The Recall Desk

State

Georgia product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

58026–58050 of 83468

  • ModerateFDA (Drugs)·D-0393-2016·2015-12-09

    Geritrex Recalls Unapproved Polyethylene Glycol 3350 Powder Jars

    Geritrex Corporation is recalling Polyethylene Glycol 3350-GRX Powder 100% jars because the FDA determined they are unapproved new drugs and misbranded.

    Product
    Polyethylene Glycol 3350-GRX Powder 100% jars a) 8.4 oz (250 g) (NDC 54162-335-02), b) Net wt. 16.9 oz (500 g) (NDC 54162-335-05), Distributed by: Geritrex Corporation, Mount Vernon, NY 10550
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0362-2016·2015-12-09

    Stryker Duracon Tibial Wedge Implants Recalled for Packaging Integrity Issues

    Stryker is recalling 2,577 Duracon Tibial Wedge implants because they punctured the packaging's Tyvek lids, potentially compromising sterility.

    Product
    Stryker Orthopaedics Duracon Flat Tibial Wedge Cemented use only Sterile. Tibial Wedge is a component of Total Stabilizer Knee which consists of femoral component, tibial insert, modular offset adaptor, femoral/tibial stem extenders and tibial wedges. Tibial wedges are intended…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0366-2016·2015-12-09

    Merz Recalls Radiesse Injectable Implant Due to Incorrect Expiration Date

    Merz North America is recalling 1,616 units of Radiesse (+) Lidocaine Injectable Implant because the expiration date on the packaging is incorrect.

    Product
    Radiesse (+) Lidocaine Injectable Implant 1.5cc, P/N: 8063M0K1. Indicated for subdermal implantation for the correction of moderate to severe facial wrinkles and folds.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0367-2016·2015-12-09

    Merz Recalls Prolaryn Injectable Implant Due to Incorrect Expiration Date

    Merz North America is recalling Prolaryn Injectable Implant 1.0 cc Gel because the expiration date on the label is incorrect.

    Product
    PROLARYN Injectable Implant 1.0 cc Gel, Model No. 8602M0K5. A restorable implant material to aid in surgical reconstructions as a space occupying material in laryngeal surgical procedures for vocal fold medialization and augmentation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0390-2016·2015-12-09

    Geritrex Recalls Unapproved Carbo-O-Philic 40 Cream Tubes Nationwide

    Geritrex Corporation is recalling Carbo-O-Philic 40 Cream tubes because the FDA determined the product is an unapproved new drug and misbranded.

    Product
    Carbo-O-Philic 40 Cream 40% (Urea) tubes, a) 3 oz (85 g) (NDC 54162-640-03) , b) 7 oz (200 g) (NDC 54162-640-07), Rx Only For topical use only, Distributed by Geritrex Corporation, East Mount Vernon, NY 10550
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0389-2016·2015-12-09

    Nephron Recalls Asthmanefrin Racepinephrine Inhalation Solution Due to Discoloration

    Nephron Pharmaceuticals is recalling 32,490 cartons of Asthmanefrin Racepinephrine Inhalation Solution due to discoloration. The FDA classifies this as a Class II recall.

    Product
    Asthmanefrin Racepinephrine Inhalation Solution Bronchodilator Refills (Racepinephrine USP 11.25 mg), 30 individual foil wrapped vials per carton, Manufactured By: nephron pharmaceuticals corporation, Orlando, FL --- NDC 0487-2784-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0343-2016·2015-12-09

    Ormco Recalls Copper NiTi Preformed Archwires Due to Incorrect Labeling

    Ormco is recalling Copper NiTi Preformed Archwires because the transformation temperature listed on the label is incorrect.

    Product
    Copper NiTi Preformed Archwires; Copper NiTi 40 BAF .016X.022 LO Pk10, Part No. 211-0952. Intended to provide tooth movement.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0368-2016·2015-12-09

    Merz Recalls Prolaryn Plus Injectable Implant Due to Incorrect Expiration Date

    Merz North America is recalling Prolaryn Plus Injectable Implants because the expiration date on the labels is incorrect. The recall covers 9,439 units distributed in the US and South Africa.

    Product
    PROLARYN PLUS Injectable Implant 1.0 cc Plus Calcium Hydroxlyapatite (CaHA) Injectable Implant, Model No. 8044M0K5. An injectable implant used to treat vocal fold insufficiency.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0391-2016·2015-12-09

    Geritrex Recalls Unapproved Carbo-O-Philic 40 Gel Topical Urea Product

    Geritrex Corp is recalling Carbo-O-Philic 40 Gel because the FDA determined it is an unapproved new drug and misbranded.

    Product
    Carbo-O-Philic 40 Gel 40% (Urea) NET WT tube, .5 oz (15 g), Rx Only For topical use only, Distributed byGeritrex Corporation 144, Mount Vernon, NY 10550, NDC 54162-016-15
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0388-2016·2015-12-09

    Nephron Recalls Asthmanefrin Inhalation Solution Due to Discoloration

    Nephron Pharmaceuticals is voluntarily recalling Asthmanefrin inhalation solution starter kits due to discoloration. The recall covers 47,754 cartons distributed nationwide.

    Product
    Asthmanefrin Racepinephrine Inhalation Solution Bronchodilator, Starter Kit (Racepinephrine 11.25 mg) 10 individual foil wrapped vials with 1 EZ Breathe Atomizer per carton, Manufactured By: nephron pharmaceuticals corporation, Orlando, FL --- NDC 0487-2784-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0485-2016·2015-12-09

    Northwind Pharmaceuticals Recalls Prednisone Tablets Due to Incorrect NDC Labeling

    Northwind Pharmaceuticals is recalling 40 bottles of Prednisone 20 mg tablets because the NDC number on the container is incorrect.

    Product
    Prednisone 20 mg, Tablet, 10-count bottle, Rx only, Mfg by: HIKMA Pharmaceuticals PO BOX 182400 Amman 11118 Jordan. Dist By: West-Ward Pharmaceuticals Corp., Eatentown, NJ 07724 USA, Repackaged By: Northwind Pharmaceuticals, Indianapolis, IN 46256. NDC 51655-320-53
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereCPSC·16710·2015-12-08

    Kubota Recalls Utility Vehicles Due to Fire Hazard

    Kubota is recalling approximately 11,500 RTV-X1100C utility vehicles because combustible debris can contact the exhaust manifold and ignite, posing a fire hazard.

    Product
    Utility Vehicles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V823000·2015-12-08

    Audi Recalls A6 and A7 Vehicles Due to Passenger Air Bag Defect

    Volkswagen Group of America is recalling 2012-2013 Audi A6 and A7 vehicles because the passenger air bag system may fail to deploy in a crash.

    Product
    AUDI — AUDI A7, A6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16054·2015-12-08

    TCP and Great Value LED Lamps Recalled for Electrical Shock Hazard

    Technical Consumer Products is recalling specific 14-watt LED PAR38 lamps sold at Walmart and electrical distributors due to a risk of electric shock in wet locations.

    Product
    Technical Consumer Products (TCP) and Great Value LED lamps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15V824000·2015-12-08

    Audi Recalls 2015 A3 Cabriolet for Seat Cover Stitching Defect

    Volkswagen is recalling 904 2015 Audi A3 Cabriolets because incorrectly stitched seat covers may prevent side air bags from deploying properly in a crash.

    Product
    AUDI — AUDI A3 CABRIOLET
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V820000·2015-12-07

    Polaris Recalls 2015 GEM Electric Vehicles for Seat Belt Defect

    Polaris is recalling 2015 GEM electric vehicles because seat belt retractors may fail, preventing proper occupant restraint in a crash.

    Product
    GEM — GEM E6S, E4, ELXD, EL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V816000·2015-12-07

    Freightliner Cascadia CNG Vehicles Recalled for Exhaust Fire Risk

    Daimler Trucks North America is recalling 2013-2015 Freightliner Cascadia CNG vehicles because hot exhaust near the pressure relief device may cause gas release and fire.

    Product
    FREIGHTLINER — FREIGHTLINER CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V821000·2015-12-07

    Honda Recalls VFR1200F Motorcycles for Driveshaft Universal Joint Wear

    Honda is recalling 2010, 2012, and 2013 VFR1200F motorcycles because driveshaft universal joint bearings may wear prematurely, potentially causing the joint to separate or break.

    Product
    HONDA — HONDA VFR1200F
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V819000·2015-12-07

    Tiny Idahomes Recalls RVs With Overheating Water Heater Valves

    Tiny Idahomes is recalling 2014-2016 RVs equipped with specific Atwood water heaters that may overheat water, posing a scalding risk.

    Product
    TINY IDAHOMES — TINY IDAHOMES CASCADE, CLEAR CREEK, CARPATHIAN
    Category
    Vehicle
    Distribution
    Distributed nationwide