State

Tennessee product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

40426–40450 of 81669

ModerateFDA (Devices)·Z-0150-2019·2018-10-24
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Packaging Issues
Zimmer Biomet is recalling 33 Affixus Hip Fracture Nails because sterile packaging was found open during surgery. The devices were distributed nationwide and in Chile and the Netherlands.
Product
Affixus Hip Fracture Nail Left 125 11 mm x 260 mm, Item Number 814411260 Product Usage: Intended for the fixation of fractures
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0059-2019·2018-10-24
Product Quest Recalls Best Choice Saline Nasal Spray for Quality Deviations
Product Quest Manufacturing LLC is recalling Best Choice Saline Nasal Spray because it was manufactured under conditions that could impact product quality.
Product
Best Choice, SALINE Nasal Spray (Sodium Chloride 0.65% Phenylcarbinol & Benzalkonium Chloride as Preservatives), 1.5 FL OZ (44 mL) bottle, Proudly Distributed By: Valu Merchandisers, Co., 5000 Kansas Ave, Kansas City, KS 66106, UPC 0 70038 58487 2.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0117-2019·2018-10-24
Siemens Atellica IM CKMB Master Curve Material Recalled for Potential Bias
Siemens Healthcare Diagnostics is recalling Atellica IM CKMB Master Curve Material due to a potential bias identified when compared to internal standards.
Product
Atellica IM CKMB Master Curve Material, Cat No. 10995534 Product Usage: For in vitro diagnostic use for evaluating the ADVIA Centaur CKMB assay. This material is intended to be run singly as unknown samples after a two-point calibration has been performed on the system.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0075-2019·2018-10-24
Rhinall Nasal Decongestant Spray Recalled for Manufacturing Quality Deviations
Product Quest Manufacturing LLC is recalling Rhinall Nasal Decongestant Nasal Spray due to manufacturing conditions that could impact product quality.
Product
Rhinall Nasal Decongestant Nasal Spray (phenylephrine HCl), 0.25%, 1 1/3 Fl Oz. (40 ml), Manufactured for: Scherer Laboratories, Inc., Atlanta, GA 30339.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0158-2019·2018-10-24
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Packaging Defects
Zimmer Biomet is recalling 85 Affixus Hip Fracture Nails because sterile packaging was found open during surgery. The recall covers units distributed in the US and abroad.
Product
Affixus Hip Fracture Nail 130 11 mm x 180 mm, Item Number 814511180 Product Usage: Intended for the fixation of fractures
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0113-2019·2018-10-24
Siemens Recalls ADVIA Centaur CKMB Calibrator Kits Due to Potential Bias
Siemens Healthcare Diagnostics is recalling 1,870 ADVIA Centaur CKMB Calibrator kits due to a potential bias compared to internal standards.
Product
ADVIA Centaur CKMB Calibrator, Cat No. 09318028 Product Usage: For in vitro diagnostic use in calibrating ADVIA Centaur systems CKMB assays.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0049-2019·2018-10-24
QC Quality Choice Saline Nasal Gel Recalled for Quality Deviations
Product Quest Manufacturing LLC is recalling QC Quality Choice Saline Nasal Gel with Soothing Aloe due to manufacturing deviations that could impact product quality.
Product
QC Quality Choice, Saline Nasal Gel with Soothing Aloe, 0.5 OZ (14.1 g) tube, Distributed by C.D.M.A., Inc., 43157 W. Nine Mile, Novi, MI 48376-0995, UPC 6 35515 99202 3.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0076-2019·2018-10-24
Rexall Sinus Nasal Pump Mist Recalled for Quality Control Issues
Product Quest Manufacturing LLC is recalling Rexall Sinus Nasal Pump Mist due to manufacturing deviations that could impact product quality.
Product
Rexall, Sinus Nasal Pump Mist, (Oxymetazoline Hydrochloride 0.05%), 1 FL OZ (30mL) bottle, SKU 00744201
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0024-2019·2018-10-24
Humco Recalls Thyroid Powder Due to Inconsistent Active Ingredient Levels
Humco Holding Group, Inc. is recalling 10 kilograms of Thyroid, USP powder because it has inconsistent levels of levothyroxine and liothyronine.
Product
Thyroid, USP (Full Strength) Levothyroxine 112.1 mcg/grain Liothyronine 29.2 mcg/grain Active Pharmaceutical Ingredient Rx Only 1000 grams NDC 0395-6580-43 Packaged by: Humco Texarkana, TX 75501 USA
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0051-2019·2018-10-24
Rite Aid Nasal Spray Recalled for Manufacturing Quality Deviations
Product Quest Manufacturing LLC is recalling Rite Aid nasal spray due to manufacturing conditions that could impact product quality.
Product
Rite Aid Pharmacy, nasal relief NO DRIP PUMP SPRAY nasal spray, (oxymetazoline hydrochloride 0.05%), 12 Hour, 1 FL OZ (30 mL) bottle, Distributed By: Rite Aid, 30 Hunter Lane, Camp Hill, PA 17011, UPC 0 11822 31412 1.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0126-2019·2018-10-24
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Packaging Defects
Zimmer Biomet is recalling 51 Affixus Hip Fracture Nails because sterile packaging was found open during surgery.
Product
Affixus Hip Fracture Nail Right 125 9 mm x 340 mm, Item Number 814309340 Product Usage: Intended for the fixation of fractures
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0031-2019·2018-10-24
Tropical Nut & Fruit Company Recalls United Fitness Mix Due to Maggots
Tropical Nut & Fruit Company is recalling United Fitness Mix 25LB boxes after a customer reported finding maggots in the product.
Product
United Fitness Mix 25LB box, Almonds, Walnuts, Pumpkin Seeds, Cashews, Blueberries***Manufactured or packed in a facility that uses tree nuts, peanuts, milk, soy, and wheat products" Distributed by: Truly Good Foods, Orlando, FL 32811 UPC 0 94154 00803 7
Category
Food
Distribution
1 state
ModerateFDA (Devices)·Z-0142-2019·2018-10-24
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Packaging Issues
Zimmer Biomet is recalling nine Affixus Hip Fracture Nails because complaints indicated the sterile packaging was already open when the products were opened in surgery.
Product
Affixus Hip Fracture Nail Right 125 13 mm x 360 mm, Item Number 814313360 Product Usage: Intended for the fixation of fractures
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0192-2019·2018-10-24
Siemens Atellica IM 1300 Analyzer Software Recall for Behavioral Issues
Siemens Healthcare Diagnostics is recalling Atellica IM 1300 Analyzers with software version 1.13 and lower due to five identified behavioral issues affecting reagent locks, barcode reading, and result reporting.
Product
Atellica IM 1300 Analyzer (SMN 11066001). The Atellica" Solution is a multi-component system for in vitro diagnostic testing of clinical specimens.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0151-2019·2018-10-24
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Packaging Defect
Zimmer Biomet is recalling 15 Affixus Hip Fracture Nails because sterile packaging was found open during surgery. The recall covers US and foreign distribution.
Product
Affixus Hip Fracture Nail Left 125 11 mm x 320 mm, Item Number 814411320 Product Usage: Intended for the fixation of fractures
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0023-2019·2018-10-24
Humco Recalls Thyroid Powder Due to Inconsistent Active Ingredient Levels
Humco Holding Group, Inc. is recalling Thyroid, USP (Porcine) powder because it has inconsistent levels of levothyroxine and liothyronine.
Product
Thyroid, USP (Porcine) Levothyroxine 36.3 mcg/grain Liothyronine 9.7 mcg/grain Active Pharmaceutical Ingredient Rx Only 100 grams NDC 0395-8077-62 Packaged by: Humco Texarkana, TX 75501 USA
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0136-2019·2018-10-24
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Packaging Issues
Zimmer Biomet is recalling 20 Affixus Hip Fracture Nails because complaints indicated the sterile packaging was already open when the product was opened in surgery.
Product
Affixus Hip Fracture Nail Right 125 11 mm x 440 mm, Item Number 814311440 Product Usage: Intended for the fixation of fractures
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0137-2019·2018-10-24
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Packaging Issues
Zimmer Biomet is recalling 18 Affixus Hip Fracture Nails because complaints indicated the sterile packaging was already open when the product was opened in surgery.
Product
Affixus Hip Fracture Nail Right 125 11 mm x 460 mm, Item Number 814311460 Product Usage: Intended for the fixation of fractures
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0109-2019·2018-10-24
FDA Recalls Ambu Aura40 Reusable Laryngeal Masks Due to Labeling Error
Besmed Health Business Corporation is recalling Ambu Aura40 Standard reusable laryngeal masks because they are packaged in pouches marked as single-use.
Product
Ambu Aura40 Standard, Reusable Laryngeal Mask Catalog Number: 340300000
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0167-2019·2018-10-24
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Packaging Defect
Zimmer Biomet is recalling 16 Affixus Hip Fracture Nails because sterile packaging was found open during surgery. The recall covers units distributed in the US and abroad.
Product
Affixus Hip Fracture Nail Left 130 11 mm x 400 mm, Item Number 814611400 Product Usage: Intended for the fixation of fractures
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0064-2019·2018-10-24
Walgreens Severe Anefrin Nasal Spray Recalled for Quality Deviations
Product Quest Manufacturing LLC is recalling Walgreens NO DRIP Severe Anefrin Nasal Spray due to manufacturing deviations that could impact product quality.
Product
Walgreens, NO DRIP Severe Anefrin Nasal Spray (Oxymetazoline HCl 0.05%) Nasal Decongestant, Maximum Strength, 12 Hour + Menthol, 0.5 FL OZ (15 mL) bottle, Distributed By: Walgreen Co., 200 Wilmot Rd., Deerfield, IL 60015, NDC 0363-7001-01, UPC 3 11917 18536 1.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0176-2019·2018-10-24
Terumo Advanced Perfusion System 1 Electronic Patient Gas System Recall
Terumo is recalling 152 Advanced Perfusion System 1 Electronic Patient Gas Systems because the service manual was not updated for software version 1.30.
Product
Terumo¿ Advanced Perfusion System 1 Electronic Patient Gas System, Catalog#: 801188
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0119-2019·2018-10-24
Cypress Medical Recalls McKesson Insulin Syringes Due to Suction Defect
Cypress Medical Products LLC is recalling 400 cases of McKesson Insulin Syringes because a small hole impedes liquid suction.
Product
McKesson Insulin Syringe 0.3mL 31GX5/16 Item Numbers: 102-SN310C31516P Product Usage: Indication of Use: Injection of U-100 insulin only.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0169-2019·2018-10-24
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Packaging Defect
Zimmer Biomet is recalling 20 Affixus Hip Fracture Nails because sterile packaging was found open during surgery. The recall covers units distributed in the US and abroad.
Product
Affixus Hip Fracture Nail 125 9 mm x 165 mm, Item Number 816709165 Product Usage: Intended for the fixation of fractures
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0145-2019·2018-10-24
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Packaging Defects
Zimmer Biomet is recalling 16 Affixus Hip Fracture Nails because sterile packaging was found open during surgery. The recall covers units distributed in the US and two foreign countries.
Product
Affixus Hip Fracture Nail Left 125 9 mm x 260 mm, Item Number 814409260 Product Usage: Intended for the fixation of fractures
Category
Medical Device
Distribution
Distributed nationwide