE GRAND RAPIDS, MI 49548 UPC 0 93901 77758 4
Category
Food
Distribution
11 states
SevereFDA (Food)·F-1844-2017·2017-04-12
Biery Cheese Recalls Marketside Colby Sharp Cheddar for Listeria
Biery Cheese, Inc. is recalling Marketside Grab and Go Colby Sharp Cheddar cheese because the supplier reported the product tested positive for Listeria monocytogenes.
Product
Marketside Grab and Go Col. Sharp Cheddar 10.8 oz Set Ups
Category
Food
Distribution
11 states
SevereFDA (Food)·F-1842-2017·2017-04-12
Biery Cheese Recalls Finlandia Sriracha and Jalapeno Jack Cheese for Listeria
Biery Cheese, Inc. is recalling Finlandia Sriracha Jack and Jalapeno Jack cheese because the products tested positive for Listeria monocytogenes.
Product
FINLANDIA SRIRACHA JACK & JALAPENO JACK CHEESE NET WT. 12 OZ. (340g) SRIRACHA JACK INGREDIENTS: PASTEURIZED MILK, CULTURES, SALT, JALAPENOS, CAYENNE GARLIC, CITRUS POWDER, ENZYMES CONTAINS: MILK JALAPENO JACK INGREDIENTS: PASTEURIZED MILK, RED AND GREEN JALAPENO PEPPERS…
Category
Food
Distribution
11 states
SevereFDA (Drugs)·D-0645-2017·2017-04-12
SCA Pharmaceuticals Recalls Vancomycin HCl IV Bags Due to Particulate Matter
SCA Pharmaceuticals is recalling 62 bags of Vancomycin HCl 750 mg IV bags due to the presence of particulate matter.
Product
Vancomycin HCl 750 mg added to 5% Dextrose 250 mL For IV Use Only, Rx Only, SCA Pharmaceuticals, Little Rock, AR 72205, NDC 70004-0918-40
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1744-2017·2017-04-12
Recall of Curity Sodium Chloride Dressings Due to Sterility Compromise
Covidien LLC is recalling Curity Sodium Chloride Dressings because the sterile barrier is breached, compromising sterility. The recall affects lots with expiration dates from February 2017 through November 2019.
Product
Covidien Curity Sodium Chloride Dressing , 6 x 6-3/4 (15.2 cm x 17.1 cm), Sterile Item Code: 3339 Curity Sodium Chloride Dressing is indicated for use on exudating and/or infected wounds
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1745-2017·2017-04-12
Recall of Curity Saline Dressings Due to Compromised Sterility
Covidien LLC is recalling Curity Saline Dressings because the sterile barrier was breached, compromising sterility. The recall covers lots with expiration dates from February 2017 through November 2019.
Product
Covidien Curity Saline Dressing 8' x 4 (20.3cm x10.2 cm), Sterile Item Code: 3606 Curity sodium chloride dressing is saturated in a 20% hypertonic saline solution. The dressing is designed to help promote biological cleansing within the wound and aid in the autolytic…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1752-2017·2017-04-12
Philips BrightView X Gamma Camera Recall for Brake Hub Assembly Error
Philips is recalling BrightView X 3/4 gamma cameras because a brake hub assembly error can cause the detector to backdrive.
Product
BrightView X 3/4 model number 882479 BrightView and BrightView X are gamma cameras designed for single or dual detector nuclear imaging accommodating a broad range of Emission Computed Tomography (ECT) studies. The cameras can be used to perform planar static, dynamic, gated…
Category
Medical Device
Distribution
29 states
HighFDA (Food)·F-1877-2017·2017-04-12
IKEA Recalls Choklad Ljus Milk Chocolate for Undeclared Allergens
IKEA is recalling Choklad Ljus Milk Chocolate bars due to undeclared milk, hazelnut, and almond ingredients.
Product
Choklad Ljus Milk Chocolate Net Wt 3.5 OZ; IKEA Produced in Spain For: IKEA Food Services, AB, Almhultsgatan 2, SE-21586 Malmo, Sweden.
Category
Food
Distribution
24 states
HighFDA (Food)·F-1873-2017·2017-04-12
IKEA Recalls Dark Chocolate Bars for Undeclared Milk, Almond, and Hazelnut
IKEA is recalling specific dark chocolate bars because they contain undeclared milk, almond, and hazelnut. Consumers with allergies to these ingredients should not eat the product.
Product
Dark Chocolate bars Choklad Mork Dark Chocolate, Net Wt. 3.5 OZ. AND Chokland Mork Dark Chocolate 70%, Net Wt. 3.5 OZ. Produced in Spain For: IKEA Food Services, AB, Almhultsgatan 2, SE-21586 Malmo, Sweden.
Category
Food
Distribution
24 states
HighFDA (Food)·F-1878-2017·2017-04-12
IKEA Recalls Chocolate Products for Undeclared Milk, Almond, and Hazelnut Allergens
IKEA is recalling specific chocolate products due to undeclared milk, almond, and hazelnut allergens. Consumers with allergies should not consume these items.
Product
Choklad Not; Milk Chocolate with hazelnut Net Wt 3.5 OZ; IKEA Produced in Spain For: IKEA Food Services, AB, Almhultsgatan 2, SE-21586 Malmo, Sweden.
Category
Food
Distribution
24 states
HighFDA (Devices)·Z-1707-2017·2017-04-12
Philips IntelliVue MX4O Monitor Recall for Alarm Failure
Philips is recalling IntelliVue MX4O Patient Wearable Monitors that may fail to switch to Monitor Mode with audible alarms if the connection to the central system is lost.
Product
Philips IntelliVue MX4O WLAN Patient Wearable Monitor Product: 865352 Exchange part (service numbers): 453564615311 TELE PWM,802.lla/b/g,ECG only, US only 453564615331 TELE PWM,802.1 1 a/b/g,ECG&Sp02, US only Product Usage: Indicated for use by health care professionals…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1741-2017·2017-04-12
Recall of Sterile Eye Pads Due to Compromised Sterility Barrier
Covidien is recalling Curity Eye Pads because the sterile barrier was breached, potentially compromising sterility. The recall affects units distributed worldwide.
Product
Covidien Curity Eye Pad Item Code: 91650 The sterile eye pad is a device that consists of a pad made of various materials, such as gauze and cotton, intended for use as a bandage over the eye for protection or absorption of secretions. It is supplied sterile to allow for use…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1876-2017·2017-04-12
IKEA Recalls Chocolate Wafers for Undeclared Hazelnut and Almond
IKEA is recalling Godis Chokladran chocolate wafers because the packaging fails to declare hazelnut and almond ingredients, posing a risk to consumers with allergies.
Product
Godis Chokladran Wafers filled and covered with Milk chocolate; Net Wt 5.9 OZ; IKEA Produced in Spain For: IKEA Food Services, AB, Almhultsgatan 2, SE-21586 Malmo, Sweden.
Category
Food
Distribution
24 states
HighFDA (Devices)·Z-1751-2017·2017-04-12
Philips BrightView XCT Gamma Cameras Recalled for Brake Hub Assembly Error
Philips is recalling 90 BrightView XCT gamma cameras because a brake hub assembly error can cause the detector to backdrive.
Product
BrightView XCT model number 882482 BrightView and BrightView X are gamma cameras designed for single or dual detector nuclear imaging accommodating a broad range of Emission Computed Tomography (ECT) studies. The cameras can be used to perform planar static, dynamic, gated, and…
Category
Medical Device
Distribution
29 states
HighCPSC·17130·2017-04-12
Customatic Recalls Adjustable Beds Due to Electric Shock Hazard
Customatic Beds is recalling about 50,000 adjustable bed bases because side-mounted AC outlets may be incorrectly wired, posing an electric shock hazard.
Product
Adjustable beds
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Food)·F-1874-2017·2017-04-12
IKEA Recalls Chocolate Squares for Undeclared Milk, Almond, and Hazelnut
IKEA is recalling Choklad Lingon & Blabar chocolate squares due to undeclared milk, almond, and hazelnut ingredients.
Product
Choklad Lingon & Blabar Assortment of milk chocolate Squares with lingonberry pieces and dark chocolate squares with bilberry pieces; Net Wt 6.3 OZ; IKEA Produced in Spain For: IKEA Food Services, AB, Almhultsgatan 2, SE-21586 Malmo, Sweden.
Category
Food
Distribution
24 states
HighFDA (Food)·F-1875-2017·2017-04-12
IKEA Recalls Chocolate Products Due to Undeclared Milk, Almond, and Hazelnut
IKEA is recalling specific chocolate products, including Godis Chokladkrokant, due to undeclared milk, almond, and hazelnut ingredients.
Product
Godis Chokladkrokant Milk chocolate with butterscotch pieces; Net Wt 15.9 OZ; IKEA Produced in Spain For: IKEA Food Services, AB, Almhultsgatan 2, SE-21586 Malmo, Sweden.
Category
Food
Distribution
24 states
HighFDA (Devices)·Z-1743-2017·2017-04-12
Sterile Saline Dressing Recalled Due to Compromised Sterility Barrier
FDA is recalling Kerlix Super Sponge Saline Dressings because the sterile barrier is breached, potentially compromising sterility.
Product
Covidien Kerlix Super Sponge Saline Dressing, Sterile Item Code: 3338 Curity sodium chloride dressing is saturated in a 20% hypertonic saline solution. The dressing is designed to help promote biological cleansing within the wound and aid in the autolytic debridement process.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1750-2017·2017-04-12
Philips Recalls 84 BrightView SPECT Gamma Cameras Due to Brake Hub Defect
Philips is recalling 84 BrightView SPECT gamma cameras because a brake hub assembly error can cause the detector to backdrive.
Product
BrightView SPECT model number 882480 BrightView and BrightView X are gamma cameras designed for single or dual detector nuclear imaging accommodating a broad range of Emission Computed Tomography (ECT) studies. The cameras can be used to perform planar static, dynamic, gated…
Category
Medical Device
Distribution
29 states
HighFDA (Devices)·Z-1742-2017·2017-04-12
Recall of Sterile Wound Dressings Due to Compromised Sterility Barrier
Covidien is recalling Curity Wet Dressings because the sterile barrier was breached, potentially compromising sterility. The recall affects units distributed worldwide.
Product
Covidien Curity Wet Dressing 8 x 4 (20.3 cm x 10.2 cm), Sterile Item Code: 3337 Curity sodium chloride dressing is saturated in a 20% hypertonic saline solution. The dressing is designed to help promote biological cleansing within the wound and aid in the autolytic…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1746-2017·2017-04-12
BD Vacutainer Blood Collection Tubes Recalled for Stopper Pullout Risk
Becton Dickinson is recalling specific lots of BD Vacutainer Buffered Sodium Citrate blood collection tubes because stoppers may pull out during use.
Product
BD Vacutainer Buffered Sodium Citrate: (9NC) Blood Collection Tubes, 4.5 mL, 13 x 75 mm, Mfd: Becton Dickinson and Company Product Usage: The BD Vacutainer Safety Coagulation tube is an evacuated blood collection Tube that provides means of collecting, transporting and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1740-2017·2017-04-12
Recall of Sterile Eye Pads Due to Compromised Sterility Barrier
Covidien LLC is recalling Curity Eye Pads because the sterile barrier was breached, potentially compromising sterility.
Product
Covidien Curity Eye Pad Oval, 1-5/8 x 2-5/8 (4.2 cm x 6.7 cm), Sterile Item Code: 2841 The sterile eye pad is a device that consists of a pad made of various materials, such as gauze and cotton, intended for use as a bandage over the eye for protection or absorption of…
Category
Medical Device
Distribution
Distributed nationwide