The Recall Desk

State

Connecticut product recalls

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

About recalls in Connecticut

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 Connecticut 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.

13576–13600 of 20364

  • 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-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
  • 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
  • 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·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
  • 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·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·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·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
  • 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-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
  • 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
  • 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-1360-2023·2023-04-19

    Inflatable Prosthesis Pump Assembly Recalled for Premature Failure Risk

    Coloplast is recalling 9 Titan Pump Assemblies for inflatable penile prostheses due to decreased wall thickness that may cause premature pump failure during normal use.

    Product
    Titan Pump Assembly, Catalog Number 5177701400; inflatable penile Prosthesis
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1365-2023·2023-04-19

    Inflatable Penile Prosthesis Recalled for Potential Pump Failure Risk

    Coloplast is recalling certain Titan NB Infra Zero Ang 16cm inflatable penile prostheses due to thinner-than-standard pump wall thickness that could lead to premature pump failure.

    Product
    Titan NB Infra Zero Ang 16cm, Catalog Number EN88162400; inflatable penile Prosthesis
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1359-2023·2023-04-19

    Titan Touch Pump Inflatable Prosthesis Recalled for Structural Defect Risk

    Coloplast Manufacturing is recalling Titan Touch Pump inflatable penile prostheses due to manufacturing defect causing decreased wall thickness that could lead to premature device failure.

    Product
    Titan Touch Pump, Catalog Numbers 5177502400; inflatable penile Prosthesis
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1376-2023·2023-04-19

    Digital VIPR Oxygen Delivery Systems Recalled for Gauge Malfunction

    Western/Scott Fetzer is recalling 24,287 Digital VIPR oxygen delivery systems for a gauge malfunction that may display incorrect pressure readings. This could allow oxygen tanks to deplete without warning, potentially leaving users without oxygen flow.

    Product
    Digital VIPR ROC-9839 Roberts Oxygen Ready to Use Digital VIPR (head only) ROC-9840, Roberts Oxygen Ready to Use Digital VIPR System (with E-size cylinder) MNDR-600, Western Oxytote DTE Digital VIPR (head only) MNDS-602, Western Oxytote DTE Digital VIPR System (with D-size
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1361-2023·2023-04-19

    Inflatable Penile Prosthesis Recalled Due to Pump Failure Risk

    Coloplast is recalling the Titan Touch NB Infr Zero 16cm inflatable penile prosthesis due to decreased wall thickness in the pump, which may cause premature failure with repeated use.

    Product
    Titan Touch NB Infr Zero 16cm, Catalog Number EN28162400; inflatable penile Prosthesis
    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
  • HighFDA (Devices)·Z-1353-2023·2023-04-19

    PET/CT Imaging System Recall: Software Issue Prevents Image Reconstruction

    Shanghai United Imaging uMI 550 PET/CT imaging system is recalled due to a software defect that may prevent scatter correction during patient scanning, potentially blocking diagnostic PET image generation.

    Product
    Shanghai United Imaging Healthcare Co., Ltd. Positron Emission Tomography (PET) and Computed Tomography (CT), Model uMI 550 Part Number: 88000657 88000057
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0720-2023·2023-04-19

    Meal Kits Recalled Due to Potential Metal Shavings in Animal Crackers

    E S Foods is recalling meal kits nationwide due to potential bronze metal shavings in animal crackers. The recall affects approximately 1,044,918 units.

    Product
    61520 Cheese Stick with 2 Grains and 1 Cup Fruit MB
    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-1368-2023·2023-04-19

    Inflatable Penile Prosthesis Recalled for Risk of Premature Pump Failure

    Coloplast is recalling Titan Touch inflatable penile prostheses with reduced pump wall thickness, which could cause premature failure during use. The defect affects 8 units distributed across the US and multiple European countries.

    Product
    Titan Touch Infr Zero Ang 22cm, Catalog Number ES28222400; inflatable penile Prosthesis
    Category
    Medical Device
    Distribution
    Distributed nationwide