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.

8226–8250 of 80943

HighFDA (Devices)·Z-1094-2025·2025-02-12
Philips Azurion and Allura Patient Table Finger Entrapment Risk
Philips Azurion 7 M20 and Allura patient tables pose a finger entrapment risk during manual repositioning. Fingers can get caught between the tabletop and guiding rails, potentially causing finger injury to operators and service personnel.
Product
Azurion 7 M20 System code: (1) 722224 (2) 722079 (3) 722234 (4) 722282 System Code: (1) 722078 (2) 722223 (3) 722233
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 (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-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
HighFDA (Food)·F-0526-2025·2025-02-12
Apple Fritter Donuts Recalled for Potential Listeria Contamination
FGF, LLC is recalling Apple Fritter Donuts (item 8201927) due to potential Listeria monocytogenes contamination. The recall affects 2,017,614 cases distributed nationwide in the US and Canada.
Product
item 8201927 APPLE FRITTER DONUT PFD 70 X 3.5OZ, NET WT 13.78 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1096-2025·2025-02-12
FDA Recalls PROLENE Polypropylene Sutures for Defective Packaging Seals
Ethicon is recalling PROLENE polypropylene sutures because some packages have open seals due to a manufacturing defect. Defective seals may allow pathogens to contaminate the sterile sutures, potentially causing infection.
Product
PROLENE Polypropylene Suture, REF: EH7585H, 8706H, 8833H, 8963H, 8935H PROLENE 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
HighFDA (Drugs)·D-0221-2025·2025-02-12
Potassium Chloride Tablets Recalled for Failed Dissolution Specifications
The FDA is recalling Potassium Chloride Extended-Release Tablets (10 mEq) distributed nationwide because they failed dissolution tests. This could affect how the medication is released in the body.
Product
POTASSIUM CHLORIDE — POTASSIUM CHLORIDE (POTASSIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0517-2025·2025-02-12
FGF Chocolate Cake Rings Recalled for Potential Listeria Contamination
FGF, LLC is recalling 2,017,614 cases of JUST BAKED Chocolate Cake Rings distributed nationwide in the US and Canada due to potential Listeria monocytogenes contamination.
Product
item 8201904 JUST BAKED CHOCOLATE CAKE RINGS ARTIFICIALLY FLAVORED 144x2.5OZ, NET WT 22.5 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0480-2025·2025-02-12
French Crullers Recalled Nationwide for Potential Listeria Contamination
FGF, LLC is recalling French Crullers sold nationwide and in Canada due to potential Listeria monocytogenes contamination. All product with expiration dates from 12/13/24 and earlier is affected.
Product
item 8201812 FRENCH CRULLERS 72x 1.6 OZ, NET WT 6.48 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0465-2025·2025-02-12
FDA Recalls Greenwise Organic Pecan Halves for Undeclared Walnuts
The FDA has recalled Greenwise Organic Pecan Halves (8-ounce bags) due to undeclared walnuts, a major allergen. The affected product was distributed in eight southeastern states.
Product
Greenwise Organic Pecan Halves 8 ounce, plastic printed package marked with lot # 18228 and with a best by date of April.23.2025 stamped on front UPC: 041415212336
Category
Food
Distribution
8 states
HighFDA (Devices)·Z-1076-2025·2025-02-12
Philips Allura CV20 patient tables risk finger entrapment during repositioning
The Philips Allura CV20 System patient tables (AD7 and AD7X models) pose a finger entrapment hazard during manual repositioning. Fingers can become caught between the tabletop and guiding rails, potentially injuring operators and service personnel.
Product
Allura CV20 System Code: 722031
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1118-2025·2025-02-12
Spine Surgery Planning Software Calculation Errors in Rod Planning Parameters
Medicrea International is recalling UNiD Spine Analyzer software due to calculation errors in rod planning parameters. The software experienced anomalies resulting in incorrect values for surgical classification and measurement parameters used in spine surgery planning.
Product
UNiD" Adaptive Spine Intelligence UNiD Spine Analyzer Product Number SW3002 UDI-DI code 03613720286929 Two cloud-based software applications within UNiD Adaptive Spine Intelligence (ASI): the UNiD HUB and the UNiD Spine Analyzer. The UNiD HUB cloud-based software is a he
Category
Medical Device
Distribution
50 states
HighFDA (Food)·F-0508-2025·2025-02-12
FGF LLC Frozen Donuts Recalled for Listeria Contamination Risk
FGF, LLC is recalling BAV CRM BISMARK DONUT frozen donuts nationwide due to potential Listeria monocytogenes contamination. Consumers should not eat the product.
Product
item 8201872 BAV CRM BISMARK DONUT PFD 60x3.85OZ, NET WT 12.99 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0529-2025·2025-02-12
FGF Vanilla Mini Cake Donut Rings Recalled for Listeria Contamination Risk
FGF, LLC is recalling 2,017,614 cases of vanilla mini cake donut rings due to potential Listeria monocytogenes contamination. The affected product was produced on or before December 13, 2024, and distributed nationwide in the US and Canada.
Product
item 8202891 PLAIN VANILLA MINI CAKE DONUT RING BULK 240X1.25OZ, NET WT 16.88 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0507-2025·2025-02-12
ESL Cinnamon Fries Recalled for Potential Listeria Contamination
ESL Cinnamon Fries (item 8201871) produced on December 13, 2024 and prior are being recalled due to potential contamination with Listeria monocytogenes. Approximately 2 million cases were distributed nationwide in the US and Canada.
Product
item 8201871 ESL CINNAMON FRIES 60x3OZ, NET WT 10.13 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0215-2025·2025-02-12
Prescription Carvedilol recalled for manufacturing impurity exceeding FDA specifications
Glenmark Pharmaceuticals is recalling Carvedilol 25 mg tablets nationwide due to a manufacturing quality issue with impurity levels exceeding FDA recommended limits. Multiple lot numbers and expiration dates from February 2025 through February 2026 are affected.
Product
CARVEDILOL — CARVEDILOL (CARVEDILOL)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0519-2025·2025-02-12
FGF Cake Sticks Recalled for Potential Listeria Contamination
FGF cake sticks are being recalled nationwide and in Canada due to potential Listeria monocytogenes contamination. Consumers should not eat the product and should return it to retailers.
Product
item 8201906 JUST BAKED CAKE STICKS 116x2.9 OZ, NET WT 21.03 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0482-2025·2025-02-12
Bavarian Paczki Recalled for Listeria Monocytogenes Contamination Risk
FGF, LLC is recalling Bavarian Paczki (item 8201814) due to potential Listeria monocytogenes contamination. The recall affects 2,017,614 cases distributed nationwide in the US and Canada.
Product
item 8201814 BAVARIAN PACZKI 66x4OZ, NET WT 14.85 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0490-2025·2025-02-12
Frozen Persian Donuts Recalled Due to Listeria Contamination Risk
FGF, LLC is recalling frozen Persian donuts nationwide due to potential Listeria monocytogenes contamination. Consumers should not consume affected products.
Product
item 8201841 GEN PERSIAN DONUT DGH FRZ 168x2OZ, NET WT 18.90 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0510-2025·2025-02-12
FGF Donuts Recalled Nationwide Due to Listeria Contamination Risk
FGF ring donuts recalled nationwide for potential Listeria monocytogenes contamination. The recall covers 2,017,614 cases produced through December 13, 2024.
Product
item 8201879 RING RND DONUT ZGT PDF 96x2.25 OZ, NET WT 12.15 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0479-2025·2025-02-12
Sour Cream Cake Donuts Recalled for Potential Listeria Contamination
FGF, LLC is recalling Old Fashioned Sour Cream Cake Donuts due to potential Listeria monocytogenes contamination. The recall affects 2,017,614 cases distributed nationwide in the US and Canada.
Product
item 8201811 OLD FASHIONED NATURALLY AND ARTIFICIALLY FLAVORED SOUR CREAM CAKE DONUTS 90x2.5 OZ, NET WT 12.66 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1084-2025·2025-02-12
Philips Allura and Azurion Patient Tables Recall Due to Finger Entrapment Risk
Philips is recalling AD7 and AD7X patient tables used in Allura and Azurion medical imaging systems due to a finger entrapment hazard during manual repositioning. Operators and service personnel are at risk of finger injury.
Product
AlluraXperFD20/10 System Code: (1) 722029
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1085-2025·2025-02-12
Finger entrapment hazard in Philips Allura fluoroscopy patient tables
Philips is recalling AD7 and AD7X patient tables from Allura and Azurion fluoroscopy systems. During manual repositioning, fingers can become trapped between the guiding rails and tabletop, potentially causing injury.
Product
Allura Xper FD20/20 System Code: (1) 722038
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0481-2025·2025-02-12
FGF Donuts Recalled for Potential Listeria Contamination
FGF, LLC is recalling dual-filled chocolate and Bavarian yeast ring donuts due to potential Listeria monocytogenes contamination. The recall affects 2,017,614 cases distributed in the US and Canada.
Product
item 8201813 DUAL FILLED NATURALLY & ARTIFICIALLY FLAVORED CHOCOLATE AND BAVARIAN FILLED YEAST RING DONUT 80x3.1OZ, NET WT 13.97 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1088-2025·2025-02-12
Philips Azurion Patient Tables Recalled for Finger Entrapment Risk
Philips Azurion patient tables used in medical imaging systems can trap fingers between the tabletop and rails during manual repositioning, potentially causing finger injury to operators and service personnel.
Product
Azurion 3 M15 System Code: (1) 722064 (2) 722222 (3) 722280
Category
Medical Device
Distribution
Distributed nationwide