The Recall Desk

State

Tennessee product recalls

20,322 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.

13526–13550 of 20322

  • HighFDA (Devices)·Z-1409-2023·2023-04-26

    Spinal implant screws recalled due to defective titanium material

    Medtronic is recalling 45 units of INFINITY Multi-Axial Screws (lot H5802983) worldwide because incorrect titanium was used, reducing the screw head's gripping strength. No illnesses or injuries have been reported.

    Product
    INFINITY Occipitocervical Upper Thoracic System, MULTI AXIAL SCREW, Size: 4.0mm x 24mm, REF 3604024; for immobilization and stabilization of spinal segment as an adjunct to fusion for the following acute and chronic instabilities of the craniocervical unction, the cervical spine
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1413-2023·2023-04-26

    INFINITY Multi-Axial Spinal Screws Recalled for Titanium Material Defect

    Medtronic is recalling INFINITY Multi-Axial Spinal Screws due to incorrect titanium material used in manufacturing, which reduces the gripping strength of the screw head. The affected screws are used for spinal fusion and stabilization.

    Product
    INFINITY Occipitocervical Upper Thoracic System, MULTI AXIAL SCREW, Size: 4.0mm x 34mm, REF 3604034; for immobilization and stabilization of spinal segment as an adjunct to fusion for the following acute and chronic instabilities of the craniocervical unction, the cervical spine
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1395-2023·2023-04-26

    Instrument Kit Drill Guides Have Incorrect Depth Range

    GEO Instrument Kits for EPS Plates contain drill guides marked with an incorrect depth range (30mm-60mm instead of 10mm-40mm), which could affect surgical implant placement.

    Product
    GEO Instrument Kit for EPS Plate, REF: 70120001, part of the GEO FirstFUSE 1st MTP Joint Arthrodesis Plating System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1412-2023·2023-04-26

    Spinal fixation screws recalled for reduced titanium gripping strength

    Medtronic is recalling 90 INFINITY Multi-Axial Screws (Lot H5806345) due to incorrect titanium material that reduces screw head gripping strength. The defect affects 5 batches distributed in the US and Canada.

    Product
    INFINITY Occipitocervical Upper Thoracic System, MULTI AXIAL SCREW, Size: 4.0mm x 26mm, REF 3604026; for immobilization and stabilization of spinal segment as an adjunct to fusion for the following acute and chronic instabilities of the craniocervical unction, the cervical spine
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1398-2023·2023-04-26

    Pressure Therapy System Recalled for Unauthorized Deep Vein Thrombosis Prevention Claim

    Compass Health Brands is recalling the REX Pressure Therapy System because the user manual incorrectly claims the device can prevent deep vein thrombosis, an indication for which the device was not FDA-cleared.

    Product
    REX (Recovery Exercise X-Trainer) Pressure Therapy System- USER Manual. Intended to temporarily relieve minor muscle aches and/or pains, and to temporarily increase circulation to the treated areas. Models: DVTREX-U and DVTREX -L
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1408-2023·2023-04-26

    Medtronic SenSight Extension Tunneler Kit: manufacturing defect prevents dual-extension passage

    Medtronic recalled approximately 1414 SenSight Extension Tunneler Kits due to a manufacturing defect where dual carriers were machined on only one side, preventing use for passing two extensions simultaneously.

    Product
    Medtronic SenSight Extension Tunneler Kit, REF B31030; The Extension Tunneler Kit is used to assist in the tunneling and passage of extensions for deep brain stimulation
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0537-2023·2023-04-26

    CVS Earwax Removal Drops Recalled for Subpotent Active Ingredient

    CVS-distributed earwax removal drops containing carbamide peroxide are being recalled because the active ingredient may degrade and become subpotent before the labeled expiration date, potentially leaving the product ineffective.

    Product
    Fast Acting Earwax Removal System (carbamide peroxide), 6.5%, 0.5 FL OZ (15 mL) Drops per bottle, OTC, Distributed by: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895, CVS Product # 999532, UPC 0 50428 36475 8.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1406-2023·2023-04-26

    Avanos Ballard Oral Care Swabs recalled for incorrect expiration date labeling

    Avanos Medical is recalling Ballard Oral Care Swabs (codes 12241, 12243, 12251) due to incorrect expiration date labeling. The recall affects 5,475 cases distributed worldwide.

    Product
    Avanos Ballard Oral Care Swab, Bulk Packed, Product Codes: a) 12241, b) 12243, c) 12251
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1391-2023·2023-04-26

    KLS E-Coupling Adapter Recalled for Incorrect Product Identifier Code

    Pro-Dex Inc is recalling 199 KLS E-Coupling Adapter devices due to incorrect Unique Device Identifier (UDI) and GTIN codes. The devices were distributed nationwide.

    Product
    KLS martin Group KLS E-COUPLING ADAPTER REF PDEC-1000-2 E-Coupling Adapter Assembly used to connect the KLS driver (e.g. drill) to a driver bit that fits into the adapter.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1396-2023·2023-04-26

    VITROS COVID-19 Antibody Test Calibrators Recalled for Incorrect Calibrator Levels

    Ortho-Clinical Diagnostics is recalling VITROS Anti-SARS-CoV-2 Total N Antibody Calibrators used in COVID-19 testing due to incorrect calibrator levels in Assay Data Disks, which can delay patient test results.

    Product
    VITROS Immunodiagnostic Products Anti-SARSCoV- 2 Total N Antibody Calibrators programmed onto the Assay Data Disks (ADD) Data Release Versions (DRV): DRVs 6213 through 6218 supporting VITROS Calibrators. Product Code: 6199976
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·23184·2023-04-20

    Lil Anglers Children's Fishing Rods Recalled for Excessive Lead Content

    Lil Anglers is recalling approximately 78,500 children's fishing rods sold as Kid Casters No Tangle Combos because they contain lead levels that exceed the federal lead content ban. Lead ingestion can cause adverse health effects in young children.

    Product
    Children's Fishing Rods sold with Kid Casters No Tangle Combos
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23183·2023-04-20

    DeWALT, Stanley, and Craftsman Fiberglass Sledgehammers Recalled for Detachment Hazard

    Stanley Black & Decker is recalling approximately 2.2 million fiberglass sledgehammers because the head can loosen and detach during use, posing an impact injury hazard. The company has received 192 reports of detachment, including two reported injuries.

    Product
    DeWALT, Stanley and Craftsman Fiberglass Sledgehammers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23746·2023-04-20

    Children's Robes Recalled for Flammability Standards Violation

    Bagno Milano is recalling about 3,600 children's robes sold online from June 2022 through March 2023 because they fail to meet federal flammability standards for children's sleepwear, posing a risk of burn injuries.

    Product
    Children's robes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23186·2023-04-20

    DynaDrive Fresh Water Well Pumps Recalled Due to Electric Shock Risk

    Davey Water Products is recalling about 1,060 DynaDrive Fresh Water Well Pumps because inadequate grounding can pose an electric shock hazard. One electrical shock has been reported in Australia; no incidents have been reported in the United States.

    Product
    DynaDrive Fresh Water Well Pumps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23188·2023-04-20

    NewCosplay Children's Sleepwear Recalled for Flammability Violation

    Taizhou Jiawang Trading Co. is recalling about 868 NewCosplay children's sleepwear garments sold on Amazon from November 2021 through April 2022 because they fail to meet federal flammability standards and pose a burn hazard.

    Product
    Children's sleepwear
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23187·2023-04-20

    NewCosplay Children's Sleepwear Recalled for Flammability Standards Violation

    Changshu Lingshang Trading's NewCosplay children's sleepwear fails to meet federal flammability standards, posing a burn injury risk to children. About 110 units sold on Amazon from October 2021 through May 2022 are affected.

    Product
    Children's sleepwear
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23747·2023-04-20

    Lelinta Multi-Purpose Kids Helmets Recalled for Head Injury Risk

    Lucky Global is recalling about 30 Lelinta Multi-Purpose Kids Helmets sold online at Walmart.com because they do not meet federal safety standards for positional stability and may fail to protect children in a crash.

    Product
    Lelinta Multi-Purpose Kids Helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·23185·2023-04-20

    Rollerblade Fury Inline Skates Recalled Due to Fall Hazard

    Rollerblade USA is recalling about 13,400 Fury Inline Skates because the rear brake support can fracture or separate, reducing stability and increasing the risk of falls. No injuries have been reported to date.

    Product
    Rollerblade® Fury Inline Skates and Rollerblade® Fury brake supports
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0705-2023·2023-04-19

    Frozen Organic Strawberries Recalled Due to Hepatitis A Contamination

    Multiple brands of frozen organic strawberries are being recalled due to potential hepatitis A contamination. The recall affects products distributed across the United States.

    Product
    Simply Nature Organic Strawberries, frozen, net wt. 24 oz., 8 packages per case. UPC 4099100256222. Product of Mexico. Distributed by Aldi Batavia, IL Vital Choice Organic Strawberries, frozen, net wt. 16 oz., 20 packages per case. UPC 834297005024. Product of Mexico. Distribut
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0704-2023·2023-04-19

    Trader Joe's Frozen Tropical Fruit Blend Recalled for Hepatitis A Risk

    Scenic Fruit Company is recalling Trader Joe's Organic Tropical Fruit Blend and related products distributed nationwide and regionally due to potential Hepatitis A contamination from Mexican strawberries. Five lot numbers with Best By dates from April to June 2024 are affected.

    Product
    Trader Joes Organic Tropical Fruit Blend, frozen, net wt. 16 oz., 24 bags per case, SKU 051191. UPC 00511919. This product contains strawberries from Mexico. Distributed by Trader Joe's Monrovia, CA.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0703-2023·2023-04-19

    Frozen Organic Strawberries Recalled for Potential Hepatitis A Contamination

    Frozen Organic Strawberries sold under multiple brands (Kirkland Signature, Trader Joe's, and others) are being recalled due to potential hepatitis A contamination. Do not consume; discard or return to retailer.

    Product
    Frozen Organic Strawberries, Kirkland Signature, frozen, net wt. 4lb., 9 packages per case, Costco Item 904984. UPC 096619140404. Distributed by Costco Warehouse Corporation, Seattle, WA. Product of Mexico.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0730-2023·2023-04-19

    Meal kits with animal crackers recalled for possible metal shavings

    E S Foods is recalling 65550 5 Days Meal Kits nationwide because animal crackers may contain bronze metal shavings. Consumers should not consume the affected products.

    Product
    65550 5 Days Meal Kit
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1387-2023·2023-04-19

    Step Bladeless Trocars recalled for sterilization failure

    Covidien's Step Bladeless Trocars (Model S101010, Lot P2G0069) are being recalled due to a sterilization process failure that may have resulted in unsterile instruments. Use of affected units may lead to infection or vision loss in eye procedures.

    Product
    Step Bladeless Trocars, 10 mm cannula and dilator with radially expandable sleeve and 5 - 10 mm reducer, Product Number S101010
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1352-2023·2023-04-19

    Flex-Neck Catheter Repair Kit design test product inadvertently distributed to patients

    Merit Medical Systems inadvertently distributed 17 Flex-Neck Catheter External Repair Kits intended for design verification testing to customers in Maryland, Michigan, Ohio, and Texas.

    Product
    Flex-Neck Catheter External Repair Kit REF CE-1400 LOT CE-1400/A
    Category
    Medical Device
    Distribution
    Distributed nationwide