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.

Which agencies issued them

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.

50926–50950 of 83459

  • ModerateFDA (Devices)·Z-1087-2017·2017-02-01

    Atrium Medical 400 Series Express Drains Recalled for Non-Sterile Packaging

    Atrium Medical is recalling 400 Series Express Drains because the outer packaging is not sterile. The recall affects approximately 1.4 million cases distributed worldwide.

    Product
    Atrium Medical 400 Series Express Drains as follows: 4000-100N Express single collection drain with in-line connector 4000-100P Express PreFilled Chest Drain 4020-100N Express dual chamber drain with in-line connectors ( 2 Patient Tubes) 4050-100N Express Blood Recovery…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0446-2017·2017-02-01

    Sun Pharmaceutical Recalls BuPROPion Hydrochloride Tablets for Dissolution Failures

    Sun Pharmaceutical Industries is recalling 11,618 bottles of buPROPion Hydrochloride Extended-release Tablets due to failed dissolution specifications and stability issues.

    Product
    buPROPion Hydrochloride Extended-release Tablets, USP (SR), 200 mg, 60 count bottles, Rx only, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, Manufactured by: Sun Pharmaceutical Ind. Ltd., Halol-Baroda Highway, Halol-389 350, Gujarat, India NDC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0442-2017·2017-02-01

    Mylan Recalls Temozolomide Capsules Due to Broken Capsules and Loose Powder

    Mylan LLC is recalling Temozolomide Capsules, 140 mg, due to customer complaints of broken or crushed capsules resulting in loose powder in the bottles.

    Product
    Temozolomide Capsules, 140 mg, packaged in a) 5-count bottles (NDC 0378-5263-98), b) 14-count bottles (NDC 0378-5263-14), Rx only, Mylan Pharmaceuticals, Inc., Morgantown, WV 26505 USA.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1084-2017·2017-02-01

    Atrium Medical Oasis Pediatric Drain Recalled for Non-Sterile Packaging

    Atrium Medical is recalling Oasis Pediatric Drains because the outer packaging is not sterile. The recall covers 964,463 US cases and 521,975 international cases.

    Product
    Atrium Medical Oasis Pediatric Drain as follows: 3612-100 Oasis Infant/Pediatric drain with in-line connector, ¿ in. tubing, Sims and Pedi connector in bag on back of drain 3612-400 Oasis Infant/Pediatric drain with no in-line connector, ¿ in. tubing, Sims and Pedi connector…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1088-2017·2017-02-01

    Atrium Medical Express Mini 500 Dry Seal Drain Recall

    Atrium Medical is recalling Express Mini 500 dry seal drains because the outer packaging is not sterile.

    Product
    Atrium Medical 16400 Express Mini 500 dry seal drain Product Usage: To evacuate air and/or fluid from the chest cavity or mediastinum.  To help re-establish lung expansion and restore breathing dynamics.  To facilitate postoperative collection and reinfusion of autologous…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1102-2017·2017-02-01

    PerkinElmer AutoDELFIA System Recalled for Potential Plate Loading Failures

    PerkinElmer is recalling AutoDELFIA systems with V3.0 software due to potential plate loading failures that could affect clinical assay results.

    Product
    DELFIA¿ PC with V3.0 Software, Fluorometer, for clinical use Product Number: 1235-8100 Product Usage: The Wallac 1235 AutoDELFIA automatic immunoassay system is designed to automatically perform assays using the DELFIA technology. DELFIA technology is based on the proven…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0448-2017·2017-02-01

    Roxane Recalls Azelastine Nasal Spray Due to Defective Delivery System

    Roxane Laboratories is recalling 74,108 bottles of Azelastine Hydrochloride Nasal Spray because the delivery system failed droplet size testing.

    Product
    Azelastine Hydrochloride Nasal Solution (Nasal Spray), 0.1% (137 mcg per spray), packaged in 30 mL bottles, Rx only, Distributed by: West-Ward Pharmaceuticals Corp., Eatontown, NJ 07724, NDC 0054-0293-99
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1101-2017·2017-02-01

    PerkinElmer AutoDELFIA System Recalled for Potential Plate Loading Failures

    PerkinElmer is recalling AutoDELFIA systems with Version 3.0 software due to potential plate loading failures that could affect clinical assay results.

    Product
    Program Update Package AutoDELFIA¿ 3.0, Fluorometer, for clinical use Product Number: 1235-8110 Product Usage: The Wallac 1235 AutoDELFIA automatic immunoassay system is designed to automatically perform assays using the DELFIA technology. DELFIA technology is based on the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0438-2017·2017-02-01

    Qualitest Recalls Dexamethasone Elixir Due to Failed Impurity Specifications

    Vintage Pharmaceuticals is recalling 2,568 bottles of Dexamethasone Elixir because the product failed impurity and degradation specifications.

    Product
    DEXAMETHASONE ELIXIR, USP, 0.5 mg/5 mL, 8 fl.oz., Rx only, Manufactured for: QUALITEST PHARMACEUTICALS, HUNTSVILLE, AL, NDC 0603-1147-56
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1075-2017·2017-02-01

    Pentax Rigid Laryngostroboscopes Field Correction for Instructions for Use

    Pentax of America is revising the Instructions for Use for Rigid Laryngostroboscopes Models 9106 and 9108.

    Product
    Rigid Laryngostroboscopes The Rigid Laryngostroboscopes, Models 9106 and 9108 are intended to observe glottic action with the use of a stroboscopic light source. The instrument is inserted per-orally when indications consistent with the need for observation are observed.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0439-2017·2017-02-01

    Actavis Recalls Albuterol Sulfate Inhalation Solution Due to Impurities

    Actavis Inc is recalling specific lots of Albuterol Sulfate Inhalation Solution because the product failed impurity specifications for a known degradant.

    Product
    Albuterol Sulfate Inhalation Solution, USP, 0.021% (0.63 mg / 3 mL), 3mL Vials, Rx only, Mfd. for Watson Laboratories Inc., Corona, CA 92880 USA, Mfd. by Cipla Ltd. Verna, Goa India, NDC 0591-3467-53
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereCPSC·17730·2017-01-31

    Simpli Home Recalls Chests of Drawers Due to Tip-Over Hazard

    Simpli Home is recalling about 240 chests of drawers because they can tip over and injure children if not anchored to the wall.

    Product
    Chest of drawers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·17075·2017-01-31

    Bolton Furniture Recalls 4-Drawer Dressers Due to Tip-Over Hazards

    Bolton Furniture is recalling approximately 1,000 4-drawer dressers because they pose a serious tip-over and entrapment hazard to children if not anchored to the wall.

    Product
    Two Over Two 4-drawer dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·17077·2017-01-31

    Brown Jordan Recalls Swivel Patio Chairs Due to Fall Hazard

    Brown Jordan Services is recalling La-Z-Boy swivel patio chairs sold at Sears.com because the base can break during normal use, posing a fall hazard.

    Product
    Swivel Patio Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V064000·2017-01-31

    Van Hool Motorcoach Recall for Steering Box Defect in Cold Weather

    Van Hool is recalling specific 2010-2017 motorcoaches because the steering wheel may be difficult to turn in low temperatures, increasing crash risk.

    Product
    VAN HOOL — VAN HOOL TX45, CX45, TD925, T2145
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17076·2017-01-31

    Casual Living Recalls Swivel Patio Chairs Due to Fall Hazard

    Casual Living Worldwide is recalling about 2 million swivel patio chairs sold at Home Depot because the base can break, causing falls.

    Product
    Swivel Patio Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·17079·2017-01-31

    Teufelberger Recalls Static Ropes and Throwlines Due to Fall Hazards

    Teufelberger is recalling specific static ropes and throwlines because they are mislabeled as certified to NFPA safety standards, posing fall and injury risks to users.

    Product
    Static ropes and throwlines
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·17074·2017-01-27

    IKEA Recalls MYSINGSÖ Beach Chairs Due to Collapse and Amputation Hazards

    IKEA is recalling MYSINGSÖ beach chairs because they can collapse, posing fall and fingertip amputation hazards. Consumers should stop using them and return them for a refund or replacement.

    Product
    MYSINGSÖ beach chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V057000·2017-01-26

    GM Recalls 2016-2017 Chevrolet Cruze for Seat-Back Welding Defect

    General Motors is recalling 2016-2017 Chevrolet Cruze vehicles because a defective weld in the seat-back recliner mechanism may cause the seat to break in a crash, increasing injury risk.

    Product
    CHEVROLET — CHEVROLET CRUZE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V059000·2017-01-26

    Forest River Recalls 2017-2018 Berkshire and Charleston RVs for Fire Risk

    Forest River is recalling 2017-2018 Berkshire and Charleston RVs because a power steering hose may rub a power stud, causing arcing and fluid leaks that increase fire risk.

    Product
    FOREST RIVER — FOREST RIVER BERKSHIRE, CHARLESTON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V062000·2017-01-26

    BMW Recalls 2016-2017 X1 Vehicles for Passenger Air Bag Defect

    BMW is recalling 2016-2017 X1 vehicles because the instrument panel may prevent the front passenger air bag from deploying properly, increasing injury risk in a crash.

    Product
    BMW — BMW X1 SAV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V056000·2017-01-26

    Jayco Recalls 2017 Eagle Fifth-Wheel Trailers Due to Propane Leak Risk

    Jayco is recalling 2017 Eagle fifth-wheel recreational vehicles with the dry camping option because the LP manifold can crack, causing a propane gas leak and increasing fire risk.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER EAGLE
    Category
    Vehicle
    Distribution
    Distributed nationwide