State

Tennessee product recalls

73,092 recalls have nationwide distribution and so reach Tennessee. 7,851 additional recalls listed Tennessee specifically in their distribution scope.

What the numbers show

Total: 7,851
Critical: 1,327
Severe: 1,665
Most recent: 2026-09-23

Of the 7,851 recalls naming Tennessee we have scored against our rubric, 1,327 (17%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,665 (21%) are Severe.

Which agencies issued them

These figures cover only the 7,851 recalls whose distribution notice names Tennessee specifically. The 73,092 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

8201–8225 of 80943

HighFDA (Devices)·Z-1115-2025·2025-02-12
Beckman Coulter DxI 9000 immunoassay analyzer recalled for software-related motion errors
Beckman Coulter is recalling 61 DxI 9000 immunoassay analyzers worldwide due to a software error causing tray gripper motion errors that result in intermittent hard stops and delays in patient test results.
Product
Beckman Coulter DxI 9000 Access Immunoassay Analyzer, catalog number C11137; in-vitro diagnostic instrument
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1082-2025·2025-02-12
Philips AlluraXper FD20 operating room surgical table finger entrapment risk
Philips AlluraXper FD20 operating room tables can trap fingers during manual repositioning, risking injury. The hazard affects both operators and service personnel worldwide.
Product
AlluraXper FD20 Biplane OR Table System Code: (1) 722020 (2) 722025
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0499-2025·2025-02-12
FGF Sour Cream Cake Donuts Recalled Due to Listeria Contamination Risk
FGF's Just Baked Sour Cream Cake Donuts are being recalled nationwide due to potential Listeria monocytogenes contamination. Approximately 2 million cases produced on or before December 13, 2024 are affected.
Product
item 8201860 JUST BAKED SOUR CREAM CAKE DONUTS 120x2.5 OZ, NET WT 18.75 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0520-2025·2025-02-12
Yeast Donuts Recalled for Potential Listeria Contamination
FGF, LLC is recalling yeast donuts nationwide and in Canada due to potential Listeria monocytogenes contamination. Consumers should not consume affected products.
Product
item 8201919 BAR YST DONUT UNFLD PFD 74x3OZ, NET WT 12.49 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0500-2025·2025-02-12
Just Baked Eclairs Recalled Nationwide Due to Listeria Contamination Risk
FGF, LLC is recalling Just Baked Eclairs nationwide in the US and Canada due to potential Listeria monocytogenes contamination. All products produced on 12/13/24 or earlier are affected.
Product
item 8201863 JUST BAKED ECLAIRS 84x2.36 OZ, NET WT 12.39 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0524-2025·2025-02-12
Donut Product Recalled for Potential Listeria Monocytogenes
FGF, LLC is recalling approximately 2 million cases of its BAV CRM BAR DONUT product nationwide due to potential Listeria monocytogenes contamination. Consumers should not consume the product and should dispose of it or return it to the retailer.
Product
item 8201923 BAV CRM BAR DONUT PFD 78 X 3OZ, NET WT 13.16 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1113-2025·2025-02-12
Sysmex PS-10 Sample Preparation System Recalled for False Test Results
Sysmex PS-10 Sample Preparation Systems may produce false test results due to sporadic omission of the probe wash step during antibody pipetting. Thirty-two units have been recalled nationwide.
Product
Sysmex PS-10 Sample Preparation System with software version 1.5 and 1.6., Catalog Number BQ716341. Product usage for automated pipetting, diluting, and specimen processing workstations for flow cytometric analysis.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0470-2025·2025-02-12
Cake Donut Rings Recalled for Potential Listeria Contamination
FGF, LLC is recalling cake donut rings due to potential contamination with Listeria monocytogenes. Distribution included nationwide US and Canada.
Product
item 8201779 GEN PLN CAKE DONUT RINGS PFD 90x2.5 OZ, NET WT 12.66LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0458-2025·2025-02-12
Monkey Spit BBQ Sauce recalled due to undeclared soy allergen
Monkey Spit 'Swamp Mop' BBQ Sauce is being recalled because it contains an undeclared soy allergen in a sub-ingredient. The product was distributed through local markets and online sales nationwide.
Product
Monkey Spit "Swamp Mop" BBQ Sauce, 12 fl oz (355ml) glass bottle, 12 bottles/case; Refrigerate after opening; Monkey Spit, LLC, Tepusquet Cyn Santa Maria, CA 93454; Manufactured by Smith House MFG. 146-A S. Thompson Ave. Nipomo, CA 93444 (805) 619.7959 UPC#8 54540 00230 3
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0494-2025·2025-02-12
Frozen donuts recalled nationwide for potential listeria contamination
FGF, LLC is recalling frozen donuts nationwide due to potential contamination with listeria monocytogenes. Affected products were produced on or before December 13, 2024.
Product
item 8201845 GEN RG HEX DONUT DGH FRZ 144x1.88OZ, NET WT 15.23 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0460-2025·2025-02-12
Monkey Spit BBQ Sauce recalled for undeclared milk allergen
Monkey Spit Monkey Mop BBQ Sauce is recalled because it contains undeclared milk from butter, a common allergen. Consumers with milk allergies should not consume this product.
Product
Monkey Spit "Monkey Mop" BBQ Sauce, 12 fl oz (355ml) glass bottle, 12 bottles/case; Refrigerate after opening; Manufactured by Smith House MFG. 146-A S. Thompson Ave. Nipomo, CA 93444 (805)619-7959 Monkey Spit, LLC, UPC#8 54540 00206 8
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1044-2025·2025-02-12
Medical X-Ray System Permits Bypass of Radiation Exposure Control
GE Medical Systems' Discovery XR656HD X-Ray imaging systems can allow radiation exposures to exceed the Automatic Exposure Control limit without blocking further exposure. Approximately 3,149 units are affected worldwide, including 1,697 in the United States.
Product
Discovery XR656HD. X-Ray imaging system.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1045-2025·2025-02-12
GE Discovery XR656 HD X-ray system AEC control malfunctions during imaging
GE Medical Systems is recalling the Discovery XR656 HD X-ray imaging system due to a malfunction in the Automatic Exposure Control (AEC) feature. The defect allows continued X-ray exposure beyond intended limits without requiring operator acknowledgment.
Product
Discovery XR656 HD. X-Ray imaging system.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1114-2025·2025-02-12
Endodontic Files Recalled for Excess Irradiation Causing Package Integrity Issues
US Endodontics is recalling endodontic files due to irradiation above specification, which may compromise package integrity. The recall affects 789,729 devices distributed in the US and internationally.
Product
Brasseler ESR Rotary/Reciprocating Endodontic File Device SKU AP120213PK AP120253PK AP120313PK AP125213PK AP125253PK AP125313PK AP135213PK AP135253PK AP135313PK AP145213PK AP145253PK AP145313PK AP1GP213PK AP1GP253PK AP1GP313PK O.U.S. Products: EdgeFile X7 REF
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0516-2025·2025-02-12
Apple Cider Cake Rings Recalled for Potential Listeria Contamination
FGF, LLC is recalling Just Baked Apple Cider Cake Rings due to potential Listeria monocytogenes contamination. Approximately 2,017,614 cases were distributed nationwide in the US and Canada.
Product
item 8201901 JUST BAKED APPLE CIDER CAKE RINGS WITH NATURAL FLAVORS 144x2.5OZ, NET WT 22.5 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1093-2025·2025-02-12
Philips Azurion patient tables recalled for finger entrapment risk
Philips is recalling Azurion 7 M12 and Allura patient tables used in medical imaging systems due to a finger entrapment hazard during manual repositioning. Operators and service personnel may suffer finger injury if fingers are caught between the tabletop and guiding rails.
Product
Azurion 7 M12 System Code: (1) 722078 (2) 722223 (3) 722233
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1097-2025·2025-02-12
PERMA-HAND Silk Sutures Recalled for Packaging Sterility Breach
Ethicon is recalling PERMA-HAND Silk Sutures that may have open seals on packaging due to manufacturing defects, risking sterility compromise and patient infection. Approximately 78,792 units were distributed nationwide and internationally.
Product
PERMA-HAND Silk Suture, REF: K872H, W723H, 623H, K833H; Perma-hand Silk Suture is indicated for use in general soft tissue approximation and/or ligation, including use in cardiovascular, ophthalmic and neurosurgical procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V081000·2025-02-12
Volkswagen Atlas transmissions may have been manufactured incorrectly
Volkswagen is recalling certain 2025 Atlas and Atlas Cross Sport vehicles because the transmission may have been manufactured incorrectly, which can result in a loss of drive power.
Product
VOLKSWAGEN — VOLKSWAGEN ATLAS CROSS SPORT, ATLAS
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1111-2025·2025-02-12
Temporary Titanium Abutments May Fracture in Dental Implants
DDS Lab temporary titanium abutments may have been installed in some dental implant restoration cases instead of definitive abutments. The components may fracture, risking restoration loosening, oral tissue injury, and aspiration.
Product
Temporary Titanium Abutments
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V078000·2025-02-12
Porsche Recalls 2023 911 Models Due to Rear Seat Belt Bolt Issue
Porsche is recalling 2023 911 vehicles because rear seat belt buckle bolts may not be tightened properly, which could reduce occupant restraint during a crash.
Product
PORSCHE — PORSCHE 911
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V082000·2025-02-12
Volkswagen Tiguan camera control units may error at vehicle startup
Volkswagen is recalling certain Tiguan, Arteon and Audi Q3 vehicles because a camera control unit error at startup may prevent the rearview image displaying.
Product
VOLKSWAGEN — VOLKSWAGEN, AUDI TIGUAN, ARTEON, Q3
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-0497-2025·2025-02-12
Just Baked Yeast Shells recalled for potential Listeria contamination
FGF, LLC is recalling Just Baked Yeast Shells due to potential Listeria monocytogenes contamination. The recall affects 2,017,614 cases distributed nationwide in the US and Canada.
Product
item 8201858 JUST BAKED YEAST SHELLS 120x1.88 OZ, NET WT 14.10 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0515-2025·2025-02-12
Apple Fritter Donuts Recalled for Potential Listeria Contamination
FGF, LLC is recalling apple fritter donuts nationwide due to potential Listeria monocytogenes contamination. Consumers should not consume affected products.
Product
item 8201900 APPLE FRITTER DONUT ZGT PFD 54x3OZ, NET WT 9.11 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0505-2025·2025-02-12
FGF Twist Donuts Recalled Due to Listeria Contamination Risk
FGF's Twist Donuts are being recalled nationwide in the US and Canada due to potential Listeria monocytogenes contamination. The recall affects approximately 2 million cases produced on or before December 13, 2024.
Product
item 8201868 GEN TWIST DONUT ZGT PFD 84x1.75 OZ, NET WT 12.93 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1086-2025·2025-02-12
Philips AD7 and AD7X Patient Table Finger Entrapment Risk
The Philips AD7 and AD7X patient tables pose a finger entrapment risk during manual repositioning. Operators and service personnel could sustain finger injuries from the gap between the longitudinal guiding rails and tabletop.
Product
AlluraXperFD20/15 System Code: (1) 722058
Category
Medical Device
Distribution
Distributed nationwide