State
20,324 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.
BioFire Diagnostics is recalling FilmArray GI Panel diagnostic kits due to temperature excursions during shipping that may reduce test performance.
Two Rivers Coffee hot cocoa pods in variety packs may contain undeclared peanut residue. Consumers with peanut allergies should not consume these products and should check the affected product codes.
Mockingbird LLC is recalling about 25,390 Single Strollers because the lower side of the frame can crack, posing a fall risk to children. The company is offering a free frame reinforcement kit.
Polaris is recalling model years 2021–2023 Sportsman 450 and 570 ATVs because an improperly assembled wiring harness can contact the brake line and vehicle frame, resulting in front brake loss and fire.
IKEA is recalling LETTAN flat mirrors because plastic wall fittings can break and cause the mirror to fall, creating a laceration risk. About 22,400 units in the U.S. are affected.
Pfizer is recalling Nurtec® ODT (rimegepant) 75mg tablets because the blister card packaging is not child-resistant as required by law, posing a poisoning risk to children who may access and swallow the contents.
Sunbeam Queen Size Heated Blankets (model 32810027) can overheat, posing fire and burn hazards. The firm has received 13 reports of overheating with no injuries reported. Consumers should stop using them immediately and contact Star Elite for a refund.
STIHL is recalling about 2,700 iMOW docking stations that can short-circuit when exposed to moisture, creating a fire hazard. Eight reports of thermal overheating and two fires have been reported; no injuries.
Ecoxall is recalling sodium hydroxide and potassium hydroxide products sold on Amazon because the packaging does not meet child-resistant requirements under the Poison Prevention Packaging Act. The products pose a risk of chemical burns and skin or eye irritation.
Fredericksburg Farms is recalling about 6,500 scented candles with glass lids because some lids are too tight, causing jars to break when forcibly opened. The company has received four reports of hand lacerations.
The Cardiosave Rescue intra-aortic balloon pump may suddenly stop working due to communication failure between internal circuit boards, interrupting patient therapy and threatening hemodynamic stability.
Snowy Range Blue hand sanitizer is recalled due to FDA findings of methanol, acetaldehyde, and acetal above permissible limits. The product was distributed nationwide across all lot codes.
Datascope Corp. is recalling Cardiosave Hybrid IABP devices due to a connection failure that may cause unexpected shutdown during use. The failure prevents communication between the device's display head and base unit.
Chukar Cherry Company is recalling Cherry Bombs Bits 'n Pieces chocolate candy nationwide due to undeclared hazelnuts, a food allergen.
Datascope Corp. is recalling Cardiosave Rescue Intra-Aortic Balloon Pumps due to a coiled cord cable connection failure that may cause unexpected device shutdown and loss of communication.
Pharmedica USA recalled Purely Soothing 15% MSM Drops nationwide due to non-sterility concerns. The voluntary Class I recall affects approximately 1,904 bottles distributed via e-commerce and trade shows.
The Cardiosave Hybrid intra-aortic balloon pump (IABP) is being recalled because it may unexpectedly shut down due to communication loss between internal components. The shutdown could interrupt therapy in cardiac patients and compromise their hemodynamic stability.
Denver Solutions recalls 8,136 units of Phenylephrine HCl IV solution nationwide due to manufacturing practice deviations. The FDA classified this Class II recall as affecting prescription injectable solutions distributed to hospitals and government facilities.
Nutraceutical Corporation is recalling NatraBio Cold & Sinus Nasal Spray (0.8 FL Oz) lot 222016 due to manufacturing deviations and product discoloration. The product was distributed nationwide.
St. Jude Medical is recalling 317 CardioMEMS PA Sensors due to operation outside their intended frequency range at elevations above 2,000 feet, which may cause inaccurate pressure readings or signal acquisition problems.
Elekta's Monaco RTP radiation therapy treatment planning software may display inaccurate radiation doses when re-optimizing plans after adding anatomical contours. The defect affects 2,020 units distributed nationwide and internationally.
LetsGetChecked Blood Sample Collection kits were distributed with incorrect shipping labels that assigned samples to wrong users. This could result in incorrect Hepatitis C Virus test results or rejected samples due to demographic mismatches.
St. Jude Medical is recalling the CardioMEMS HF System (Model CM3000) due to excessive radiofrequency emissions that may interfere with pacemakers, defibrillators, and other implanted devices during use. The recall affects 1,905 units distributed worldwide.
Carefusion's CD5 Series Genesis surgical sterilization containers are being recalled due to failure to meet shelf-life testing requirements, resulting in a potential breach of sterility. The recall affects 5,952 devices distributed worldwide.
B. Braun Medical Inc. is recalling Heparin Sodium in Dextrose Injection (Lot J2C017) due to subpotent anti-Factor IIa activity, which may reduce anticoagulant effectiveness.