State

Louisiana product recalls

73,817 recalls have nationwide distribution and so reach Louisiana. 6,966 additional recalls listed Louisiana specifically in their distribution scope.

What the numbers show

Total: 6,966
Critical: 1,107
Severe: 1,740
Most recent: 2026-11-04

Of the 6,966 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 1,740 (25%) are Severe.

Which agencies issued them

These figures cover only the 6,966 recalls whose distribution notice names Louisiana specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

46451–46475 of 80783

SevereFDA (Drugs)·D-0960-2017·2017-07-19
Teva Recalls Paliperidone Extended-Release Tablets Due to Dissolution Failure
Teva Pharmaceuticals is recalling 360 bottles of Paliperidone Extended-Release Tablets because one tablet failed a routine stability test for drug release.
Product
Paliperidone Extended-Release Tablets, 3 mg, 90 count bottles, Rx only, Manufactured by: Actavis Laboratories FL, Inc., Fort Lauderdale, FL 33314 USA Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054, USA, NDC: 0591-3693-19
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0972-2017·2017-07-19
Baxter Recalls 5% Dextrose Injection Due to Sterility Concerns
Baxter Healthcare is recalling 54,528 bags of 5% Dextrose Injection because the bags may leak, compromising sterility.
Product
DEXTROSE — DEXTROSE (DEXTROSE MONOHYDRATE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0959-2017·2017-07-19
Bristol-Myers Squibb Recalls Eliquis 5mg Tablets Due to Labeling Error
Bristol-Myers Squibb is recalling 48,180 bottles of Eliquis 5mg tablets because one bottle was found to contain 2.5mg tablets instead.
Product
EliquisTablets 5mg, 60 count bottle, Rx Only, Marketed by: Bristol-Meyers Squibb Company Princeton, NJ 08543 USA and Pfizer Inc. New York, NY 10017 USA, NDC 0003-0894-21
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·17V450000·2017-07-19
Daimler Trucks Recalls 2017-2018 Freightliner and Western Star Trucks for Fuel Pump Defect
Daimler Trucks is recalling specific 2017-2018 Freightliner and Western Star trucks because a fuel pump drive gear may slip, causing sudden engine stalls and increasing crash risk.
Product
FREIGHTLINER CUSTOM CHASS — FREIGHTLINER CUSTOM CHASS, FREIGHTLINER, WESTERN STAR XCP, 122SD, 6900, XCM
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0979-2017·2017-07-19
SCA Pharmaceuticals Recalls Potassium Phosphate IV Bags Due to Sterility Concerns
SCA Pharmaceuticals is recalling 20 bags of Potassium Phosphate IV solution due to a lack of sterility assurance. The affected product was distributed in LA, PA, NY, and WI.
Product
Potassium PHOSphate added to 0.9% Sodium Chloride 250 mL Bag 30 mMol (44 mEq K+) Total Approximate Volume 260 mL, Rx only, SCA Pharmaceuticals, Little Rock, AR 72205, NDC 70004-0843-40
Category
Drug
Distribution
4 states
SevereFDA (Drugs)·D-0978-2017·2017-07-19
SCA Pharmaceuticals Recalls Potassium Phosphate IV Bags Due to Sterility Concerns
SCA Pharmaceuticals is recalling 20 bags of Potassium Phosphate IV solution due to a lack of sterility assurance. The affected product was distributed in LA, PA, NY, and WI.
Product
Potassium PHOSphate added to 250 mL 0.9% Sodium Chloride 15 mMol (22 mEq K+) Total Approximate Volume 255 mL, Rx only, SCA Pharmaceuticals, Little Rock, AR 72205, NDC 70004-0841-32
Category
Drug
Distribution
4 states
SevereFDA (Drugs)·D-0976-2017·2017-07-19
SCA Pharmaceuticals Recalls Potassium Phosphate IV Bags Due to Sterility Concerns
SCA Pharmaceuticals is recalling 221 bags of Potassium Phosphate IV solution due to a lack of sterility assurance. The product was distributed in LA, PA, NY, and WI.
Product
Potassium PHOSphate added to 250 mL 0.9% Sodium Chloride 10 mMol (14.67 mEq K+) Total Approximate Volume 254 mL, Rx only, SCA Pharmaceuticals, Little Rock, AR 72205, NDC 70004-0840-40
Category
Drug
Distribution
4 states
SevereFDA (Drugs)·D-0953-2017·2017-07-19
Advanced Pharma Recalls Succinylcholine Chloride Injection Due to Sterility Concerns
Advanced Pharma Inc. is recalling QUELICIN (Succinylcholine Chloride) Injection due to a lack of assurance of sterility. The recall affects 2,350 units distributed nationwide.
Product
QUELICIN (Succinylcholine Chloride) Injection, USP 20 mg/mL in a) 5 mL vial (NDC 15082-814-67), b) 7mL vial (NDC 15082-814-79), c) 10mL vial (NDC 15082-814-61), Repackaged by Advanced Pharm, 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0954-2017·2017-07-19
Advanced Pharma Recalls Potassium Phosphate IV Bags Due to Sterility Concerns
Advanced Pharma Inc. is recalling 72 units of Potassium Phosphate IV bags nationwide due to a lack of assurance of sterility.
Product
Potassium Phosphate (USP) QS 0.9% Sodium Chloride (USP) 250 mL 20 mmol in NS 250mL Bag, Advanced Pharma, 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404. NDC15082-926-25
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0955-2017·2017-07-19
Advanced Pharma Recalls Potassium Phosphate Bags Due to Sterility Concerns
Advanced Pharma Inc. is recalling specific lots of Potassium Phosphate in 0.9% Sodium Chloride bags because the company cannot assure the product's sterility.
Product
Potassium Phosphate (USP) QS 0.9% Sodium Chloride (USP) 250 mL 30 mmol in NS 250mL Bag, Advanced Pharma, 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404. NDC15082-924-25
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2705-2017·2017-07-19
O-Two Adult Ventilation Timer Recalled Due to Flash Rate Malfunction
O-Two Medical Technologies is recalling Adult Ventilation Timers because the flash rate may be twice the labeled rate, potentially affecting ventilation guidance.
Product
O-Two Adult Ventilation Timer, MODEL #(s): 01BM1000-CS, 01BM3201-MOTP-CS, 01BM3201-MOTL-CS, CATALOG #(s): 01BM1000 --- INTENDED USE: The Adult Ventilation Timer is intended to guide the rescuer to provide ventilations at a rate appropriate for adult patients
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2729-2017·2017-07-19
Natus Neurology Recalls Elite 5 MHz Vascular Probes Due to Noise Issues
Natus Neurology is recalling 2,335 Elite 5 MHz Vascular Probes because excessive background noise may mask heart rate and blood flow signals.
Product
Nicolet¿ Elite¿ 5 MHz Vascular Probe, Model #: X1L004, Catalog Code: N500. Intended for non-invasive support, i.e. early detection of fetal life, monitor blood flow before and after surgery, etc.
Category
Medical Device
Distribution
44 states
HighFDA (Devices)·Z-2695-2017·2017-07-19
St. Jude Medical Recalls Infinity 7 Implantable Pulse Generators
St. Jude Medical is recalling 373 Infinity 7 Implantable Pulse Generators because exposure to monopolar electrosurgical devices may cause a loss of neuromodulation therapy.
Product
Infinity 7, Implantable Pulse Generator, REF 6662, Rx only, STERILE EO Product Usage: The Infinity IPG is an electronic device designed to be connected to one or two extensions. It is powered by a hermetically sealed battery within a titanium case and uses microelectronic…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2679-2017·2017-07-19
ICU Plum A+ Infusion Systems Recalled for Battery-Related Therapy Interruption
ICU is recalling Plum A+ Infusion Systems because battery issues can cause an E321 error code, potentially interrupting therapy.
Product
The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self contained, microprocessor based infusion devices. The pumps are…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2694-2017·2017-07-19
St. Jude Medical Recalls Infinity 5 Implantable Pulse Generators
St. Jude Medical is recalling 54 Infinity 5 Implantable Pulse Generators due to a risk of therapy loss if exposed to monopolar electrosurgical devices.
Product
Infinity 5, Implantable Pulse Generator, REF 6661, Rx only, STERILE EO Product Usage: The Infinity IPG is an electronic device designed to be connected to one or two extensions. It is powered by a hermetically sealed battery within a titanium case and uses microelectronic…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2731-2017·2017-07-19
O-Two Medical Recalls Burn Relief Dressings Due to Sterilization Concerns
O-Two Medical Technologies is voluntarily recalling specific lots of Burn Relief hydrogel dressings because there is a lack of evidence validating the sterilization dose, posing a potential contamination risk.
Product
Burn Relief¿, MODEL #(s): 06BK1221, 06BK1232, 06BK1201, 06BK1200, CATALOG #(s): 06BK1221, 06BK1232, 06BK1201, 06BK1200 --- DRESSING,WOUND,HYDROGEL W/OUT DRUG AND/OR BIOLOGIC. --- Burn Relief¿ products are self-cooling, non-adhering and are intended to be used on 1st and 2nd…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2696-2017·2017-07-19
St. Jude Medical Recalls Infinity 7 Implantable Pulse Generators
St. Jude Medical is recalling 40 Infinity 7 Implantable Pulse Generators because exposure to monopolar electrosurgical devices during medical procedures may cause a loss of neuromodulation therapy.
Product
Infinity 7, Implantable Pulse Generator, REF 6663, Rx only, STERILE EO Product Usage: The Infinity IPG is an electronic device designed to be connected to one or two extensions. It is powered by a hermetically sealed battery within a titanium case and uses microelectronic…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0973-2017·2017-07-19
Baxter Recalls Sodium Chloride Injection Bags Due to Sterility Concerns
Baxter Healthcare is recalling 295,200 bags of 0.9% Sodium Chloride Injection due to a lack of assurance of sterility and potential for leaking.
Product
SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2677-2017·2017-07-19
ICU Recalls 71 Plum A+ Infusion Systems Due to Battery Error
ICU is recalling 71 Plum A+ Infusion Systems because a battery issue can trigger an E321 error code, potentially interrupting therapy.
Product
The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self contained, microprocessor based infusion devices. The pumps are…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2681-2017·2017-07-19
ICU Plum A+ Infusion Systems Recalled for Battery-Related Therapy Interruption
ICU is recalling 21,703 Plum A+ Infusion Systems because battery issues can cause an E321 error code, potentially interrupting therapy.
Product
The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self contained, microprocessor based infusion devices. The pumps are…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2676-2017·2017-07-19
ICU Recalls Plum A+ Infusion Systems Due to Battery-Related Therapy Interruption
ICU is recalling 10,609 Plum A+ Infusion Systems because a battery issue can trigger an E321 error code, potentially interrupting patient therapy.
Product
The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self contained, microprocessor based infusion devices. The pumps are…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2703-2017·2017-07-19
GE Healthcare Recalls Carestation Monitors for Potential Malfunction
GE Healthcare is recalling Carestation 620, 650, and 650c monitors due to potential for elevated FiCO2 readings and unexpected system malfunctions.
Product
Carestation 620 A1, Carestation 650 A1, and Carestation 650c A1
Category
Medical Device
Distribution
35 states
HighFDA (Devices)·Z-2675-2017·2017-07-19
ICU Recalls 180 Plum A+ Infusion Systems Due to Battery Issues
ICU is recalling 180 Plum A+ Infusion Systems because battery issues may cause an E321 error code and interrupt therapy.
Product
The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self contained, microprocessor based infusion devices. The pumps are…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2709-2017·2017-07-19
Toshiba XARIO 200 Ultrasound System Recalled for Incorrect Velocity Trace Values
Toshiba American Medical Systems is recalling XARIO 200 diagnostic ultrasound systems because the Continuous Trace method may display incorrect velocity trace values.
Product
XARIO 200 TUS-X200 diagnostic ultrasound system
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2713-2017·2017-07-19
Pentax Video Duodenoscope Recall for Surface Soiling Investigation
Pentax of America Inc. issued a field correction for two Video Duodenoscope models to investigate surface soiling on the suction cylinder and distal cap.
Product
Video Duodenoscope These instruments are intended to provide optical visualization of (via a video monitor), and therapeutic access to, the biliary tract via the upper GI tract. This anatomy includes, but is not restricted to, the organs; tissues; and subsystems: esophagus…
Category
Medical Device
Distribution
Distributed nationwide