State
20,364 recalls have nationwide distribution and so reach Tennessee. 0 additional recalls listed Tennessee specifically in their distribution scope.
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.
Keystone RV Company is recalling 2020–2021 Dutchmen Voltage recreational trailers because the Federal Identification Tag lists incorrect tire pressure (110 PSI instead of 95 PSI), which could cause tire overinflation and increase crash risk.
TJX Companies is recalling about 5,000 Novogratz outdoor metal hanging chairs sold nationwide. These chairs can tip or fall while occupied, or the supporting hooks or chains can break, causing 16 reported injuries including bruises and a mild concussion.
Snow Joe is recalling approximately 26,300 Sun Joe cordless lawn mowers (models 24V-X2-17LM and 24V-X2-17LM-CT) because the mower blade can detach unexpectedly, posing a laceration hazard.
Getinge Servo ventilators may fail to deliver ventilation and stop functioning, potentially causing oxygen deprivation and serious harm to critical care patients.
Tovala is recalling its Gochujang-Glazed Salmon Bowl meal (No. 18-A) because it contains an undeclared peanut allergen. The affected products were distributed nationwide to consumers.
Hamilton's HAMILTON-C6 intensive care ventilator status indicator board may become loose, allowing water or disinfectants to enter the device and cause technical faults that could force the ventilator into unsafe modes where patients breathe unassisted room air.
Tovala is recalling approximately 3,340 Gochujang-Glazed Pork Chop Bowl meals distributed nationwide because they contain undeclared peanuts, which pose an allergy risk to consumers with peanut allergies.
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.
Mckesson is recalling Morrison Medical OB Kits because facility temperature excursions may have reduced product effectiveness. All lots received between June 1 and September 30, 2021 are affected.
Enjoy Life Soft Baked Fruit & Oat Breakfast Ovals (Berry Medley) are being recalled due to potential hard plastic contamination. Approximately 89,736 cases were distributed nationwide in the US and Canada.
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.
McKesson Medical-Surgical Inc. is recalling Beaver-Visitec Ultracell surgical wicks due to facility temperature excursions during storage. Temperature exposure may have impacted product effectiveness, affecting units distributed nationwide between June and September 2021.
Family Dollar recalled multiple oral pain relief products due to storage temperature deviations. The products were distributed to select Family Dollar stores from April 30, 2022 through June 10, 2022.
Enjoy Life Natural Brands is recalling Enjoy Life Brownie Bites Rich Chocolate (UPC 819597013290) due to potential hard plastic pieces in the product. No illnesses have been reported.
B. Braun EVA Gravity Mixing Container 1000 mL units may have been exposed to higher temperatures during storage prior to delivery, potentially affecting product effectiveness. Units distributed nationwide between June and September 2021 are affected.
Family Dollar Stores is recalling Mucinex FastMax Caplets Cold Flu 4CT (SKU 903372) distributed nationwide from April to June 2022 due to improper storage temperature conditions.
Baxter Healthcare is recalling DISCPAC Syringe Tip Caps due to potential packaging failure that could compromise the sterile barrier. The recall affects 602,340 units distributed worldwide.
DeRoyal is recalling specific limb holders and security cuffs due to improperly laced webbing straps that may slide loose, potentially compromising device security.
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.
Enjoy Life Natural Brands is recalling Enjoy Life Soft Baked Cookies Monster (6 oz) due to potential hard plastic pieces. The recall affects 89,736 cases distributed nationwide in the US and Canada with best-by dates between 2/6/2023 and 3/3/2023.
The Vanta Clinician Programmer Application v2.0.2455 may display Error Code 1502, preventing users from programming Vanta implantable neurostimulators. The issue affects 2,920 downloaded software applications distributed worldwide.
3M Grounding Safety Ring pads may have been exposed to excessive temperatures during storage, potentially compromising product effectiveness. The recall affects products distributed nationwide that were received between June and September 2021.
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.
Multiple Alcon contact lens solutions were recalled due to facility temperature excursions during storage and transit that may have reduced product effectiveness. Affected products include Clear Care and Opti Free Replenish solutions distributed nationwide between June and September 2021.
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.