The Recall Desk

State

Georgia product recalls

73,824 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.

These figures cover only the 9,635 recalls whose distribution notice names Georgia specifically. The 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

51726–51750 of 83459

  • SevereFDA (Devices)·Z-0647-2017·2016-12-14

    Centurion Multi-Med Single Lumen Catheters Recalled for Embolism Risk

    Centurion Medical Products is recalling 1,000 Multi-Med Single Lumen Catheter kits because excess material at the catheter tip may separate and cause an embolism.

    Product
    Multi-Med Single Lumen Catheters sold in Centurion convenience kits. The Multi-Med catheter is indicated for use in patients requiring administration of solutions, blood sampling, and central venous pressure monitoring.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0178-2017·2016-12-14

    North American Rescue Recalls Advance Trauma Kits Due to Sterility Concerns

    North American Rescue LLC is recalling Advance Trauma Kits because the manufacturer has concerns regarding the sterility of the eye wash irrigating solution.

    Product
    Advance Trauma Kit - Product Code 85-0742, 85-0746, 85-0745, 85-0639, 85-0744, 85-0744, 85-0741, North American Rescue
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0702-2017·2016-12-14

    Thayer MANOS EX Surgical Device Recalled for Missing Safety Warning

    Thayer Intellectual Property, Inc. is recalling 339 MANOS EX surgical devices because customers were not notified of a critical safety warning regarding device bending and breakage.

    Product
    MANOS EX (CAT#TY-12-101) Product Usage: Carpal Tunnel Release: as a tool for tissue release of the transverse carpal ligament in patients with Carpal Tunnel Syndrome who fail conservative therapy. Plantar Fasciotomy: as a tool for tissue recession in patients with plantar…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0672-2017·2016-12-14

    Mondelez Recalls Oreo Fudge Creme Cookies for Undeclared Milk Allergen

    Mondelez Global LLC is recalling Oreo Fudge Creme cookies (Original and Mint varieties) because milk is not declared on the ingredient list.

    Product
    Nabisco Oreo Fudge Creme Mint Variety, Net Wt. 11.3 oz Distributed by: Mondelez Global LLC East Hanover, NJ UPC 044000026967
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0668-2017·2016-12-14

    Saputo Recalls Italian White Trim Cheese Due to Foreign Material

    Saputo Cheese USA is recalling 558 lbs of Italian White Trim cheese after a food service customer reported finding white plastic in the product.

    Product
    ITALIAN WHITE TRIM; Pasteurized Milk, Cheese Cultures, Salt, Enzymes. UPC: #063549076820 Saputo code: #107682
    Category
    Food
    Distribution
    24 states
  • SevereFDA (Food)·F-0597-2017·2016-12-14

    OLMA-XXI Recalls Smoked Salmon Due to Listeria Contamination Risk

    OLMA-XXI INC. is recalling 5,530 units of Premium Norwegian Salmon, Smoked, due to potential contamination with Listeria monocytogenes.

    Product
    Premium Norwegian Salmon, Smoked, slice 8oz (227g), UPC # 856687004288, Keep refrigerated
    Category
    Food
    Distribution
    13 states
  • SevereFDA (Devices)·Z-0701-2017·2016-12-14

    3M Recalls Universal Electrosurgical Pads Due to Unintended Material Defect

    3M is recalling Universal Electrosurgical Pads because an unintended process liner may impede the safe return of electrosurgical current, increasing the risk of patient burns.

    Product
    3M Universal Electrosurgical Pad, REF 9130 (100 pads / case) and 3M Universal Electrosurgical Pad with Cord, REF 9135-LP (40 pads / case) Product Usage: 3M Universal Electrosurgical Pads are designed to work with most electrosurgical unite (ESU) for virtually every…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0179-2017·2016-12-14

    North American Rescue Recalls K-9 Trauma Field Kits Due to Sterility Concerns

    North American Rescue LLC is recalling K-9 Trauma Field Kits because the manufacturer has concerns about the sterility of the included eye wash irrigating solution.

    Product
    K-9 Trauma Field Kit - Product Code 80-0211, 80-0304, 80-0209, 80-0210, 80-0300, 80-0301, North American Rescue
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V900000·2016-12-14

    Mercedes-Benz Recalls Vehicles for Potential Axle Bolt Fracture Risk

    Mercedes-Benz is recalling certain 2015-2016 models because axle bolts may not have been assembled correctly, potentially fracturing and causing vehicle instability.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ ML250, AMG GL63, GL550, ML400
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0180-2017·2016-12-14

    North American Rescue Recalls Amphibious Trauma Kits Due to Sterility Concerns

    North American Rescue is recalling Amphibious Trauma Kits because the manufacturer has concerns about the sterility of the eye wash solution.

    Product
    Amphibious Trauma Kit - Product Code 85-0639, North American Rescue
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0598-2017·2016-12-14

    Olma-XXI Recalls Smoked Salmon, Turbot, and Butterfish Due to Listeria Risk

    Olma-XXI Inc. is recalling 2,100 units of smoked sliced salmon, turbot, and butterfish because the products have the potential to be contaminated with Listeria monocytogenes.

    Product
    SALMON, TURBOT, BUTTERFISH, smoked sliced, Net Weight: 8oz (227g), UPC # 856687004448, Keep refrigerated
    Category
    Food
    Distribution
    13 states
  • SevereFDA (Drugs)·D-0175-2017·2016-12-14

    North American Rescue Recalls Range Trauma Kits Due to Sterility Concerns

    North American Rescue LLC is recalling Range Trauma Kit Hardcases because the manufacturer has concerns about the sterility of the eye wash irrigating solution included in the kits.

    Product
    Range Trauma Kit Hardcase - Product Code 85-0889, North American Rescue
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0609-2017·2016-12-14

    Calbee Recalls Black Pepper Green Pea Crisps Due to Undeclared Milk

    Calbee North America is recalling one lot of black pepper flavored green pea crisps because they may contain undeclared milk.

    Product
    HARVEST SNAPS, SNAPEA CRISPS, BLACK PEPPER FLAVORED GREEN PEA CRISPS, NET WT 3.3 OZ (93g)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V899000·2016-12-14

    Mercedes-Benz Recalls Vehicles Due to Electric Power Steering Defect

    Mercedes-Benz is recalling specific 2013-2016 models because a steering control unit defect may cause loss of power steering assist or a fire.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ E350, S550, SL550, S600
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0183-2017·2016-12-14

    North American Rescue Recalls USCG Boat Response Kits Due to Sterility Concerns

    North American Rescue LLC is recalling USCG Boat Response Kits because the manufacturer has concerns about the sterility of the eye wash irrigating solution.

    Product
    USCG Boat Response Kit - Product Code 80-0353, North American Rescue
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0621-2017·2016-12-14

    Eastern Feast Green Raisin Recall for Undeclared Sulfites

    Commerce International Inc. is recalling Eastern Feast Green Raisin products due to undeclared sulfites on the label.

    Product
    Eastern Feast, Green Raisin, 7 oz, 11 oz, and 14 oz plastic containers.
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0671-2017·2016-12-14

    Mondelez Recalls Oreo Fudge Creme Cookies for Undeclared Milk Allergen

    Mondelez is recalling Oreo Fudge Creme cookies because milk is not listed on the ingredient label.

    Product
    Nabisco Oreo Fudge Creme Original Variety, Net Wt. 11.3 oz Distributed by: Mondelez Global LLC East Hanover, NJ UPC 044000026943
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0182-2017·2016-12-14

    North American Rescue Recalls Aid Backpack Kits Due to Sterility Concerns

    North American Rescue LLC is recalling Aid Backpack Kits because the manufacturer has concerns about the sterility of the eye wash irrigating solution.

    Product
    Aid Backpack Kit - Product Code 85-0917, North American Rescue
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V897000·2016-12-14

    Triple E Recalls 2017 Serenity S24CB RVs Due to Wiring Fire Risk

    Triple E is recalling 18 model year 2017 Serenity S24CB recreational vehicles because an incorrectly connected circuit wire poses a fire risk.

    Product
    TRIPLE E — TRIPLE E SERENITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V898000·2016-12-14

    KZRV Recalls 2016-2017 Durango and Venom Trailers for Door Hinge Defect

    KZRV is recalling 2016-2017 Durango and Venom trailers because rear cargo door hinges may have insufficient welds, causing the door to swing down with excessive force.

    Product
    KZRV — KZRV DURANGO, VENOM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0176-2017·2016-12-14

    North American Rescue Recalls Range Trauma Kits Due to Sterility Concerns

    North American Rescue is recalling specific Range Trauma Kits because the manufacturer has concerns about the sterility of the included eye wash solution.

    Product
    Range Trauma Kit ORG - Product Code 80-0213, 80-0299, 80-0298, North American Rescue
    Category
    Medical Device
    Distribution
    Distributed nationwide