The Recall Desk

State

Georgia product recalls

20,371 recalls have nationwide distribution and so reach Georgia. 0 additional recalls listed Georgia specifically in their distribution scope.

About recalls in Georgia

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Georgia consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

15851–15875 of 20371

  • HighFDA (Drugs)·D-1401-2022·2022-08-31

    Jet Alert Tablets Recalled for Improper Storage Temperature Conditions

    Jet Alert stimulant tablets distributed nationwide from April to June 2022 are being recalled due to improper storage temperature conditions that may affect product safety and efficacy.

    Product
    JET ALERT TABLET 30 CT distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1372-2022·2022-08-31

    Tylenol and Acetaminophen Products Recalled Due to Improper Storage

    Family Dollar Stores is recalling multiple Tylenol and acetaminophen products due to CGMP deviations involving improper storage temperature conditions. Products were distributed nationwide through specific Family Dollar locations from April 30, 2022 through June 10, 2022.

    Product
    Ready in case ACETAMINOPHEN PM CAPLETS 24 CT SKU 900559; TYLENOL CHILD GRAPE 4 FL OZ SKU 901600 TYLENOL CHILD ORAL SUSPENSION CHERRY 4 FO 913104 TYLENOL INFANTS DROPS DF CHERRY 1OZ SKU 999108 TYLENOL PM CAPLET 24 CT SKU 900603 TYLENOL EXTRA STRENGTH CAPLET 24 CT SKU 91698
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1400-2022·2022-08-31

    ZzzQuil Night Pain Berry Recalled Due to Improper Storage

    ZzzQuil Night Pain Berry 12 FL OZ distributed to Family Dollar Stores from April 30 through June 10, 2022, was held outside appropriate storage temperature conditions, which may compromise medication stability and integrity.

    Product
    ZZZQUIL NIGHT PAIN BERRY 12 FL OZ distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1593-2022·2022-08-31

    Mckesson Ultracell Eye Pledgets Recalled Over Temperature Exposure During Storage

    Mckesson Medical-Surgical is recalling Ultracell Eye Pledgets (Model 40825) due to temperature excursions during storage and transportation between June and August 2021 that may have compromised product effectiveness. Affected units were distributed nationwide from June through September 2021.

    Product
    Ultracell Eye Pledget Ultracell 2 X 6 X 1 mm, Sterile Model Number: 40825
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1564-2022·2022-08-31

    Enjoy Life Soft Baked Cookies Recalled for Hard Plastic Contamination

    Enjoy Life Natural Brands is recalling Soft Baked Cookies Double Chocolate Brownie due to potential hard plastic contamination. Consumers should not eat the affected product.

    Product
    Enjoy Life Soft Baked Cookies Double Chocolate Brownie, 6 oz (170g) UPC 853522000214
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1570-2022·2022-08-31

    FDA Recalls Exacta-Mix 2400 Compounding System for Potential Valve Leaks

    Baxter Healthcare is recalling the Exacta-Mix 2400 compounding system due to potential leaking valves on ports 1-4 in certain lots. Affected units have lot numbers 60316024 and higher.

    Product
    The Exacta-Mix 2400 compounding system, manufactured by Baxter Healthcare Corporation, is a compounding device used in the pharmacy to compound multiple source ingredients into one final solution. This device is not intended for direct patient hook-up.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1579-2022·2022-08-31

    Baxter Syringe Tip Caps Recalled for Potential Sterile Barrier Failure

    Baxter Healthcare Corporation is recalling 168,390 units of DISCPAC Syringe Tip Caps because the packaging may not maintain a sterile barrier, creating a contamination risk.

    Product
    Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Green: a) 25 pack, REF H93869025, b) 100 pack, REF H938674100, c) 100 pack, REF H93869100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1586-2022·2022-08-31

    ABX PENTRA Creatinine Reagent Recalled Due to Temperature Excursion Exposure

    Mckesson Medical-Surgical is recalling ABX PENTRA Creatinine reagent due to facility temperature excursions (June-August 2021) that may have impacted product effectiveness. Affected lots were received nationwide between June 1 and September 30, 2021.

    Product
    a. ABX PENTRA CREATININE 120CP JAFFE 120/130. Ref: A11A01933. b. Reagent General Chemistry Creatinine Model Number: 1220001933
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1595-2022·2022-08-31

    Cadwell Disposable Ground Electrodes Recalled Due to Temperature Exposure

    Cadwell Disposable Ground Electrodes may have reduced effectiveness due to facility temperature excursions between June and August 2021. All units distributed nationwide received between June 1 and September 30, 2021 are affected.

    Product
    Cadwell Disposable Ground Electrodes Grounding Pad 1.25 X 1.75 Inch Dimensions, Disposable Model Number: 302288-000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1402-2022·2022-08-31

    Petroleum Jelly Products Recalled for Improper Storage Conditions

    Family Dollar Stores is recalling three petroleum jelly products (Swan, Baby Love, and Vaseline brands) distributed between April and June 2022 due to storage temperature deviations.

    Product
    SWAN PETROLEUM JELLY 7.5 OZ SKU 910721 BABY LOVE PETROLEUM JELLY 13 OZ SKU 910726 VASELINE PETROLEUM JELLY ORIGINAL 7.5 OZ 2099273 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1568-2022·2022-08-31

    Servo-air Ventilator Systems Lack Required Stability Warning Markings

    Getinge is recalling Servo-air Ventilator Systems because they lack required warning markings about stability risks when stationary. A total of 102 units were distributed in the US; 13,750 units were distributed internationally.

    Product
    Servo-air Ventilator System-The Servo-air Ventilator System is: Intended for respiratory support, monitoring and treatment of pediatric and adult patients. Model Number: 6882000 (equipped with 6881999 mobile cart)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1384-2022·2022-08-31

    Family Dollar Hydrocortisone and Cortizone Creams Recalled for Storage Deviation

    Family Dollar Stores is recalling hydrocortisone cream (1 oz, SKU 910321) and Cortizone 10 Creme (0.5 oz, SKU 910167) distributed April 30 through June 10, 2022, due to improper storage temperature conditions.

    Product
    FS HYDROCORTISONE CREAM 1 OZ SKU 910321 CORTIZONE 10 CREME 0.5 OZ SKU 910167 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1585-2022·2022-08-31

    Medical Device Etching Solution Recalled for Potential Temperature-Related Effectiveness Loss

    ABX Pentra Etching CP solution is recalled due to temperature excursions from June-August 2021 that may have affected product effectiveness. Affected lots were distributed June 1 - September 30, 2021.

    Product
    HORIBA ABX MEDICAL INC ABX PENTRA ETCHING CP System Fluid ABX Pentra Eching Solution CP For ABX Pentra 400 Clinical Chemistry Analyzer 25 mL. Ref: 1220001769
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1568-2022·2022-08-31

    Enjoy Life Chewy Bars Recalled for Hard Plastic Contamination

    Enjoy Life Natural Brands is recalling Chewy Bars - Caramel Blondie due to potential hard plastic pieces. About 89,736 cases were distributed in the US and Canada.

    Product
    Enjoy Life Chewy Bars Caramel Blondie (Chocolate Chip and Caramel), 5.75 oz (165g) UPC 819597011258 and 819597011333
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1420-2022·2022-08-31

    PREVACID Lansoprazole 15mg Capsules Recalled Due to Storage Conditions

    Family Dollar Stores is recalling PREVACID 24HR Lansoprazole 15mg capsules distributed nationwide from April 30 to June 10, 2022, because the product was stored at improper temperatures in violation of manufacturing standards. Consumers should not use this product and should contact Family Dollar Stores for a refund.

    Product
    PREVACID 24HR LANSOPRAZOLE 15MG CAP 14CT distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1606-2022·2022-08-31

    Alere Fertility Test Pregnancy Test Kits Recalled Due to Temperature Damage

    Alere Fertility Test pregnancy test kits distributed in the US have been recalled because temperature excursions during storage may have reduced product effectiveness. All lots received between June 1 and September 30, 2021 are affected.

    Product
    a. ABBOTT RAPID DX N AMERICA LLC Alere Rapid Test Kit Alere Fertility Test hCG Pregnancy Test Urine Sample 30 Tests, Model Number: 92210. b. ABBOTT RAPID DX N AMERICA LLC Alere Rapid Test Kit Alere hCG Dipstick Fertility Test hCG Pregnancy Test Urine Sample 50 Tests Model Num
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1628-2022·2022-08-31

    Medical Lubricating Jelly Recalled Due to Temperature Excursions During Storage

    Mckesson Medical-Surgical is recalling Fisher Scientific Aseptic Control Lubricating Jelly due to temperature excursions from June–August 2021 that may have reduced product effectiveness.

    Product
    FISHER SCIENTIFIC Aseptic Control¿ LUBRICATING JELLY PAP TEST 4OZ(12/PK) Catalog #22998006
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1621-2022·2022-08-31

    Medical Sponges Recalled for Temperature Exposure During Storage

    Mckesson Medical-Surgical is recalling MetriSponge cleaning sponges due to facility temperature excursions that may have compromised product effectiveness during storage and delivery between June and August 2021.

    Product
    METREX RESEARCH CORP SPONGE, METRISPONGE W/METRIZYME (25/BX 4BX/CS) Model Number: 10-4025
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1398-2022·2022-08-31

    AZO YEAST PLUS 20 CT Recalled Due to Improper Storage Conditions

    AZO YEAST PLUS 20 CT has been recalled by Family Dollar Stores due to improper storage temperature conditions that violate CGMP requirements. The product was distributed nationwide from April through June 2022.

    Product
    AZO YEAST PLUS 20 CT distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1565-2022·2022-08-31

    Dental Implant Recall: Nobel Biocare Device Burr Aspiration Risk

    Nobel Biocare is recalling 347 N1 TiUltra TCC dental implants due to a burr that may pose an aspiration risk during surgical implantation. No injuries have been reported.

    Product
    Nobel Biocare N1 TiUltra TCC NP 3.5x13mm
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1581-2022·2022-08-31

    Baxter DISCPAC Syringe Tip Caps Recalled for Potential Sterile Barrier Failure

    Baxter is recalling DISCPAC Syringe Tip Caps due to potential packaging defect that may not maintain sterile barrier. The recall affects 8,500 units distributed worldwide.

    Product
    Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Purple, 100 pack, REF H938677100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1615-2022·2022-08-31

    MedSource IV Start Kit Recalled for Temperature-Related Effectiveness Loss

    McKesson is recalling MedSource IV Start kits due to facility temperature excursions that may have compromised product effectiveness. Affected units were received between June and September 2021.

    Product
    MedSource IV Start kit, 8inch Extension Set IV START KIT, W/SITE LOC/8" EX100/CS Model Number: MS-80047
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1570-2022·2022-08-31

    Enjoy Life Oat Breakfast Ovals Recalled for Hard Plastic Contamination

    Enjoy Life Natural Brands is recalling Enjoy Life Soft Baked Fruit & Oat Breakfast Ovals due to potential hard plastic pieces in the product. Consumers should not consume affected items.

    Product
    Enjoy Life Soft Baked Fruit & Oat Breakfast Ovals Chocolate Chip Banana, 8.8 oz (250g) UPC 819597012576 and 819597012705
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1444-2022·2022-08-31

    AFRIN No Drip Severe Congestion Recalled for Improper Storage Temperature

    Family Dollar Stores is recalling AFRIN No Drip Severe Congestion 0.5 FL oz due to improper storage temperature conditions (CGMP deviation). The product was distributed to specific Family Dollar locations from April 30 through June 10, 2022.

    Product
    AFRIN NO DRIP SEVERE CONGESTION 0.5FL OZ distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1584-2022·2022-08-31

    Surgical Hemostatic Matrix Recalled Due to Temperature Exposure During Storage

    Mckesson is recalling Ethicon SURGIFLO Hemostatic Matrix Kit due to temperature excursions during storage that may have reduced product effectiveness. Affected units were distributed nationwide between June and September 2021.

    Product
    Ethicon SURGIFLO Hemostatic Matrix Kit with Thrombin (6/CS) Ref: 2994 Mfg: FERROSAN MEDICAL DEVICES A/S Indicated in surgical procedures (other than ophthalmic) as an adjunct to hemostasis when control of bleeding by ligature or other conventional methods is ineffective
    Category
    Medical Device
    Distribution
    Distributed nationwide