The Recall Desk

State

Tennessee product recalls

20,364 recalls have nationwide distribution and so reach Tennessee. 0 additional recalls listed Tennessee specifically in their distribution scope.

About recalls in Tennessee

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 Tennessee 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.

15301–15325 of 20364

  • ModerateFDA (Drugs)·D-0012-2023·2022-10-26

    Rifampin Capsules recalled due to excess nitrosamine impurity

    Golden State Medical Supply Inc. is recalling Rifampin Capsules, 150 mg, due to elevated levels of 1-Methyl-4-Nitrosopiperazine (MNP) exceeding the FDA interim specification limit of 5 ppm. Affected lots are distributed nationwide.

    Product
    Rifampin Capsules, USP, 150 mg, 30-count bottle, Rx only, Manufactured by Patheon Pharmaceuticals Inc., OH, Packaged by GSMS, Incorporated, CA, NDC 51407-322-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·23022·2022-10-25

    Pine-Sol Multi-Surface and All-Purpose Cleaners Recalled for Bacterial Contamination

    Clorox is recalling Pine-Sol cleaners contaminated with Pseudomonas aeruginosa, a bacteria that risks serious infection in immunocompromised people or those with external medical devices. No illnesses have been reported to date.

    Product
    Pine-Sol® Scented Multi-Surface Cleaners in Lavender Clean®, Sparkling Wave®, and Lemon Fresh scents, CloroxPro® Pine-Sol® All Purpose Cleaners, in Lavender Clean®, Sparkling Wave®, Lemon Fresh, and Orange Energy® scents, and Clorox® Professional™ Pine-Sol® Lemon Fresh Cleaners.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23019·2022-10-20

    Gel Blaster SURGE 1.0 toy guns recalled due to fire hazard

    Gel Blaster is recalling about 62,700 SURGE Model 1.0 toy guns because the lithium-ion battery pack can overheat and ignite. Thirty reports of smoking or fire have been received with no injuries reported.

    Product
    Gel Blaster SURGE 1.0 toy guns
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23020·2022-10-20

    Birds Choice Acrylic Bird Baths Recalled for Fire Hazard

    Backyard Nature Products is recalling Birds Choice acrylic bird baths because sunlight concentrated through the acrylic can overheat nearby wooden surfaces like siding or decking, creating a fire hazard. Two reports of overheating, smoking, fire, and scorching have been received; no injuries reported.

    Product
    Birds Choice Hanging and Pole-Mounted Acrylic Bird Baths
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23021·2022-10-20

    AQUALUNG Apeks Exotec SCUBA Buoyancy Compensators Recalled for Drowning Hazard

    AQUALUNG is recalling Apeks Exotec SCUBA diving buoyancy compensator devices because the dump valve knob can get stuck when inflated, preventing the device from fully inflating and creating a drowning hazard. Approximately 330 units sold nationwide from August 2021 through June 2022 are affected.

    Product
    Apeks Exotec SCUBA Diving Buoyancy Compensator Devices (BCDs)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23018·2022-10-20

    Mittal International Baby Blankets Recalled for Choking and Strangulation Hazard

    TJX is recalling about 108,000 Mittal International baby blankets sold nationwide from September 2021 through July 2022 because loose threads can detach and pose choking, entrapment, and strangulation hazards to infants.

    Product
    Mittal International Baby Blankets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0067-2023·2022-10-19

    Hobbs Medical Polypectomy Snare with Incorrect Expiration Date Label

    Hobbs Medical is recalling Polypectomy Snares (Catalog 7202) with incorrect expiration dates on labels, which could allow use of expired devices. Units were distributed in the US and several other countries from March 2018 to September 2020.

    Product
    Hobbs Medical Polypectomy Snare Catalog Number: 7202
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0020-2023·2022-10-19

    Hobbs Posi-Stop Injection Needle Recalled for Incorrect Expiration Date Labeling

    Hobbs Medical is recalling Hobbs Posi-Stop Injection Needles with certain lot numbers because device labels display an incorrect expiration date, extending the product's indicated shelf life.

    Product
    Hobbs Posi-Stop Injection Needle Catalog Number: 4702
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0061-2023·2022-10-19

    Freeman Pancreatic Flexi-Stent Recall Due to Incorrect Expiration Dates

    Hobbs Medical recalled Freeman Pancreatic Flexi-Stent devices due to incorrect expiration dates on labels that extend the shelf life, potentially allowing use beyond intended timeframe.

    Product
    Freeman Pancreatic Flexi-Stent Catalog Number: 6566
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0054-2023·2022-10-19

    Freeman Pancreatic Flexi-Stent Kit: Incorrect Expiration Date on Device Labels

    Hobbs Medical recalls Freeman Pancreatic Flexi-Stent Kits with incorrect expiration dates on labels that may extend shelf life beyond the actual expiration date.

    Product
    Freeman Pancreatic Flexi-Stent Kit (containing 6568) Catalog Number: 6529
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0018-2023·2022-10-19

    Hobbs Medical Transbronchial Aspiration Needle Recalled for Incorrect Expiration Date

    Hobbs Medical recalls Transbronchial Aspiration Needle (Catalog 4621) for incorrect expiration dates extending shelf life. Affected devices distributed in the US and internationally from March 2018 to September 2020.

    Product
    Hobbs Transbronchial Aspiration Needle Catalog Number: 4621
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0060-2023·2022-10-19

    Freeman Pancreatic Flexi-Stent Recall Due to Incorrect Expiration Date

    Hobbs Medical is recalling Freeman Pancreatic Flexi-Stent devices due to incorrect expiration dates on product labels. The incorrect dates extend the shelf life, potentially allowing use beyond the actual safe expiration.

    Product
    Freeman Pancreatic Flexi-Stent Catalog Number: 6562
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0042-2023·2022-10-19

    Hobbs Biliary Pigtail Stent Kit Label Bears Incorrect Expiration Date

    Hobbs Medical is recalling Biliary Pigtail Stent Kits due to incorrect expiration dates on device labels that extend shelf life beyond actual product expiration, potentially resulting in use of expired devices.

    Product
    Hobbs Biliary Pigtail Stent Kits (containing 3412) Catalog Number: 6028
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0037-2023·2022-10-19

    Hobbs Biliary Pigtail Stent Kits recalled due to incorrect expiration dates

    Hobbs Medical is recalling certain Biliary Pigtail Stent Kits due to incorrect expiration dates on device labels that extend shelf life beyond actual validity. Affected devices distributed between March 2018 and September 2020 may be used beyond their true expiration date.

    Product
    Hobbs Biliary Pigtail Stent Kits (containing 3412) Catalog Number: 6001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0049-2023·2022-10-19

    Freeman Pancreatic Flexi-Stent Kits recalled for incorrect expiration dates

    Hobbs Medical recalls Freeman Pancreatic Flexi-Stent Kits due to mislabeled expiration dates that may extend shelf life. Affected devices with lot numbers ending in R were distributed in the US and internationally from 2018-2020.

    Product
    Freeman Pancreatic Flexi-Stent Kits: Single Pigtail Catalog Number: 6501
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0012-2023·2022-10-19

    Hobbs Medical Flex-Ez Guide Wire With Incorrect Expiration Date

    Hobbs Medical Flex-Ez Guide Wire devices were labeled with an incorrect expiration date that extends shelf life beyond the intended duration. Affected devices were distributed in the US and internationally from March 2018 to September 2020.

    Product
    Hobbs Medical Flex-Ez Guide Wire Disposable For endoscopy procedures Ref: 3412
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0023-2023·2022-10-19

    Hobbs Posi-Stop Injection Needle recalled for incorrect expiration date on label

    Hobbs Medical is recalling Posi-Stop Injection Needles (lot numbers ending in R) due to incorrect expiration dates on labels that extend shelf life. Affected devices were distributed in the US from March 2018 to September 2020.

    Product
    Hobbs Posi-Stop Injection Needle Catalog Number: 4718
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0015-2023·2022-10-19

    Hobbs Medical Polypectomy Snare recalled for incorrect expiration date on label

    Hobbs Medical is recalling its Polypectomy Snare for an incorrect expiration date on the label that extends shelf life. Affected devices were distributed in the US and other countries from March 2018 to September 2020.

    Product
    Hobbs Medical Polypectomy Snare Catalog Number: 4563
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0033-2023·2022-10-19

    Eden Organic Apple Juice Recalled for Excessive Patulin

    Eden Foods is recalling Eden Organic Apple Juice in multiple sizes because excessive levels of patulin, a mycotoxin from rotted apples, were found in certain lots. Rotted apples were not removed during processing.

    Product
    Eden Organic Apple Juice in 32floz., 64floz., and 1.82L sizes, all sizes in glass bottle. Glass bottles packed 12, 32floz. bottles per wholesale case and 6, 64floz. / 1.82L bottles per wholesale case. 32floz. UPC code: 0 0024182 00067 2 32floz. GTIN case code: 1 0024182 00067 9
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0031-2023·2022-10-19

    Hobbs Helical Retrieval Basket recalled for incorrect expiration date

    Hobbs Medical recalled 10 units of its Helical Retrieval Basket due to mislabeled expiration dates that extend the product's shelf life, affecting devices distributed in the US and select countries between 2018 and 2020.

    Product
    Hobbs Helical Retrieval Basket Catalog Number: 4824
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0065-2023·2022-10-19

    Freeman Pancreatic Flexi-Stent label displays incorrect expiration date

    Hobbs Medical is recalling Freeman Pancreatic Flexi-Stent devices with incorrect expiration dates on their labels. The labeling error extends the shelf life beyond the intended timeframe.

    Product
    Freeman Pancreatic Flexi-Stent Catalog Number: 6584
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0064-2023·2022-10-19

    Freeman Pancreatic Flexi-Stent recalled for incorrect expiration date

    Hobbs Medical is recalling Freeman Pancreatic Flexi-Stent devices with incorrect expiration dates on labels that extend perceived shelf life beyond actual device longevity.

    Product
    Freeman Pancreatic Flexi-Stent Catalog Number: 6582
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0035-2023·2022-10-19

    Hobbs Medical Grasping Forceps Recalled for Incorrect Expiration Dates

    Hobbs Medical Grasping Forceps (Catalog 5008) were distributed with incorrect expiration dates that extend shelf life beyond the device's actual safe use period. Affected units with lot numbers ending in 'R' were distributed from March 2018 to September 2020.

    Product
    Hobbs Medical Grasping Forceps Catalog Number: 5008
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0066-2023·2022-10-19

    Freeman Pancreatic Stent Recall: Incorrect Expiration Date on Device Labels

    Freeman Pancreatic Flexi-Stents with incorrect expiration dates on labels may be used beyond their validated shelf life. The recall affects devices distributed in the US and five other countries from March 2018 through September 2020.

    Product
    Freeman Pancreatic Flexi-Stent (contained in kit 6501) Catalog Number: 6541
    Category
    Medical Device
    Distribution
    Distributed nationwide