State

Tennessee product recalls

73,833 recalls have nationwide distribution and so reach Tennessee. 7,861 additional recalls listed Tennessee specifically in their distribution scope.

What the numbers show

Total: 7,861
Critical: 1,324
Severe: 1,974
Most recent: 2026-11-14

Of the 7,861 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 7,861 recalls whose distribution notice names Tennessee specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

53101–53125 of 81694

SevereFDA (Drugs)·D-1308-2016·2016-07-20
Pharmakon Recalls Fentanyl and Bupivacaine Compounded Syringes for Sterility Concerns
Pharmakon Pharmaceuticals is recalling 260 syringes of compounded fentanyl and bupivacaine due to a lack of assurance of sterility.
Product
Fentanyl Citrate 2.5 mcg/mL & Bupivacaine 0.075% in 0.9% Sodium Chloride, 60 mL BD syringe, Rx Only, Compounded by PHARMAKON Pharmaceuticals, Noblesville, IN 46060, NDC # 45183-0826-77
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1319-2016·2016-07-20
Pharmakon Recalls Fentanyl and Bupivacaine Bags Due to Sterility Concerns
Pharmakon Pharmaceuticals is recalling 870 bags of compounded Fentanyl and Bupivacaine due to a lack of assurance of sterility.
Product
Fentanyl Citrate 2 mcg/mL & Bupivacaine HCL 0.125 % in 0.9% Sodium Chloride, 150 mL lntravia bag;, Rx Only, Compounded by PHARMAKON Pharmaceuticals, Noblesville, IN 46060, NDC 45183-0905-48
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1273-2016·2016-07-20
Pharmakon Recalls Promethazine Injection Due to Sterility Concerns
Pharmakon Pharmaceuticals is recalling 40 units of compounded Promethazine injection due to a lack of assurance of sterility. The product was distributed nationwide to VA and DOD facilities.
Product
Promethazine 6.25 mg added to 0.9% Sodium Chloride 50 mL in 100 mL B/Braun PAB bag, Rx Only, Compounded by PHARMAKON Pharmaceuticals, Noblesville, IN 46060, NDC 45183-0177-41
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1294-2016·2016-07-20
Pharmakon Recalls Ketamine Syringes Due to Sterility Assurance Concerns
Pharmakon Pharmaceuticals is recalling 600 vials of compounded Ketamine 100mg/mL due to a lack of assurance of sterility. The product was distributed nationwide to VA and DOD facilities.
Product
Ketamine 100mg/mL 1mL fill 3 mL syringe, Rx Only, Compounded by PHARMAKON Pharmaceuticals, Noblesville, IN 46060, NDC 45183-0709-78
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1176-2016·2016-07-20
Medaus Recalls Calcium Sodium EDTA Vials Due to Sterility Concerns
Medaus, Inc. is recalling specific lots of Calcium Sodium EDTA 300mg/mL vials because the agency cannot assure the product's sterility.
Product
CALCIUM SODIUM EDTA 300MG/ML (PF), 10ML Vials, MEDAUS PHARMACY
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1256-2016·2016-07-20
Pharmakon Recalls Phenylephrine Injection Due to Sterility Concerns
Pharmakon Pharmaceuticals is recalling Phenylephrine 40 mcg/mL injection syringes due to a lack of assurance of sterility.
Product
Phenylephrine 40 mcg/mL injection in 0.9% Sodium Chloride 10 mL syringe, Rx Only, Compounded by PHARMAKON Pharmaceuticals, Noblesville, IN 46060, NDC 45183-0011-72
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1191-2016·2016-07-20
Medaus Recalls Hydroxy B12 Vials Due to Sterility Assurance Concerns
Medaus, Inc. is recalling Hydroxy B12 5mg/mL vials because the company cannot ensure the product is sterile.
Product
HYDROXY B12 5MG/ML IN NACL 0.9% (PF), In a) 1ML Vials and b) 2ML Vials, MEDAUS PHARMACY
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1332-2016·2016-07-20
Pharmakon Recalls Lidocaine Syringes Due to Sterility Assurance Concerns
Pharmakon Pharmaceuticals is recalling 50 vials of Lidocaine 2% syringes because the company cannot ensure the products are sterile.
Product
Lidocaine 2%, 5 mL syringe, Rx Only, Compounded by PHARMAKON Pharmaceuticals, Noblesville, IN 46060, NDC 45183-0946-70
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1254-2016·2016-07-20
Medaus Recalls Hydrochloric Acid Vials Due to Sterility Concerns
Medaus, Inc. is recalling specific lots of HCL 2MG/ML (PF) 5ML Vials because the company cannot ensure the product is sterile.
Product
HCL 2MG/ML (PF), 5ML Vials, MEDAUS PHARMACY
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1309-2016·2016-07-20
Pharmakon Recalls Diltiazem HCI Bags Due to Sterility Concerns
Pharmakon Pharmaceuticals is recalling 10 bags of Diltiazem HCI 250 mg in 5% Dextrose due to a lack of assurance of sterility.
Product
Diltiazem HCI 250 mg in 5% Dextrose, 250 mL lntravia bag, Rx Only, Compounded by PHARMAKON Pharmaceuticals, Noblesville, IN 46060, NDC 45183-0853-02
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1267-2016·2016-07-20
Pharmakon Recalls Midazolam Syringes Due to Sterility Assurance Concerns
Pharmakon Pharmaceuticals is recalling 40 vials of compounded Midazolam (PF) 5mg/ml 25 mL BD syringes due to a lack of assurance of sterility.
Product
Midazolam (PF) 5mg/ml 25 mL BD syringe, Rx Only, Compounded by PHARMAKON Pharmaceuticals, Noblesville, IN 46060, NDC # 45183-0138-67
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1171-2016·2016-07-20
Medaus Recalls B-Complex Vials Due to Sterility Concerns
Medaus, Inc. is recalling B-Complex Without B12 vials because the FDA could not ensure the product was sterile. The recall covers 5 mL and 10 mL vials distributed in the U.S., Japan, and New Zealand.
Product
B-COMPLEX WITHOUT B12 W/PRES (BENZYL ETOH 2%), B1-100MG, B2-5-PO4-2MG, B3-50MG, B5-2MG, B6-2MG/ML, In a) 5ML Vials and b) 10ML Vials, MEDAUS PHARMACY
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1195-2106·2016-07-20
Medaus Recalls L-Carnitine Vials Due to Sterility Concerns
Medaus, Inc. is recalling L-Carnitine 50mg/mL vials because the company cannot ensure the product is sterile. The recall covers distribution in the U.S., Japan, and New Zealand.
Product
L-CARNITINE 50MG/ML (PF), 10ML Vials, MEDAUS PHARMACY
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1210-2016·2016-07-20
Medaus Recalls Lipo-Injection Vials Due to Sterility Concerns
Medaus, Inc. is recalling Lipo-Injection vials because the company cannot ensure the product is sterile. The recall covers 5 mL and 10 mL vials distributed in the U.S., Japan, and New Zealand.
Product
LIPO-INJECTION W/LIDOCAINE W/PRES. (BENZYL ETOH 2%) ASCORBIC ACID-50MG, B1-50MG, B2-5 PO4-5MG, B-3-50MG, B5-5MG, B6-5MG, CYANO B12-100MCG, METHIONINE 12.5MG, INOSITOL 25MG, CHOLINE CHL-25MG, LIDOCAINE-10MG/ML, In a) 5ML Vials and b) 10ML Vials, MEDAUS PHARMACY
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-1644-2016·2016-07-20
Dr. Praeger's Recalls Frozen Veggie Balls Due to Listeria Risk
Dr. Praeger's Sensible Foods is voluntarily recalling frozen California Veggie Balls because they may be contaminated with Listeria monocytogenes.
Product
Dr. Praeger's California Veggie Balls (Vegan), 1 oz., 10 lbs. (4.54 kg), Best if used by: May-12-2018, UPC (01) 0 0080868 01310, Dr. Praeger's Sensible Foods, Elmwood Park, NJ 07407
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1634-2016·2016-07-20
Dr. Praeger's Recalls Frozen Kale Burgers Due to Listeria Risk
Dr. Praeger's Sensible Foods is voluntarily recalling Aldi Kale Burgers because they may be contaminated with Listeria monocytogenes.
Product
Aldi Kale Burger, Net 18.75 lbs, 30 x 10 oz (284 grams), Sell By: May -17-2018
Category
Food
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1318-2016·2016-07-20
Pharmakon Recalls Vancomycin HCL 1.25 GM Bags Due to Sterility Concerns
Pharmakon Pharmaceuticals is recalling 216 units of Vancomycin HCL 1.25 GM in 5% Dextrose bags due to a lack of assurance of sterility.
Product
Vancomycin HCL 1.25 GM added to 5% Dextrose in a 250 mL lntravia bag, Rx Only, Compounded by PHARMAKON Pharmaceuticals, Noblesville, IN 46060, NDC 45183-0885-02
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1265-2016·2016-07-20
Pharmakon Recalls Epinephrine Injection Due to Sterility Concerns
Pharmakon Pharmaceuticals is recalling 280 vials of compounded Epinephrine injection due to a lack of assurance of sterility. The product was distributed nationwide and to specific VA/DOD facilities.
Product
Epinephrine 100mcg/mL injection in 0.9% Sodium Chloride 10 mL BD syringe, Rx Only, Compounded by PHARMAKON Pharmaceuticals, Noblesville, IN 46060, NDC 45183-0120-72
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1303-2016·2016-07-20
Pharmakon Recalls Norepinephrine Bags Due to Sterility Concerns
Pharmakon Pharmaceuticals is recalling 70 bags of Norepinephrine Bitartrate 8mg in 5% Dextrose due to a lack of assurance of sterility.
Product
Norepinephrine Bitartrate 8mg Added to 5% Dextrose 250 mL bag, Rx Only, Compounded by PHARMAKON Pharmaceuticals, Noblesville, IN 46060, NDC 45183-0806-02
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1322-2016·2016-07-20
Pharmakon Recalls Succinylcholine Chloride Syringes Due to Sterility Concerns
Pharmakon Pharmaceuticals is recalling 2,175 units of Succinylcholine Chloride 20 mg/mL syringes due to a lack of assurance of sterility.
Product
Succinylcholine Chloride 20 mg/mL, 10 mL BD syringe, Rx Only, Compounded by PHARMAKON Pharmaceuticals, Noblesville, IN 46060, NDC 45183-0920-72
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1298-2016·2016-07-20
Pharmakon Recalls Oxytocin Infusion Bags Due to Sterility Concerns
Pharmakon Pharmaceuticals is recalling 468 units of compounded Oxytocin 30 Units in Lactated Ringers due to a lack of assurance of sterility.
Product
Oxytocin 30 Units added to Lactated Ringers in a 500 mL lntravia bag, Rx Only, Compounded by PHARMAKON Pharmaceuticals, Noblesville, IN 46060, NDC 45183-0766-03
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1245-2016·2016-07-20
Medaus Recalls Testosterone Cypionate Vials Due to Sterility Concerns
Medaus, Inc. is recalling Testosterone Cypionate vials because the company cannot ensure the product is sterile. The recall covers vials distributed in the U.S., Japan, and New Zealand.
Product
TESTOSTERONE CYP 50 MG/ML W/PRES (BENZYL ETOH 2%), In a) 1ML Vials, b) 2ML Vials, c) 3ML Vials, d) 4ML Vials, and e) 5ML Vials, MEDAUS PHARMACY
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1237-2016·2016-07-20
Medaus Recalls Riboflamin Vials Due to Sterility Assurance Concerns
Medaus, Inc. is recalling specific lots of Riboflavin 10mg/mL vials because the company cannot ensure the product is sterile.
Product
RIBOFLAVIN 10MG/ML (PF), In a) 1ML Vials and b) 2ML Vials, MEDAUS PHARMACY
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1244-2016·2016-07-20
Medaus Recalls Testosterone Cypionate Vials Due to Sterility Concerns
Medaus, Inc. is recalling specific vials of Testosterone Cypionate 25 mg/mL due to a lack of assurance of sterility. The affected product was distributed in the U.S., Japan, and New Zealand.
Product
TESTOSTERONE CYP 25 MG/ML W/PRES (BENZYL ETOH 2%), 5ML Vials, MEDAUS PHARMACY
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1320-2016·2016-07-20
Pharmakon Recalls Fentanyl and Ropivacaine Bags Due to Sterility Concerns
Pharmakon Pharmaceuticals is recalling 20 bags of compounded Fentanyl Citrate and Ropivacaine HCI due to a lack of assurance of sterility.
Product
Fentanyl Citrate 2mcg/mL & Ropivacaine HCI 0.2% in 0.9% Sodium Chloride, 100 mL bag, Compounded by PHARMAKON Pharmaceuticals, Noblesville, IN 46060, NDC 5183-0906-48
Category
Drug
Distribution
Distributed nationwide