State

Tennessee product recalls

73,509 recalls have nationwide distribution and so reach Tennessee. 7,853 additional recalls listed Tennessee specifically in their distribution scope.

What the numbers show

Total: 7,853
Critical: 1,327
Severe: 1,970
Most recent: 2026-10-14

Of the 7,853 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 1,970 (25%) are Severe.

Which agencies issued them

These figures cover only the 7,853 recalls whose distribution notice names Tennessee specifically. The 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

23326–23350 of 81362

SevereFDA (Drugs)·D-0740-2022·2022-03-30
Hand Sanitizer Isopropyl Alcohol Recall Due to Methanol Contamination
Tennessee Technical Coatings is recalling hand sanitizer products due to CGMP deviations. Certain lots were manufactured under the same conditions as a product lot found to contain methanol.
Product
HAND SANITIZER Isopropyl Alcohol Antiseptic 75%, Net contents: 1 U.S. Gallon/3.785 Liters Tennessee Technical Coatings Corporation, 1421 Higgs Road (P.O. Box 1698) Lewisburg, TX 37091, NDC 76921-000-01
Category
Drug
Distribution
2 states
HighFDA (Devices)·Z-0823-2022·2022-03-30
NuOss Collagen Blocks Recalled Due to Product Substitution Error
Ace Surgical Supply is recalling NuOss Collagen Blocks because some units were mistakenly packaged with Collatene Fibrillar Collagen instead, which may result in suboptimal bone repair during dental and maxillofacial procedures.
Product
NuOss Collagen Block Size 8mm x 9mm x 9mm- used in filling periodontal and maxillofacial defects. Catalog Number: 5099250
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0821-2022·2022-03-30
Medical Device Air Supply Unit Recalled for Potential Electrical Shock Hazard
Baxter Healthcare is recalling the Compella Therapy Air Supply Unit due to potential power cord damage that could expose electrical conductors and create a shock risk. The recall affects 6,022 units distributed worldwide.
Product
Compella Therapy Air Supply Unit
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V206000·2022-03-30
2022 Keystone Passport Travel Trailers Recalled for Incorrect Axles and Tires
Keystone RV Company is recalling 2022 Passport travel trailers equipped with incorrect size axles and tires that could cause overloading. Dealers will replace the suspension components free of charge.
Product
KEYSTONE — KEYSTONE PASSPORT
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0717-2022·2022-03-30
Eye Lubricant Drops Recalled for Insufficient Sterility Assurance
Akorn, Inc. is recalling 62,331 boxes of TheraTears Extra lubricant eye drops distributed nationwide due to lack of assured sterility. Non-sterile eye drops could pose infection risks.
Product
THERATEARS EXTRA — THERATEARS EXTRA (CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0683-2022·2022-03-30
Fluocinonide Cream Recalled for Manufacturing Compliance and Stability Deviations
Teligent Pharma, Inc. is recalling Fluocinonide Cream USP 0.1% due to manufacturing compliance deviations and discontinuation of stability studies. The recall affects products nationwide in the USA and Puerto Rico.
Product
Fluocinonide Cream USP, 0.1%, 120 grams tube, Rx Only, Manufactured by: Teligent Pharma, Inc., Buena, New Jersey 08310, NDC 52565-079-11.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0719-2022·2022-03-30
FDA Recalls NAD+ Injection Due to Sub-Potency and Stability Concerns
Olympia Compounding Pharmacy is recalling NAD+ Nicotinamide Adenine Dinucleotide injection vials nationwide due to sub-potency or exceeded reconstitution time.
Product
NAD+ Nicotinamide Adenine Dinucleotide, Lyophilized powder for reconstitution, Multi-Dose 500 mg per vial, Each ML contains: 0.288% Sodium Phosphate Monobasic USP, 0.42% Sodium Phosphate Dibasic USP, 5% Mannitol USP, Sterile Water for Injection USP, Rx Only, Olympia…
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0817-2022·2022-03-30
Codman Cranial Access Kits Recalled Due to Incorrect Expiration Dates on Labels
Integra LifeSciences is recalling 1,161 Codman Cranial Access Kits due to incorrect expiration dates on the outer box labels. Using the product past its correct expiration date may cause pain, infection, or adverse tissue reaction.
Product
Codman Cranial Access Kits- indicated when a craniotomy is required for placement of an intracranial pressure (ICP) monitoring device and/or cerebrospinal fluid drainage procedures. Product umber: 826614
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0818-2022·2022-03-30
Codman Cranial Access Kits Recall: Incorrect Expiration Dates on Labels
Integra LifeSciences is recalling Codman Cranial Access Kits due to incorrect extended expiration dates printed on outer box labels. Using expired kits may result in pain, infection, or adverse tissue reaction.
Product
Codman Cranial Access Kits- indicated when a craniotomy is required for placement of an intracranial pressure (ICP) monitoring device and/or cerebrospinal fluid drainage procedures. Part Number: 826616
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0813-2022·2022-03-30
Outset Tablo Hemodialysis Console Recalled for Heat Damage Risk
Outset Medical is recalling Tablo hemodialysis consoles (models PN-0003000 and PN-0006000) nationwide due to a component that may cause heat-related damage to the device.
Product
Outset Tablo Console Model Number: PN-0003000 Model Number: PN-0006000
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0820-2022·2022-03-30
Compella Bariatric Bed System Recall—Power Cord Electrical Shock Risk
Baxter Healthcare is recalling the Compella Bariatric Bed System due to potential power cord damage that could expose electrical conductors, creating a shock hazard. Approximately 5186 units worldwide are affected.
Product
Compella Bariatric Bed System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0706-2022·2022-03-30
Norepinephrine Bitartrate Injection Recalled Due to Defective Container
Athenex Pharma Solutions is recalling Norepinephrine Bitartrate Injection due to defective containers affecting specific lots distributed nationwide.
Product
Norepinephrine Bitartrate Injection 4mg per 250 mL in 0.9% Sodium Chloride, 4 mg, 250 mL excel bag, Rx only, Athenex Pharma Solutions, LLC, Clarence, NY, 14031, NDC 76154-474-15
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0669-2022·2022-03-30
FDA Recalls Betamethasone Dipropionate Lotion Due to Manufacturing Deviations
Teligent Pharma is recalling Betamethasone Dipropionate Lotion due to manufacturing practice deviations and discontinuation of the stability study program. The recall affects 43,218 bottles distributed nationwide.
Product
Betamethasone Dipropionate Lotion USP, 0.05%* (Augmented), packaged in a) 30 mL (29 grams) bottles, NDC 52565-023-29; b) 60 mL (58 grams) bottles, NDC 52565-023-59, Rx Only, Teligent Pharma, Inc., Buena, NJ 08310
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0734-2022·2022-03-30
Azurion Medical Imaging System Software Defect Affects Patient Dose Control
Philips Azurion R2.1 systems have a software defect that causes the Patient Type to change unexpectedly when starting a procedure, potentially affecting dose control settings without user notification.
Product
Azurion systems with software release R2.0.x
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0681-2022·2022-03-30
Diflorasone Diacetate Ointment recalled due to discontinued stability studies
Teligent Pharma is recalling all unexpired Diflorasone Diacetate Ointment 0.05% due to cGMP deviations. The company discontinued its stability study program, preventing verification that the product maintains safety and effectiveness throughout shelf life.
Product
Diflorasone Diacetate Ointment USP, 0.05%, Net Wt 60 g tubes, Rx only, Manufactured for: SOLA Pharmaceuticals, LLC Baton Rouge, LA 70809, NDC 70512-031-60.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0678-2022·2022-03-30
Desoximetasone Ointment USP Recalled by Teligent Pharma
Teligent Pharma is recalling Desoximetasone Ointment USP 0.25% in all sizes nationwide due to cGMP deviations related to discontinuation of the stability study program.
Product
Desoximetasone Ointment USP, 0.25%, packaged in a) 100 grams tubes, NDC 52565-030-99; b) 60 grams tubes, NDC 52565-030-60; c) 15 grams tubes, NDC 52565-030-15, Rx Only, Teligent Pharma, Inc., Buena, New Jersey 08310.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0702-2022·2022-03-30
Gentamicin Sulfate Cream Recalled Due to Manufacturing Practice Violations
Teligent Pharma, Inc. is recalling 31,489 tubes of Gentamicin Sulfate Cream (0.1%) nationwide due to manufacturing violations. The company discontinued its stability testing program without proper authorization.
Product
Gentamicin Sulfate Cream USP, 0.1%, packaged in 30 grams tubes, Rx Only, Manufactured for: SOLA Pharmaceuticals, LLC, Baton Rouge, LA 70810, NDC 70512-036-30.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0676-2022·2022-03-30
Desoximetasone Ointment USP 0.05% Recalled Due to cGMP Deviations
Teligent Pharma is recalling Desoximetasone Ointment USP 0.05% nationwide due to current good manufacturing practice (cGMP) deviations. The firm is discontinuing its stability study program, affecting all products within expiry.
Product
Desoximetasone Ointment USP, 0.05%, Net Wt. 100 grams tubes, Rx only, Manufactured for: SOLA Pharmaceuticals, Baton Rouge, LA 70810, NDC 70512-037-10.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0704-2022·2022-03-30
Lidocaine Cream 4% Recalled Due to Manufacturing Quality Deviations
Teligent Pharma is recalling all unexpired batches of Lidocaine Cream 4% (30-gram tubes) nationwide because the company is discontinuing its stability study program, a violation of manufacturing standards.
Product
Lidocaine Cream 4%, Net Wt. 30 grams tube, Distributed by: RUGBY LABORATORIES, 17177 N. Laurel Park Dr., Suite 233, Livonia, MI 48152, NDC 0536-1281-28.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0697-2022·2022-03-30
Triamcinolone Acetonide Cream USP 0.1% Recall — Stability Study Discontinuation
Teligent Pharma is recalling all unexpired Triamcinolone Acetonide Cream USP 0.1% nationwide due to discontinuation of its stability study program, which creates a cGMP deviation. The company has recalled approximately 721,225 tubes and 90,893 jars distributed across multiple package sizes.
Product
Triamcinolone Acetonide Cream USP, 0.1%, packaged in a) 15 grams tubes, NDC 52565-056-15; b) 30 grams tubes, NDC 52565-056-30; c) 80 grams tubes, NDC 52565-056-80, d) 1 lb (454 g) jars, NDC 52565-056-26; Rx Only, Teligent Pharma, Inc., Buena, New Jersey 08310.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0673-2022·2022-03-30
Clobetasol Propionate Ointment USP 0.05% Nationwide Recall
Teligent Pharma is recalling all unexpired batches of Clobetasol Propionate Ointment USP 0.05% nationwide because the manufacturer is discontinuing its stability study program, raising questions about product integrity.
Product
Clobetasol Propionate Ointment USP, 0.05%, packaged in a) 15 grams tube, NDC 52565-039-15; b) 30 grams tube, NDC 52565-039-30; c) 45 grams tube, NDC 52565-039-45; d) 60 grams tube, NDC 52565-039-60, Rx only, Manufactured by: Teligent Pharma, Inc., Buena, NJ 08310.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0694-2022·2022-03-30
Lidocaine Ointment USP 5% Recalled Due to cGMP Deviations
Teligent Pharma, Inc. is recalling all unexpired batches of Lidocaine Ointment USP, 5% nationwide and in Puerto Rico because the manufacturer is discontinuing its stability study program, a violation of good manufacturing practices.
Product
Lidocaine Ointment USP, 5%, Net Wt 35.44 g (1 1/4 oz) tube, Rx Only, Teligent Pharma, Inc., Buena, New Jersey 08310, NDC 52565-008-14.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0822-2022·2022-03-30
Medical device products from Family Dollar stores recalled for rodent contamination risk
Medical device products from Family Dollar stores in six Southern states are being recalled due to potential rodent activity at a distribution center. Affected items include feminine hygiene products, surgical masks, contact lens solutions, and bandages.
Product
Medical Device products purchased from Family Dollar retail stores located in Alabama, Arkansas, Louisiana, Mississippi, Missouri and Tennessee. The general categories of products, but are limited to these products, includes: feminine hygiene products, surgical masks, contact…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0824-2022·2022-03-30
Cytocell Microscope Slides Recall: Incorrect Expiry Date on Label
Cytocell Ltd. is recalling Cytocell 8 Square Template Slides because the outer label displays an incorrect expiration date of 2023-05 when the actual validated shelf life expires 2022-02.
Product
Cytocell 8 Square Template Slides (Glass)- microscope slides Reference: PCN008
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0682-2022·2022-03-30
Econazole Nitrate Cream Recalled Due to Manufacturing Process Deviations
Teligent Pharma is recalling Econazole Nitrate Cream, 1% due to current Good Manufacturing Practice deviations related to discontinued stability studies. Approximately 151,975 tubes distributed nationwide are affected.
Product
Econazole Nitrate Cream, 1%, packaged in a) 15 grams tubes, NDC 52565-022-15; b) 85 grams tubes, NDC 52565-022-85; c) 30 grams tubes, NDC 52565-022-30, Rx Only, Manufactured by: Teligent Pharma, Inc., Buena, New Jersey 08310.
Category
Drug
Distribution
Distributed nationwide