Recalls in Texas (page 40)
4158 recalls.
- Halls Cough Drops a) BAGS recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - TYLENOL a) 500 MG. recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - PEPCID COMPLETE - 25CT recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - PEPTO BISMOL 32CT recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - CHILDREN NYQUIL recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - NYQUIL COLD & FLU -32CT/2PK recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - LIQUID NYQUIL a) regular recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - MOTRIN 2'S DISP.- 50CT recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - EXCEDRIN MIGRAINE 2'S- 25 CT recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - EXCEDRIN 2'S DISP.- 30 CT recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - LIQUID DAYQUIL 12/8oz recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - DAYQUIL COLD & FLU recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - Claritin recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - Bayer 2Pk- 25 CT recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - Benadryl recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - Alka Seltzer recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - Aleve 1's recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - Advil a) Ibuprofen recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - AQ 120 GFEW recall (Encon Safety Products Co)
DrugClass IIReported January 21, 2026 · cGMP deviations. - Levothyroxine Sodium Tablets recall (Alvogen, Inc)
DrugClass IIReported January 21, 2026 · Product Mix-Up: A single bottle of this lot was reported by a pharmacy to contain 88 mcg tablets instead of 150 mcg tablets. - Clindamycin Phosphate USP recall (SUN PHARMACEUTICAL INDUSTRIES INC)
DrugClass IIIReported January 21, 2026 · Failed Impurities/Degradation: Out of Specification results for Total Impurities and for Assay. - Fluocinolone Acetonide Solution Topical Solution USP recall (SUN PHARMACEUTICAL INDUSTRIES INC)
DrugClass IIIReported January 21, 2026 · Failed Impurities/Degradation Specifications: Out of specification result was obtained for the known impurity D. - Abre Venous Self-Expanding Stent System recall (Medtronic Inc)
Medical deviceClass IIReported January 21, 2026 · Stents may be impacted by a Nitinol anomaly which causes a reduced stent diameter when deployed and corresponding reduced radial force. Issue may result in... - Plum Duo Infusion System recall (ICU Medical, Inc.)
Medical deviceClass IIReported January 21, 2026 · ICU Medical received one lot of defective primary speakers from our supplier that may fail to produce an audible sound. If the primary speaker in your Plum Duo... - ThinPrep¿ CytoLyt¿ Solution. Buffered Cell Wash Solution. recall (Hologic, Inc)
Medical deviceClass IIReported January 21, 2026 · Fungal contamination of affected lot with Parengyodontium album. - Philips Azurion Systems with software versions R2.1.10 and R2.2.10. Includes the... recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Six (6) identified software issues which may result in the following: system keeps restarting, AMC triple drive, C-Partition of Suite PC running out of free... - Medline medical procedure convenience kits labeled as: KIT ROBOTICS UROLOGY PROSTATE recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a change in design in 2024, irrigation solution is able to travel to the handpiece and... - Medline medical procedure convenience kits labeled as: 1) LAVH PROCEDURE recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a change in design in 2024, irrigation solution is able to travel to the handpiece and... - Medline medical procedure convenience kits labeled as: 1) ROBOTIC recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a change in design in 2024, irrigation solution is able to travel to the handpiece and... - Medline medical procedure convenience kits labeled as: 1) WCH BARI-GASTRECTOMY CDS recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a change in design in 2024, irrigation solution is able to travel to the handpiece and... - Medline medical procedure convenience kits labeled as: 1) LAPAROSCOPY CDS-LF recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a change in design in 2024, irrigation solution is able to travel to the handpiece and... - Medline medical procedure convenience kits labeled as: 1) THORACIC ROBOTICS recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a change in design in 2024, irrigation solution is able to travel to the handpiece and... - Asserachrom HPIA. Model/Catalog Number: 00615. The Asserachrom HPIA kit is... recall (Diagnostica Stago, Inc.)
Medical deviceClass IIReported January 21, 2026 · Potential for defect for Asserachrom HPIA lot 271288, which can affect every well in the impacted strip and produce negative results. - Philips Azurion Systems R3.0. Includes the following label descriptions and... recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Nine (9) identified software issues which may result in the following: loss of X-ray after Pedal Tap, loss of X-ray after Phase Fault, missing live X-ray on... - Allura Xper FD20/20 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD20/10 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD20 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD10/10 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD10 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD20 OR Table recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD20 Biplane recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD20 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD10/10 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD10 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD20 Biplane recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD20 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD10/10 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD10 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD10F recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Product Name: Allura Xper FD10C recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - BD Ready-to-Use Hydrophilic Catheter 14 Fr recall (HANGZHOU BEVER MEDICAL DEVICES CO., LTD.)
Medical deviceClass IIReported January 21, 2026 · Labeling error, Incorrect expiration date - Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check... - Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check... - Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check... - Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check... - Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check... - Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check... - Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check... - Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check... - Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check... - Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check... - Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check... - Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check... - A71200 Vanta" Clinician Programmer Application recall (Medtronic Neuromodulation)
Medical deviceClass IIReported January 21, 2026 · Complaints received that Vanta A71200 CP App does not function as intended during use. There is a potential for prolonged or postponed surgical procedure. - Curtis International Expands Recall of Frigidaire-brand Minifridges Due to Fire and Burn Hazards
Consumer productReported January 16, 2026 · The minifridges' internal electrical components can short circuit and ignite the surrounding plastic housing, posing fire and burn hazards. - RootStim Recalls Beard Growth Serum Spray Bottles Due to Risk of Serious Injury or Death from Child Poisoning; Violate Mandatory Standard for Child-Resistant Packaging
Consumer productReported January 16, 2026 · The beard growth serum contains minoxidil, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The serum's... - Greatale Recalls Self-Feeding Pillows Due to Risk of Serious Injury or Death from Aspiration and Suffocation
Consumer productReported January 16, 2026 · The recalled self-feeding pillows hold the bottle at an unsafe angle while keeping it fixed in place so the infant cannot pull away. This can lead to... - HEZI Brand Power Strips Recalled Due to Risk of Serious Injury or Death from Electrocution; Sold by HEZI HOME
Consumer productReported January 16, 2026 · The power strips have an ungrounded metal enclosure that poses an electrocution hazard if energized, resulting in serious injury or death. - Morgan Lane Recalls Children's Pajama Sets Due to Risk of Serious Injury or Death from Burn Hazard; Violate Mandatory Flammability Standards for Children's Sleepwear
Consumer productReported January 16, 2026 · The recalled children's pajamas violate the mandatory standards for flammability of children's sleepwear, posing a risk of serious injury and deadly burn... - Adams Manufacturing Recalls Adirondack Patio Chairs Due to Injury and Fall Hazards
Consumer productReported January 16, 2026 · The recalled chairs can crack and collapse, posing injury and fall hazards. - Yixing Trading Recalls KEAWIS Crib Mattresses Due to Risk of Serious Injury or Death from Entrapment and Suffocation; Violates Mandatory Standard for Crib Mattresses
Consumer productReported January 16, 2026 · The aftermarket mattresses violate the mandatory standard for crib mattresses, as the mattresses may not adequately fit certain play yards or non-full-sized... - R.X.Y Bicycle Helmets Recalled Due to Risk of Serious Injury or Death from Head Injury; Violates Mandatory Standard for Bicycle Helmets
Consumer productReported January 16, 2026 · The recalled helmets violate the mandatory safety standard for bicycle helmets because the helmets do not comply with the impact attenuation, positional... - BBWOO Baby Loungers Recalled Due to Risk of Serious Injury or Death from Head Injury; Violates Mandatory Standard for Bicycle Helmets
Consumer productReported January 16, 2026 · The recalled baby loungers violate the mandatory safety standard for Infant Sleep Products. The sides are too low to contain an infant and the enclosed... - Energizer Recalls Rechargeable Lanterns Due to Overheating
Consumer productReported January 16, 2026 · The lithium-ion batteries installed in the lanterns can overheat, posing a burn hazard to consumers. - Ruahouine Hair Growth Serum Bottles Recalled Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging; Sold on Amazon by Ruahouine
Consumer productReported January 16, 2026 · The serum bottles contain minoxidil, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The serum's packaging is... - Sysco Imperial Potato Tater Barrel recall (McCain Foods USA Inc)
FoodClass IIReported January 14, 2026 · Clear hard plastic fragments. - Ore-Ida Tater Tots shaped potatoes recall (McCain Foods USA Inc)
FoodClass IIReported January 14, 2026 · Clear hard plastic fragments. - Locatelli Grated Pecorino Romano 48/8oz Shipper recall (Ambriola Co., Inc., The)
FoodClass IReported January 14, 2026 · Product tested positive for Listeria Monocytogenes. - Ambriola Piccante grated Pecorino Romano recall (Ambriola Co., Inc., The)
FoodClass IReported January 14, 2026 · Product tested positive for Listeria Monocytogenes. - Boar's Head Pecorino Romano Grated recall (Ambriola Co., Inc., The)
FoodClass IReported January 14, 2026 · Product tested positive for Listeria Monocytogenes. - Sam's Pecorino Romano grated recall (Ambriola Co., Inc., The)
FoodClass IReported January 14, 2026 · Product tested positive for Listeria Monocytogenes. - Boar's Head Grated Pecorino Romano recall (Ambriola Co., Inc., The)
FoodClass IReported January 14, 2026 · Product tested positive for Listeria Monocytogenes. - Pinna Grated Pecorino Romano 2/10 recall (Ambriola Co., Inc., The)
FoodClass IReported January 14, 2026 · Product tested positive for Listeria Monocytogenes. - Locatelli Grated Pecorino Romano recall (Ambriola Co., Inc., The)
FoodClass IReported January 14, 2026 · Product tested positive for Listeria Monocytogenes. - Locatelli Grated Pecorino Romano 4 oz and 8 oz plastic cup & lid recall (Ambriola Co., Inc., The)
FoodClass IReported January 14, 2026 · Product tested positive for Listeria Monocytogenes. - Tita Crackers Rovira recall (Rovira Biscuit Corporation)
FoodClass IIReported January 14, 2026 · Undeclared colors FD&C Yellow #6, and FD&C Red 40 - Vainilla Crackers recall (Rovira Biscuit Corporation)
FoodClass IIReported January 14, 2026 · Undeclared colors FD&C Yellow #6, and FD&C Red 40 - Vanilla Treats Crackers recall (Rovira Biscuit Corporation)
FoodClass IIReported January 14, 2026 · Undeclared colors FD&C Yellow #6, and FD&C Red 40 - Vanilla Econo recall (Rovira Biscuit Corporation)
FoodClass IIReported January 14, 2026 · Undeclared colors FD&C Yellow #6, and FD&C Red 40 - Tempting Crackers Tray recall (Rovira Biscuit Corporation)
FoodClass IIReported January 14, 2026 · Undeclared colors FD&C Yellow #6, and FD&C Red 40 - Snack Crackers 100to en boca recall (Rovira Biscuit Corporation)
FoodClass IIReported January 14, 2026 · Undeclared colors FD&C Yellow #6, and FD&C Red 40 - Codman CereLink ICP Sensor Basic Kit. Catalog Number: 826850. The Codman CereLink... recall (Integra LifeSciences Corp. (NeuroSciences))
Medical deviceClass IIReported January 14, 2026 · Potential corrosion stains on the surface of the 14-gauge Tuohy Needle that is included in the Microsensor and Cerelink ICP Kits. - Codman Microsensor Basic Kit. Catalog Number: 626631US. Use of the CODMAN... recall (Integra LifeSciences Corp. (NeuroSciences))
Medical deviceClass IIReported January 14, 2026 · Potential corrosion stains on the surface of the 14-gauge Tuohy Needle that is included in the Microsensor and Cerelink ICP Kits. - The Pressio 2 ICP Monitoring System recall (Sophysa)
Medical deviceClass IIReported January 14, 2026 · Customer complaints of Pressio monitor rebooting. - BD Pyxis ES Enterprise Server Catalog Numbers 1115-00 recall (CareFusion 303, Inc.)
Medical deviceClass IIReported January 14, 2026 · Due a software issue that may result in equipment not receiving timely updates of patient, medication, or related information from enterprise systems. - Philips Tempus Pro Patient Monitor recall (Remote Diagnostic Technologies Ltd.)
Medical deviceClass IIReported January 14, 2026 · Patient monitor measures Intracranial Pressure (ICP) and Bladder Pressure (BDR) but ICP and BDR measurements have not been tested or validated for accuracy. If... - The Elecsys Anti-TSHR immunoassay is a three-step competitive immunoassay with... recall (Roche Diagnostics Operations, Inc.)
Medical deviceClass IIReported January 14, 2026 · Issues identified: 1) Results vary by Instrument Platform; 2) Calibrator Lot-to-Lot Variability. Issues may lead to delayed or incorrect diagnosis, as well as... - Baraka Gourmet Pastry Kunafe 6.7oz. recall (ZIYAD BROTHERS IMPORTING)
FoodClass IIReported January 14, 2026 · May contain partially hydrogenated oils - Baraka French Style Puff Pastry 1lb and 1.5lbs sizes recall (ZIYAD BROTHERS IMPORTING)
FoodClass IIReported January 14, 2026 · May contain partially hydrogenated oils - Rosuvastatin Tablets recall (AvKARE)
DrugClass IIReported January 14, 2026 · Out of specification for dissolution.