State

Tennessee product recalls

72,940 recalls have nationwide distribution and so reach Tennessee. 7,819 additional recalls listed Tennessee specifically in their distribution scope.

What the numbers show

Total: 7,819
Critical: 1,317
Severe: 1,653
Most recent: 2026-09-09

Of the 7,819 recalls naming Tennessee we have scored against our rubric, 1,317 (17%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,653 (21%) are Severe.

Which agencies issued them

These figures cover only the 7,819 recalls whose distribution notice names Tennessee specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

2751–2775 of 80759

HighFDA (Devices)·Z-1607-2026·2026-04-01
I.T.S. hand locking plates heat more in MRI than instructions state
I.T.S. GmbH is recalling the HLS Hand Locking Plates System because updated MRI safety testing shows higher RF-induced temperature increases than the Instructions for Use previously reflected.
Product
HLS - Hand Locking Plates System with the below descriptions and corresponding article numbers. 1. Cortical Screw; Article Numbers: 32151-6, 32151-8, 32151-9, 32151-10, 32151-11, 32151-12, 32151-13, 32151-14, 32151-15, 32151-16, 32151-18, 32151-20. 2. HLS Plate, 2 T-Shape
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1630-2026·2026-04-01
Orthalign knee drill plates may allow a bone cut exceeding specification
Orthalign is recalling one lot of the Trimax Pegged Drill Plate for the Lantern Knee System because plates manufactured out of specification can result in a bone cut in excess of 0.0800 inches.
Product
Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 6-7 REF:402567 component Lantern Knee System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1594-2026·2026-04-01
I.T.S. proximal humeral plates heat more in MRI than stated
I.T.S. GmbH is recalling the Humeral Head Plate with Angular Stability because updated MRI safety testing shows higher RF-induced temperature increases than the Instructions for Use previously reflected.
Product
Brand Name: Humeral Head Plate with Angular Stability, with the following description: Proximal Humeral Plate. Article Numbers: 211341-10, 211341-4, 211341-7, 21134-4, 21134-5, 21135-4, 21136-4, 21136-5, 21136-7, 21137-4, 21137-7, 21138-4, 21139-4.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0594-2026·2026-04-01
Ajinomoto Japanese-Style Vegetable Fried Rice Recalled for Glass Contamination
Ajinomoto Foods North America Inc. is recalling Item 5650893 Japanese-Style Vegetable Fried Rice because some packages may contain glass fragments measuring 1–3 cm long and 2–4 mm wide.
Product
Item 5650893 Ajinomoto Japanese-Style Vegetable Fried Rice made with hijiki seaweed, fried tofu, edamame, and other colorful vegetables in an umami dashi sauce Net wt. 17oz. Retail box UPC 071757508934. Product packaging is flexible bags in a master case or flexible bags in cart
Category
Food
Distribution
43 states
HighFDA (Food)·H-0601-2026·2026-04-01
Ajinomoto Vegetable Gyoza Dumplings Recalled for Glass Contamination
Ajinomoto Foods North America Inc. is recalling Ajinomoto Vegetable Gyoza Dumplings due to the presence of glass fragments in the product. The recalled dumplings were distributed nationwide.
Product
Item 6430153 Ajinomoto Vegetable Gyoza Dumplings. Net wt. 24.7oz. per bag. Retail box UPC: 071757010109. Product packaging is flexible bags in a master case or flexible bags in cartons in a master case. There are 8/24.7oz bags or 12.34lb. per case. Case UPC 10071757010106. All
Category
Food
Distribution
43 states
HighFDA (Devices)·Z-1640-2026·2026-04-01
Olympus PK cutting forceps jaws may break from defective welds
Olympus is recalling PK Cutting Forceps because a supplier did not adequately validate the welding process, and defective welds can cause the forceps jaw to break during clinical use.
Product
Brand Name: Olympus PK Cutting Forceps, 5mm 33cm Product Name: PK Cutting Forceps Model/Catalog Number: PK-CF0533 Product Description: An assembly of devices intended to generate and apply radio-frequency (RF) alternating current to soft tissues for cutting and coagulation dur
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·26V207000·2026-04-01
Mack Recalls 2025-2027 Trailers Due to Turn Signal Software Defect
Mack Trucks is recalling 2025-2027 Pioneer and 2027 Anthem trailers because turn signals may not function properly, increasing crash risk.
Product
MACK — MACK PIONEER PR (4), ANTHEM AN (4)
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1644-2026·2026-04-01
Olympus PKS cutting forceps jaws may break from defective welds
Olympus is recalling PKS Cutting Forceps because a supplier did not adequately validate the welding process, and defective welds can cause the forceps jaw to break during clinical use.
Product
Brand Name: Olympus PKS Cutting Forceps, 5mm 33cm Product Name: PKS Cutting Forceps Model/Catalog Number: 920005PK Product Description: The PKS Cutting Forceps are intended to be passed through a 5mm cannula. Coagulation is achieved using electrosurgical energy under visuali
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0596-2026·2026-04-01
Ajinomoto Ling Ling Fried Rice Recalled for Glass Contamination
Ajinomoto Foods North America is recalling Item 81097 Ling Ling Restaurant Style Fried Rice due to glass fragments measuring 1-3 cm long and 2-4 mm wide found in the product. Affected units with Best By dates 9/21/2026 through 3/8/2027 were distributed across 40 U.S. states.
Product
Item 81097 Ajinomoto Ling Ling Restaurant Style Fried Rice Savory Vegetable - A Chinese Style Fried Rice with Edamame, Carrots, Fire Roasted Corn & Red Bell Peppers Prepared with Sweet Soy Sauce Infused Rice. Net wt. 17oz. Retail box UPC 010878810915. Product packaging is flexib
Category
Food
Distribution
43 states
HighFDA (Devices)·Z-1596-2026·2026-04-01
I.T.S. pilon and tibia plates heat more in MRI than stated
I.T.S. GmbH is recalling Pilon Plates with Angular Stability and Anterolateral Tibia Plates because updated MRI safety testing shows higher RF-induced temperature increases than the Instructions for Use reflected.
Product
Pilonplate with Angular Stability, with the below descriptions and corresponding article numbers. 1. Anterolateral Tibia Plate; Article Numbers: 21311-11, 21311-15, 21311-7, 21312-11, 21312-15, 21312-7. 2. Pilon Plate 4mm; Article Numbers: 21094-10, 21094-4, 21094-6, 2109
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1600-2026·2026-04-01
I.T.S. pelvic reconstruction screws heat more in MRI than stated
I.T.S. GmbH is recalling the Pelvic Reconstruction System fixation screw and short spike because updated MRI safety testing shows higher RF-induced temperature increases than the Instructions for Use reflected.
Product
Pelvic Reconstruction System (PRS) with the below descriptions and corresponding article numbers. 1. Fixation Screw; Article Number: 70312. 2. Spike short; Article Number: 70314.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1590-2026·2026-04-01
GE Imactis CT navigation may show needle trajectory that differs from actual
GE Medical Systems is recalling the Imactis CT-Navigation System because of a potential discordance between the simulated needle trajectory and tip position and the actual trajectory and tip position.
Product
Imactis CT-Navigation System, stereotaxic accessory for Computer Tomography (CT), systems, Model Numbers E85101LA and E85101LP
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0600-2026·2026-04-01
Ajinomoto Vegetable Gyoza Dumplings recalled for glass fragments
Ajinomoto Foods North America Inc. is recalling Vegetable Gyoza Dumplings (UPC 071757055483) due to the presence of glass fragments in the product, which could pose a choking or injury hazard if ingested.
Product
Item 6430143 Ajinomoto Vegetable Gyoza Dumplings 12ct. Net wt. 8.92oz. per package. Retail package UPC: 071757055483. Product packaging is flexible bags in a master case or flexible bags in cartons in a master case. There are 20/8.92oz. packages or 11.15 lbs. per case. Carton UP
Category
Food
Distribution
43 states
HighFDA (Food)·H-0592-2026·2026-04-01
Trader Joe's Vegetable Fried Rice recalled for glass fragments
Ajinomoto Foods North America Inc. is recalling Trader Joe's Vegetable Fried Rice (1 lb bags, Item 5650233) due to glass fragments (1–3 cm long, 2–4 mm wide) found in the product. The recall affects approximately 9.9 million pounds distributed across 40 US states.
Product
Item 5650233 Trader Joe's Vegetable Fried Rice, net wt. 1lb per bag. Retail bag UPC 00521482. Product packaging is flexible bags in a master case or flexible bags in cartons in a master case. There are 24/1lb. bags per case. Case UPC 10052148200001. All products are intended t
Category
Food
Distribution
43 states
ModerateFDA (Drugs)·D-0401-2026·2026-04-01
Sodium iodide capsule packs recalled after failing capsule specifications
Radnostix is recalling three lots of the Gelatin Capsule Pack used with the Sodium Iodide I-131 Kit because the product failed tablet and capsule specifications.
Product
SODIUM IODIDE I-131 — SODIUM IODIDE I-131 (SODIUM IODIDE I-131)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1645-2026·2026-04-01
BD Alaris system labeling omits required TLS version for secure Wi-Fi
CareFusion is recalling the BD Alaris System with Guardrails Suite MX because the product labeling does not indicate which TLS version must be enabled on the hospital network for secure Wi-Fi communication.
Product
BD Alaris" System with Guardrails" Suite MX with Point of Care Unit
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1631-2026·2026-04-01
BiDop 3 pocket Doppler labeling includes uncleared fetal indication
Koven Technology is recalling the BiDop 3 Pocket Doppler packaged with a fetal probe because the product labeling includes a fetal indication for use that is not cleared under its 510(k).
Product
Brand Name: BiDop 3 Product Name: BiDop 3 Pocket Doppler (ES-100V3) with BT2M20S8C fetal probe Model/Catalog Number: ES-100V3 (device); BT2M20S8C (2 MHz fetal probe). Software Version: N/A Product Description: Hand-held, battery-powered ultrasonic Doppler blood-flow detector
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1622-2026·2026-04-01
Philips Mini Multi TEE transducer labelling updated to define useful life
Philips is recalling the Mini Multi TEE Ultrasound Transducer to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.
Product
Philips Mini Multi TEE Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1625-2026·2026-04-01
Philips S4-1 ultrasound transducer labelling updated to define useful life
Philips is recalling the S4-1 Ultrasound Transducer to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.
Product
Philips S4-1 Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1620-2026·2026-04-01
Philips L12-5 ultrasound transducer labelling updated to define useful life
Philips is recalling the L12-5 Ultrasound Transducer to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.
Product
Philips L12-5 Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1624-2026·2026-04-01
Philips OMNI III TEE transducer labelling updated to define useful life
Philips is recalling the OMNI III TEE Ultrasound Transducer to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.
Product
Philips OMNI III TEE Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1618-2026·2026-04-01
Philips 3D6-2 ultrasound transducer labelling updated to define useful life
Philips is recalling the 3D6-2 Ultrasound Transducer to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.
Product
Philips 3D6-2 Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1628-2026·2026-04-01
Philips X7-2 ultrasound transducer labelling updated to define useful life
Philips is recalling the X7-2 Ultrasound Transducer to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.
Product
Philips X7-2 Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1621-2026·2026-04-01
Philips L17-5 ultrasound transducer labelling updated to define useful life
Philips is recalling two L17-5 Ultrasound Transducers to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.
Product
Philips L17-5 Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1626-2026·2026-04-01
Philips S5-2 ultrasound transducer labelling updated to define useful life
Philips is recalling one S5-2 Ultrasound Transducer to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.
Product
Philips S5-2 Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide