State

Louisiana product recalls

73,737 recalls have nationwide distribution and so reach Louisiana. 6,965 additional recalls listed Louisiana specifically in their distribution scope.

What the numbers show

Total: 6,965
Critical: 1,107
Severe: 1,739
Most recent: 2026-10-28

Of the 6,965 recalls naming Louisiana we have scored against our rubric, 1,107 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,739 (25%) are Severe.

Which agencies issued them

These figures cover only the 6,965 recalls whose distribution notice names Louisiana specifically. The 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

33726–33750 of 80702

SevereFDA (Drugs)·D-0547-2020·2019-12-11
QuVa Pharma Recalls Fentanyl and Bupivacaine Bags Due to Particulate Matter
QuVa Pharma is recalling specific lots of fentanyl and bupivacaine injection bags due to the presence of particulate matter, including potential glass particles.
Product
fentaNYL 500 mcg/250 mL (2 mcg/mL) 0.125% BUPivacaine HCl 312.5 mg/250 mL (1.25 mg/mL) in 0.9% Sodium Chloride 250 mL Bag, Rx, QuVA Pharma 1075 West Park One Drive, Suite 100 Sugar Land, TX 77478 NDC 70092-1105-37
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0541-2020·2019-12-11
Sanofi Recalls Zantac 150 mg Tablets Due to NDMA Impurity
Sanofi-Aventis U.S. LLC is recalling Regular Strength Zantac 150 mg tablets nationwide because an NDMA impurity was detected. This action addresses current good manufacturing practice (CGMP) deviations.
Product
Regular Strength Zantac 150 mg, Distributed by: Chattem, Inc., a Sanofi Company P.O. Box 2219, Chattanooga, TN 37409-0219. NDC 67751-151-01.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0554-2020·2019-12-11
QuVa Pharma Recalls Fentanyl and Ropivacaine Infusions Due to Particulate Matter
QuVa Pharma is recalling specific lots of fentanyl and ropivacaine infusions due to the potential presence of glass particulate matter.
Product
fentaNYL 400 mcg/200 mL (2 mcg/mL) ROPivacaine HCl 0.2% 400 mg/200 mL (2 mg/mL) in 0.9% Sodium Chloride 200 mL CADD Preservative Free, Rx, QuVA Pharma 1075 West Park One Drive, Suite 100 Sugar Land, TX 77478 NDC 70092-1440-76
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0544-2020·2019-12-11
Sanofi Recalls Zantac 150 mg Tablets Due to NDMA Impurity
Sanofi-Aventis U.S. LLC is recalling Zantac 150 mg tablets nationwide because an NDMA impurity was detected in the product.
Product
Zantac 150 mg, Distributed by: Chattem, Inc., a Sanofi Company P.O. Box 2219, Chattanooga, TN 37409-0219. NDC's 66715-9736-2 66715-9736-3 66715-9736-8
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0568-2020·2019-12-11
QuVa Pharma Recalls Fentanyl and Bupivacaine Infusion Due to Glass Particulates
QuVa Pharma is recalling specific lots of a fentanyl and bupivacaine infusion due to the presence of glass particulates.
Product
fentaNYL 800 mcg/200 mL (4 mcg/mL) BUPivacaine HCl 0.1667% 333.4 mg/200 mL (1.667 mg/mL) in 0.9% Sodium Chloride 200 mL in 250 mL CADD Preservative Free, Rx, QuVA Pharma 1075 West Park One Drive, Suite 100 Sugar Land, TX 77478 NDC 70092-1436-76
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0534-2020·2019-12-11
Sanofi Recalls Zantac Tablets Due to NDMA Impurity
Sanofi is recalling Cool Mint Tablets Maximum Strength Zantac 150 mg nationwide because NDMA impurity was detected in the product.
Product
Cool Mint Tablets Maximum Strength Zantac 150 mg Sanofi Distributed by: Chattem, Inc., a Sanofi Company P.O. Box 2219, Chattanooga, TN 37409-0219. NDC's: 0597-0120-06, 0597-0120-08, 0597-0120-09, 0597-0120-24, 0597-0120-38, 0597-0120-50, 0597-0120-76…
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0561-2020·2019-12-11
QuVa Pharma Recalls Fentanyl and Ropivacaine Bags Due to Glass Particulates
QuVa Pharma is recalling specific lots of fentanyl and ropivacaine injection bags due to the presence of glass particulates.
Product
fentaNYL 200 mcg/100 mL (2 mcg/mL) ROPivacaine HCl 0.2% 200 mg/100 mL (2 mg/mL) in 0.9% Sodium Chloride , 100 mL bag, Preservative Free, Rx, QuVA Pharma 1075 West Park One Drive, Suite 100 Sugar Land, TX 77478 NDC 70092-1108-36
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0545-2020·2019-12-11
Sanofi Recalls Zantac 75 mg Tablets Due to NDMA Impurity
Sanofi-Aventis U.S. LLC is recalling Zantac 75 mg tablets nationwide because NDMA impurity was detected. The recall covers all lots of the product.
Product
Zantac 75 mg, Distributed by: Chattem, Inc., a Sanofi Company P.O. Box 2219, Chattanooga, TN 37409-0219. NDC's 0597-0122-01 0597-0122-08 0597-0122-13 0597-0122-37 0597-0122-40 0597-0122-54 0597-0122-61 0597-0122-81 0597-0122-96
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0551-2020·2019-12-11
QuVa Pharma Recalls Fentanyl Syringes Due to Glass Particulate Matter
QuVa Pharma is recalling fentanyl syringes due to the potential presence of glass particulate matter. The recall is classified as FDA Class II.
Product
fentaNYL 1500 mcg/30 mL (50 mcg/mL) 30 mL in 35 mL Syringe Preservative Free, Rx, QuVA Pharma 1075 West Park One Drive, Suite 100 Sugar Land, TX 77478 NDC 70092-1099-49
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0567-2020·2019-12-11
QuVa Pharma Recalls Fentanyl Injection Bags Due to Glass Particulates
QuVa Pharma is recalling fentanyl injection bags due to the potential presence of glass particulates.
Product
fentaNYL 1250 mcg/250 mL (5 mcg/mL) in 0.9% Sodium Chloride 250 mL Bag Preservative Free, Rx, QuVA Pharma 1075 West Park One Drive, Suite 100 Sugar Land, TX 77478 NDC 70092-1444-05
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0543-2020·2019-12-11
Sanofi Recalls Zantac 75 mg Due to NDMA Impurity
Sanofi is recalling Regular Strength Zantac 75 mg tablets nationwide because an NDMA impurity was detected in the product.
Product
Regular Strength Zantac 75 mg, Distributed by: Chattem, Inc., a Sanofi Company P.O. Box 2219, Chattanooga, TN 37409-0219. NDC 68151-2584-0.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0556-2020·2019-12-11
QuVa Pharma Recalls Fentanyl Injection Due to Glass Particulate Matter
QuVa Pharma is recalling fentanyl 100 mcg/2 mL injections because of potential glass particulate matter. The recall covers specific lots distributed nationwide.
Product
fentaNYL 100 mcg/2 mL (50 mcg/mL) Preservative Free, Rx, QuVA Pharma 1075 West Park One Drive, Suite 100 Sugar Land, TX 77478 NDC 70092-1097-43
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0593-2020·2019-12-11
Stryker Recalls Disposable Tourniquet Cuffs Due to Air Leak Risk
Stryker is recalling 16,380 disposable tourniquet cuffs because they may leak air, causing a loss of vascular occlusion during surgery.
Product
Color Cuff Disposable Tourniquet Cuff, 18 inch X 3 inch, 1BLA (Single Bladder), 2PRT(Dual Port) Quick Connect Connector, Product Number 5921-018-235 - Product Usage: The Stryker Disposable Tourniquet Cuff (cuff) is indicated for use in surgical procedures that require the…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0210-2020·2019-12-11
Frog Hollow Holiday Fruitcake Recalled for Missing Walnut Ingredient Labeling
Frog Hollow Farm is recalling 60 Holiday Fruitcakes because walnuts were not listed on the ingredient label, posing an allergen risk.
Product
Frog Hollow Holiday Fruitcake Incorrect ingredients: Organic butter, organic flour, organic sugar, organic eggs, molasses, candied orange peel, rum, dried plums, organic dried peaches. Correct label: organic butter, organic flour, organic sugar, organic eggs, organic…
Category
Food
Distribution
22 states
HighFDA (Drugs)·D-0550-2020·2019-12-11
QuVa Pharma Recalls Fentanyl and Bupivacaine Injection Due to Particulate Matter
QuVa Pharma is recalling fentanyl and bupivacaine injection bags due to the presence of particulate matter, specifically potential glass particles.
Product
fentaNYL 200 mcg/100 mL (2 mcg/mL) BUPivacaine HCl 0.125% 125 mg/100 mL (1.25 mg/mL) in 0.9% Sodium Chloride Preservative Free, 100 mL in 150 Bag, Rx, QuVA Pharma 1075 West Park One Drive, Suite 100 Sugar Land, TX 77478 NDC 70092-1104-36
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0586-2020·2019-12-11
Steris Evolution Loading Car and Transfer Carriage Recall for Locking Pin Defect
Steris Corporation is recalling 237 Evolution Loading Cars and Transfer Carriages because a locking pin defect may cause the equipment to fall forward unexpectedly.
Product
Evolution Loading Car and Transfer Carriage- Accessory to the Sterilizer, Steam
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0602-2020·2019-12-11
CooperSurgical Recalls Quantum 2000 Electrosurgical Generators Due to Malfunction
CooperSurgical is recalling Quantum 2000 Electrosurgical Generators because they may stop cutting, coagulating, or blending during procedures when the foot pedal is used.
Product
Quantam 2000 Electrosurgical Generator, Part number 909075-05W.
Category
Medical Device
Distribution
28 states
HighFDA (Devices)·Z-0604-2020·2019-12-11
Steris Eagle 3000 Sterilizer Recall Due to Incorrect Safety Valve
Steris is recalling 236 Eagle 3000 Small Steam Sterilizers because the preventive maintenance kit may contain an incorrect pressure safety valve.
Product
Eagle 3000 Sterilizer, small steam sterilizer. Product Usage: The Eagle 3000 Small Sterilizer is designed for sterilization of certain materials used in healthcare facilities, and are available in two configurations: Gravity designed for sterilization of non-porous, heat- and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0560-2020·2019-12-11
QuVa Pharma Recalls Fentanyl Syringes Due to Glass Particulate Matter
QuVa Pharma is recalling fentanyl 250 mcg/5 mL syringes due to the presence of glass particulate matter. The recall is nationwide.
Product
fentaNYL 250 mcg/5 mL (50 mcg/mL), 5 mL Syringe, Preservative Free, Rx, QuVA Pharma 1075 West Park One Drive, Suite 100 Sugar Land, TX 77478 NDC 70092-1098-44
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0548-2020·2019-12-11
QuVa Pharma Recalls Fentanyl and Ropivacaine Infusions Due to Particulate Matter
QuVa Pharma is recalling specific lots of fentanyl and ropivacaine infusions due to the presence of particulate matter, including potential glass particles.
Product
fentaNYL 200 mcg/100 mL (2 mcg/mL) ROPivacaine HCl 0.2% 200 mg/100 mL (2 mg/mL) in 0.9% Sodium Chloride 100 mL CADD, Rx, QuVA Pharma 1075 West Park One Drive, Suite 100 Sugar Land, TX 77478NDC 70092-1259-75
Category
Drug
Distribution
Distributed nationwide
HighCPSC·20039·2019-12-11
Profile Design Recalls Carbon Aerobars Due to Crash Hazard
Profile Design is recalling Aeria Ultimate carbon aerobars because they can crack and break, causing riders to lose control and crash.
Product
Aeria Ultimate carbon aerobars
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0557-2020·2019-12-11
QuVa Pharma Recalls Fentanyl and Bupivacaine Injection Due to Particulate Matter
QuVa Pharma is recalling fentanyl and bupivacaine injection products due to the presence of particulate matter, specifically potential glass particles.
Product
fentaNYL 200 mcg/100 mL (2 mcg/mL) 0.125% Bupivacaine HCl 125 mg/100 mL (1.25 mg/mL) in 0.9% Sodium Chloride, 100 mL CADD Preservative Free, Rx, QuVA Pharma 1075 West Park One Drive, Suite 100 Sugar Land, TX 77478 NDC 70092-1202-75
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·19V882000·2019-12-11
Indian Recalls 2019 Motorcycles Due to Defective Circuit Breaker
Indian Motorcycle is recalling 5,474 2019 models because a defective circuit breaker may cause sudden engine stalls, increasing crash risk.
Product
INDIAN — INDIAN CHIEFTAIN, ROADMASTER, SPRINGFIELD, SPRINGFIELD DARK HORSE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0533-2020·2019-12-11
Fagron Recalls LETS GEL Kits Due to Microbial Contamination
Fagron, Inc. is recalling 11,912 kits of LETS GEL Convenience Packs due to microbial contamination of the non-sterile product.
Product
LETS GEL KIT Convenience Pack (To prepare 100 mL LETS GEL), Contains: LETS Powders for Gel: Lidocaine Hydrochloride - 4 g, Ephinephrine Bitartrate - 180 mg, Tetracaine Hydrochloride - 500 mg, Sodium Metabisulfite - 75 mg, SuturaGel Methlcellulose Base; RX Only, For Prescription…
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0600-2020·2019-12-11
CooperSurgical Recalls Quantum 2000 Electrosurgical Generators Due to Malfunction
CooperSurgical is recalling 105 Quantum 2000 Electrosurgical Generators because they may stop cutting, coagulating, or blending during procedures.
Product
Quantam 2000 Electrosurgical Generator, Part number 909075.
Category
Medical Device
Distribution
28 states