State

Tennessee product recalls

73,827 recalls have nationwide distribution and so reach Tennessee. 7,860 additional recalls listed Tennessee specifically in their distribution scope.

What the numbers show

Total: 7,860
Critical: 1,324
Severe: 1,974
Most recent: 2026-11-04

Of the 7,860 recalls naming Tennessee we have scored against our rubric, 1,324 (17%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,974 (25%) are Severe.

Which agencies issued them

These figures cover only the 7,860 recalls whose distribution notice names Tennessee specifically. The 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

51376–51400 of 81687

HighFDA (Devices)·Z-0082-2017·2016-10-19
Siemens Rubella IgM Assay Recalled for False Positive Results
Siemens is recalling specific lots of Rubella IgM assays due to increased false positive and indeterminate results.
Product
SIEMENS IMMULITE/IMMULITE 2000 Systems Rubella IgM (RUM), REF/Catalog Number for US: L2KRM2(D), Siemens Material Number (SMN) for US: 10374021, REF/Catalog # for OUS: L2KRM2, SMN for OUS: 10381327; Unique Device Identification Number (UDI) 00630414961996; IVD --- For in vitro…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0070-2017·2016-10-19
Medtronic O-arm O2 Surgical Imaging System Recalled for Calibration Errors
Medtronic is recalling 14 O-arm O2 Surgical Imaging Systems because spatial calibration may be erroneous in navigated images, potentially affecting surgical accuracy.
Product
Medtronic Navigation O-arm O2 Surgical Imaging System Product Catalog Number: BI-700-02000 Product Usage: The O-arm Surgical Imaging System is a multi-dimensional surgical imaging platform that is designed for use in spine, orthopaedic, and trauma-related surgeries. It…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0056-2017·2016-10-19
Gold Standard Baking Recalls Cheese Decadent Danish Due to Metal Shavings
Gold Standard Baking is recalling Cheese Decadent Danish products because they may contain small metal shavings.
Product
Cheese Decadent Danish | NET WT 14 OZ (397g) | Gold Standard Baking, Chicago, IL 60632 | UPC: 087745050019
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0085-2017·2016-10-19
ConMed Recalls HeatWave Electrodes Due to Insulation Damage Risk
ConMed is recalling specific HeatWave Electrodes because damaged shaft insulation could increase the risk of patient burns during arthroscopic procedures.
Product
CONCEPT HEATWAVE Electrode 130 mm x 2.3 mm diameter, REF/Catalog Number CS-023, STERILE, Rx Only Product Usage: The HeatWave Electrode is intended to be used for electro-coagulation of soft tissue in shoulder, ankle, wrist, elbow and knee arthroscopic procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0061-2017·2016-10-19
Archer Farms Strawberry Danish Recalled for Metal Shavings
Gold Standard Baking is recalling Archer Farms Strawberry Danish due to the presence of small metal shavings.
Product
Archer Farms Strawberry Danish | NET WT 14 OZ (397g) | Distributed by Target Corporation Minneapolis, MN 55403 | UPC 085239101094
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0052-2017·2016-10-19
Publix Apple Strip Danish Recalled for Metal Shavings
Gold Standard Baking is recalling Publix Apple Strip Danishes due to the presence of small metal shavings.
Product
Publix Apple Strip Danish | Count, 1 | NET WT 15.00 oz | Distributed by Publix Supermarkets, Inc., Lakeland, FL 33802
Category
Food
Distribution
Distributed nationwide
HighNHTSA·16V757000·2016-10-19
Johnston VT651 and VT801 Street Sweepers Recalled for Hopper Detachment Risk
Johnston is recalling 2013-2016 VT651 and VT801 street sweepers because tipping hinges may crack, allowing the hopper to detach and increase injury risk.
Product
JOHNSTON — JOHNSTON VT801, VT651
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-0057-2017·2016-10-19
Gold Standard Baking Recalls Cherry Decadent Danish Due to Metal Shavings
Gold Standard Baking is recalling Cherry Decadent Danish products due to the presence of small metal shavings. The recall covers 461 cases distributed nationwide.
Product
Cherry Decadent Danish | NET WT 14 OZ (397g) | Gold Standard Baking, Chicago, IL 60632 | UPC: 087745050033
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0062-2017·2016-10-19
Gold Standard Baking Recalls Cheese Danish for Metal Shavings
Gold Standard Baking is recalling The Bakery Cheese Danish sold at Walmart due to the presence of small metal shavings.
Product
The Bakery Cheese Danish | Net Wt 14 OZ (397g) | Distributed By WAL-MART Stores, Inc, Bentonville, AR 72716 | UPC: 605388124487
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0060-2017·2016-10-19
Archer Farms Cheese Danish Recalled for Metal Shavings
Gold Standard Baking is recalling Archer Farms Cheese Danish due to the presence of small metal shavings.
Product
Archer Farms Cheese Danish | NET WT 14 OZ (397g) | Distributed by Target Corporation Minneapolis, MN 55403 | UPC 085239101094
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0080-2017·2016-10-19
Taylor Farms Cranberry Walnut Salad Recalled for Incorrect Allergen Labeling
Taylor Farms is recalling Cranberry Walnut Salad kits because some packages have incorrect labels that fail to declare walnuts or wheat.
Product
Taylor Farms Cranberry Walnut Salad; Salad kit for one: Baby Lettuce Blend, Feta Cheese, Flat Bread Chips, Dried cranberries and Walnuts and Raspberry Vinaigrette dressing. Distributed by: Taylor Farms Inc., Salinas, CA.
Category
Food
Distribution
6 states
HighFDA (Devices)·Z-0074-2017·2016-10-19
Banyan Medical Pyramidal Trocar Recalled for Potential Sterility Issues
Banyan Medical is recalling 5 x 55mm Pyramidal Trocars due to a potential lack of assurance of sterility. The affected units were distributed in Indiana and Tennessee.
Product
Banyan Medical 5 x 55mm Regular Pyramidal Trocar and 2x Cannula. For Laproscopic Use- Sterile Single Use Only. Product Code 400-008
Category
Medical Device
Distribution
2 states
HighFDA (Devices)·Z-0075-2017·2016-10-19
Banyan Medical Pyramidal Tip Trocar Recalled for Sterility Concerns
Banyan Medical is recalling 5 x 55mm Pyramidal Tip Trocars due to a potential lack of assurance of sterility. The recall affects 64 boxes distributed in Indiana and Tennessee.
Product
Banyan Medical 5 x 55mm Pyramidal Tip Trocar w/ 2X Cannula w/ Sideport. Laproscopic Use- Sterile Single Use Only Product Code 400-009
Category
Medical Device
Distribution
2 states
HighFDA (Food)·F-0059-2017·2016-10-19
Kroger Raspberry Danish Strips Recalled for Metal Shavings
Gold Standard Baking is recalling Kroger Raspberry Danish Strips due to the presence of small metal shavings.
Product
Kroger Raspberry Danish Strip, Naturally and Artificially Flavored | NET WT 14 OZ (396g) | Distributed by The Kroger Co., Cincinnati, Ohio 45202 | UPC: 011110836489
Category
Food
Distribution
Distributed nationwide
HighNHTSA·16V756000·2016-10-19
Newmar Recalls 2017 King Aire Motorhomes Due to Radar Mounting Defect
Newmar is recalling 2017 King Aire motorhomes because the collision mitigation radar may be mounted upside down, potentially decreasing performance and increasing crash risk.
Product
NEWMAR — NEWMAR KING AIRE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-0065-2017·2016-10-19
Gold Standard Baking Recalls Apple Crumb Coffee Cake Due to Metal Shavings
Gold Standard Baking is recalling The Bakery Apple Crumb Coffee Cake because it may contain small metal shavings.
Product
The Bakery Apple Crumb Coffee Cake| Net Wt 15 OZ (425g) | Distributed By WAL-MART Stores, Inc, Bentonville, AR 72716 | UPC: 078742052953
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0048-2017·2016-10-19
Pharmedium Heparin Syringes Recalled Due to Potential Loss of Potency
Pharmedium Services, LLC is recalling 240 Heparin Sodium syringes because stability data does not support the expiry date, posing a risk of reduced drug potency.
Product
HEPARIN Sodium Inj., USP, 5,000 USP Heparin Units per 5 mL Total Volume in a syringe, NOT FOR LOCK FLUSH, 1,000 USP Heparin Units per mL, Rx only, PharMEDium, Product code 2K1925.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0071-2017·2016-10-19
Pharmedium Recalls Methadone Syringes Due to Potential Loss of Potency
Pharmedium Services, LLC is recalling 200 syringes of methadone HCl because stability data does not support the expiration dates, posing a risk of reduced drug potency.
Product
methadone HCl, 2.5 mg per 0.5 mL, in 0.9% Sodium Chloride, 0.5 mL Total Volume in a syringe, For IV Use Only, Rx only, PharMEDium, Product code 2T6134.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0084-2017·2016-10-19
Pharmedium Recalls Neostigmine Methylsulfate Syringes Due to Stability Data Concerns
Pharmedium Services, LLC is recalling 700 syringes of neostigmine methylsulfate because stability data does not support the expiration dates, posing a risk of reduced potency.
Product
neostigmine Methylsulfate, 1 mg per mL, 3 mg per 3 mL, 3 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3551.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0047-2017·2016-10-19
Pharmedium Recalls Heparin Sodium Injections Due to Stability Data Concerns
Pharmedium Services, LLC is recalling 399 syringes of Heparin Sodium Injection because stability data does not support the expiration dates, posing a risk of loss of potency.
Product
HEPARIN Sodium Inj. USP, 15,000 USP Heparin Units per 3 mL Injection 3 mL Total Volume in a syringe, Rx only, PharMEDium, Product code 2K1210.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0064-2017·2016-10-19
Winco TMM3 Video-Fluoroscopy Stretcher-Chair Recalled for Non-Conforming Component
Winco Mfg., LLC is recalling 264 TMM3 Series Video-Fluoroscopy Stretcher-Chairs because a non-conforming component caused the arms to no longer meet design specifications.
Product
TransMotion Medical, TMM3 Series Video-Fluoroscopy Swallow Study Stretcher-Chair. Intended use is to provide the caregiver a single platform for receiving, transporting within a facility, performing procedures, recovery and discharge of patients in a monitored outpatient…
Category
Medical Device
Distribution
29 states
ModerateFDA (Drugs)·D-0031-2017·2016-10-19
Pharmedium Recalls ePHEDrine Sulfate Syringes Due to Stability Data Concerns
Pharmedium Services, LLC is recalling 1,545 syringes of ePHEDrine Sulfate because stability data does not support the expiration dates, posing a risk of reduced potency.
Product
ePHEDrine Sulfate, 10 mg per mL, in 0.9% Sodium Chloride, Preservative Free, 1 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3347.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0065-2017·2016-10-19
Winco TMM4 Series Treatment Chair Recalled for Non-Conforming Component
Winco Mfg. is recalling 264 TMM4 Series Multi-Purpose Treatment Chairs because a non-conforming component caused the arms to no longer meet design specifications.
Product
TransMotion Medical, TMM4 Series Multi-Purpose Treatment Chair. Intended use is to provide the caregiver a single platform for receiving, transporting within a facility, performing procedures, recovery and discharge of patients in a monitored outpatient environment.
Category
Medical Device
Distribution
29 states
ModerateFDA (Devices)·Z-0083-2017·2016-10-19
Zimmer Biomet Recalls Phoenix Recon Soft Tissue Sleeve Guide Instruments
Zimmer Biomet is recalling 31 Phoenix Recon Soft Tissue Sleeve Guides due to incompatibility with new revision targeting arms, which may cause surgical delays.
Product
Phoenix Recon Soft Tissue Sleeve Guide, Surgical, Instrument for the sleeve and Orthopedic Manual Surgical Instruments for the Arm Product Usage: The Phoenix Femoral Nail System is to be implanted into the femur for alignment, stabilization and fixation of fractures caused…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0079-2017·2016-10-19
Pharmedium Recalls Morphine Sulfate Syringes Due to Stability Data Concerns
Pharmedium Services, LLC is recalling 21,506 syringes of morphine sulfate because stability data does not support the expiry dates, posing a risk of potency loss.
Product
morphine Sulfate, 1 mg per mL (2 mg per 2 mL), in 0.9% Sodium Chloride, Preservative Free (Contains Sulfites), 2 mL Total Volume in a syringe, For IV use, Rx only, PharMEDium, Product code 2R3259.
Category
Drug
Distribution
Distributed nationwide