The Recall Desk

State

Georgia product recalls

72,966 recalls have nationwide distribution and so reach Georgia. 9,588 additional recalls listed Georgia specifically in their distribution scope.

What the numbers show

Total
9,588
Critical
1,464
Severe
2,164
Most recent
2026-09-09

Of the 9,588 recalls naming Georgia we have scored against our rubric, 1,464 (15%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,164 (23%) are Severe.

These figures cover only the 9,588 recalls whose distribution notice names Georgia specifically. The 72,966 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

4976–5000 of 82554

  • HighFDA (Food)·H-0096-2026·2025-10-29

    Ready rice pouches recalled over possible presence of stones in product

    Mars Foods US is recalling 1,075 cases of Ben's Original Ready Rice Long Grain & Wild because of the possible presence of stones in the product.

    Product
    Ben's Original Ready Rice Long Grain & Wild, 8.8oz., UPC 0 54800 42331 6. 12 retail units per wholesale case
    Category
    Food
    Distribution
    9 states
  • HighFDA (Drugs)·D-0097-2026·2025-10-29

    Opdualag injection vials recalled from one lot over sterility assurance

    Bristol-Myers Squibb is recalling 12,778 vials of Opdualag (nivolumab and relatlimab-rmbw) injection from one lot for lack of assurance of sterility.

    Product
    OPDUALAG — OPDUALAG (NIVOLUMAB AND RELATLIMAB-RMBW)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0231-2026·2025-10-29

    ECG trunk cables recalled because improper module placement can cause overheating

    GE is recalling 29,225 MAC VU360 acquisition trunk cables and module holders because incorrect placement of the module can wear the cable until it overheats in use.

    Product
    MAC VU360 Acquisition Trunk Cable and Module Holder, high performance, multichannel resting electrocardiograph, Model Number 2030360-001, Product Codes VU2 and VU4
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0031-2026·2025-10-29

    Gabapentin blister packs recalled after unknown impurity exceeded specification

    The Harvard Drug Group is recalling Gabapentin Capsules USP 100 mg in 10-capsule blister packs after routine stability testing returned an out-of-specification result for highest unknown impurity.

    Product
    GABAPENTIN — GABAPENTIN (GABAPENTIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0032-2026·2025-10-29

    Cetirizine hundred count bottles recalled over tablets imprinted with wrong identifier

    JB Chemicals is recalling 9,936 hundred-count bottles of Cetirizine Hydrochloride Tablets USP 10 mg because the tablets were imprinted with the wrong identification code.

    Product
    CETIRIZINE HYDROCHLORIDE — CETIRIZINE HYDROCHLORIDE (CETIRIZINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0033-2026·2025-10-29

    Cetirizine tablets recalled because tablets were imprinted with the wrong identifier

    JB Chemicals is recalling 13,440 bottles of Cetirizine Hydrochloride Tablets USP 10 mg because the tablets were imprinted with the wrong identification code.

    Product
    CETIRIZINE HYDROCHLORIDE — CETIRIZINE HYDROCHLORIDE (CETIRIZINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0095-2026·2025-10-29

    Zicam fruit drops recalled because label omitted elderberry as an ingredient

    Church & Dwight is recalling 21,912 bottles of Zicam Medicated Fruit Drops Elderberry Flavor because the label failed to list elderberry as an ingredient.

    Product
    ZICAM COLD REMEDY MEDICATED FRUIT DROPS - ELDERBERRY — ZICAM COLD REMEDY MEDICATED FRUIT DROPS - ELDERBERRY (ZINC ACETATE ANHYDROUS, ZINC GLUCONATE, AND SAMBUCUS NIGRA FLOWERING TOP)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0034-2026·2025-10-29

    Olopatadine eye drops recalled after unspecified impurity exceeded specification limit

    USV Private Limited is recalling 8,952 bottles of Olopatadine Hydrochloride Ophthalmic Solution USP 0.1% after an unspecified impurity exceeded the specification limit.

    Product
    Olopatadine Hydrochloride Ophthalmic Solution USP 0.1 %, 5 mL (0.17 FL OZ) bottles, Manufactured for: SOLA PHARMACEUTICALS LLC, Baton Rouge, LA 70810, NDC 70512-0520-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0228-2026·2025-10-29

    Forty six millimetre locking screws recalled over wrong length on packaging

    Synthes is recalling 120 low profile locking screws because 42mm screws were packaged and labeled as 46mm and 46mm screws were labeled as 42mm, though the etched length is correct.

    Product
    LOW PROF LCKNG SCREW, F/IM NAIL 5.0MM / L, 46MM / XL25/ STER. Product Code: 04.045.346TS. Used in RFN-ADVANCEDTM Retrograde Femoral Nailing (RFNA) System and the Tibial Nail Advanced System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0230-2026·2025-10-29

    Foot plating systems recalled to remove a sterilization option from instructions

    CPM Medical Consultants is updating the Fuse ULTRA Foot Plating System instructions for use to remove a sterilization option that does not apply in the United States.

    Product
    Fuse ULTRA Foot Plating System Instructions for Use. Models: OS200400, OS200401, OS328017, OS200020L, OS200025L, OS200120L, OS200125, OS200125L, OS200135, OS200324, OS200325, OS200326, OS328026, OS328028C, OS216150, OS218150, OS292110, OS292120, OS292160, OS292200, OS200516, O
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0229-2026·2025-10-29

    Locking bone screws recalled after packaging labeled with the wrong length

    Synthes is recalling 122 low profile locking screws because 42mm screws were packaged and labeled as 46mm and 46mm screws were labeled as 42mm, though the etched length is correct.

    Product
    LOW PROF LCKNG SCREW, F/IM NAIL 5.0MM / L, 42MM / XL25/ STER. Product Code: 04.045.342TS. Used in RFN-ADVANCEDTM Retrograde Femoral Nailing (RFNA) System and the Tibial Nail Advanced System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0037-2026·2025-10-29

    Bupropion extended release tablets recalled after failing tablet specifications

    Graviti Pharmaceuticals is recalling 46,512 bottles of Bupropion Hydrochloride Extended-Release Tablets USP (XL) 300 mg from one batch for failed tablet specifications.

    Product
    BUPROPION HYDROCHLORIDE — BUPROPION HYDROCHLORIDE (BUPROPION HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateNHTSA·25V736000·2025-10-28

    Jayco motorhome certification labels may reverse front and rear axle data

    Jayco is recalling certain 2025-2026 Entegra Condor and Jayco Granite Ridge motorhomes because the certification label may have the front and rear axle information reversed.

    Product
    ENTEGRA — ENTEGRA, JAYCO CONDOR, GRANITE RIDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V735000·2025-10-27

    Tesla Cybertruck accessory light bar can loosen from the windshield

    Tesla is recalling certain 2024 Cybertruck vehicles fitted with a service-installed off-road light bar because an incorrect surface primer may allow the light bar to loosen and detach.

    Product
    TESLA — TESLA CYBERTRUCK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·035-2025·2025-10-27

    E.A. Sween Recalls Pulled Pork Sandwiches Due to Plastic Contamination

    E.A. Sween Company is recalling approximately 127,887 pounds of pulled pork sandwiches that may contain pieces of plastic. The products were distributed nationwide.

    Product
    E.A. Sween Company — E.A. Sween Company Recalls Pulled Pork Sandwich Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·034-2025·2025-10-25

    Hormel Foods recalls frozen ready-to-eat chicken for metal contamination

    Hormel Foods is recalling about 4.8 million pounds of frozen ready-to-eat chicken products that may contain metal pieces.

    Product
    Hormel Foods Corporation — Hormel Foods Corporation Recalls Ready-To-Eat Frozen Chicken Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V727000·2025-10-24

    Forest River toy hauler fresh water tank can detach when full

    Forest River is recalling certain 2021 XLR Toy Hauler travel trailers because the mounting brackets may be improperly located or secured, allowing the fresh water tank to detach when full.

    Product
    FOREST RIVER — FOREST RIVER XLR TOYHAULER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V729000·2025-10-24

    Ford moonroof wind deflectors can detach from the vehicle

    Ford is recalling certain 2021-2023 Expedition, Navigator, F-150 and Super Duty vehicles because the moonroof wind deflector clips may be inadequately attached, letting the deflector detach.

    Product
    FORD — FORD, LINCOLN F-150, EXPEDITION, NAVIGATOR, F-250 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V725000·2025-10-24

    Mercedes-Benz Recalls Sprinter 2500 Vehicles Due to Frame Defect

    Daimler Vans USA is recalling 2023-2024 Mercedes-Benz Sprinter 2500 vehicles because a frame member may not be reinforced properly, reducing third-row seat structural integrity.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ SPRINTER 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·033-2025·2025-10-24

    LSI, Inc. Recalls BBQ Pork Jerky Due to Possible Metal Contamination

    LSI, Inc. is recalling BBQ pork jerky because pieces of metal were found in the product. No injuries have been reported, but consumers should not eat the product.

    Product
    LSI, Inc. — LSI, Inc. Recalls BBQ Pork Jerky Product Due To Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·25E070000·2025-10-24

    Ford Recalls 10R80 Automatic Transmissions for Missing Bearing

    Ford is recalling specific 10R80 re-manufactured automatic transmissions used in 2017-2021 Ford and Lincoln vehicles because a missing T10 bearing may prevent the vehicle from holding the Park position.

    Product
    POWER TRAIN:AUTOMATIC TRANSMISSION recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V731000·2025-10-24

    Ford Recalls 2022-2023 F-150 Lightning BEV for Rear Lightbar Defect

    Ford is recalling 2022-2023 F-150 Lightning BEVs previously repaired under recall 23V418 because rear lightbar microcracks can cause inoperative or flickering reverse lights.

    Product
    FORD — FORD F-150 LIGHTNING BEV
    Category
    Vehicle
    Distribution
    Distributed nationwide