State

Texas product recalls

73,509 recalls have nationwide distribution and so reach Texas. 12,437 additional recalls listed Texas specifically in their distribution scope.

What the numbers show

Total: 12,437
Critical: 1,720
Severe: 2,926
Most recent: 2026-10-14

Of the 12,437 recalls naming Texas we have scored against our rubric, 1,720 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,926 (24%) are Severe.

Which agencies issued them

These figures cover only the 12,437 recalls whose distribution notice names Texas specifically. The 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

26326–26350 of 85946

HighFDA (Devices)·Z-0164-2022·2021-11-03
Gore CARDIOFORM Septal Occluder recalled for incorrect expiration date
W.L. Gore & Associates is recalling 2,238 GORE CARDIOFORM SEPTAL OCCLUDER 30 mm devices labeled with a 3-year expiration date instead of the actual 2-year expiration date.
Product
REF/Catalogue Number GSX0030A, GORE CARDIOFORM SEPTAL OCCLUDER 30 mm Diameter, Catheter Working Length 75 cm, Delivery Profile 10 Fr, STERILE EO, Rx Only, UDI: 00733132631032
Category
Medical Device
Distribution
47 states
HighFDA (Drugs)·D-0056-2022·2021-11-03
Calcium Gluconate 10% Injectable Recalled for Sterility Assurance
Red Mountain Compounding Pharmacy is recalling Calcium Gluconate 10% Injectable (PF) due to lack of assurance of sterility following an FDA inspection. The product was distributed to approximately 494 patients across seven states.
Product
CALCIUM GLUCONATE 10% INJ (PF), Rx only, Red Mountain Compounding Rx
Category
Drug
Distribution
7 states
HighFDA (Devices)·Z-0179-2022·2021-11-03
BD Syringe Tip Cap Packaging Defect May Compromise Sterility
Becton Dickinson & Company is recalling BD Syringe Tip Caps (Catalog Number 305822, Lot 1111347) due to holes in the packaging that may compromise sterility and container closure integrity.
Product
BD Syringe Tip Cap Bulk Sterile Convenience Pak-1000 units/shelf carton. Used to seal syringes and maintain container closure integrity throughout the shelf life of the BD WWD syringe. Catalog Number: 305822
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-0177-2022·2021-11-03
Bivona Aire-Cuf Endotracheal Tubes Recalled for Compromised Sterile Barrier
Smiths Medical is recalling 7136 Bivona Aire-Cuf Endotracheal Tubes due to inadequate pouch seals that compromise the sterile barrier. The issue affects specific lot numbers with 325mm shaft length.
Product
Bivona Aire-Cuf Endotracheal Tube
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0178-2022·2021-11-03
Bivona Uncuffed Endotracheal Tubes Recalled for Compromised Sterile Barrier
Smiths Medical ASD Inc. is recalling 2,191 Bivona Uncuffed Wire Endotracheal Tubes due to inadequate pouch seals that compromise the sterile barrier. Affected devices have 325mm shaft lengths and were distributed nationwide and internationally.
Product
Bivona Uncuffed Wire Endotracheal Tubes,
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0170-2022·2021-11-03
GORE CARDIOFORM Septal Occluder Recalled for Incorrect Expiration Date Labeling
W L Gore & Associates is recalling 187 units of GORE CARDIOFORM Septal Occluders because they are labeled with a 3-year expiration date instead of the correct 2-year expiration date. Using the device beyond its actual shelf life could compromise its safety and effectiveness.
Product
REF/Catalogue Number GSXE0025B, GORE CARDIOFORM SEPTAL OCCLUDER 25 mm Diameter, Catheter Working Length 75 cm, Delivery Profile 10 Fr, STERILE EO, Rx Only, UDI: 00733132620111 *Not distributed within the US
Category
Medical Device
Distribution
47 states
HighFDA (Devices)·Z-0175-2022·2021-11-03
Cliquid MD Software Version 3.4 May Provide Incorrect Analytical Results
AB SCIEX's Cliquid MD version 3.4 software may incorrectly calculate Internal Standard concentrations when users hide or leave the IS column empty in customized LC-MS/MS tests, potentially leading to incorrect analytical conclusions.
Product
Cliquid MD version 3.4 software used in conjunction with Analyst MD software on SCIEX Citrine & 4500MD series liquid chromatography-tandem mass spectrometry (LC-MS/MS) systems. Model No. 5088288
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0067-2022·2021-11-03
Simple Mills Almond Flour Crackers Recalled for Undeclared Milk Allergen
Simple Mills has recalled Almond Flour Crackers with fine ground sea salt because they contain undeclared milk allergen. The product was distributed across 36 states.
Product
Almond Flour Crackers fine ground sea salt packaged in a white box with yellow graphics weighing 4.25 oz. Label reads "***Simple Mills***Almond Flour crackers Fine Ground Sea Salt***Net wT 4.25 oz***" UPC: 856069005131
Category
Food
Distribution
37 states
ModerateFDA (Drugs)·D-0079-2022·2021-11-03
Rizatriptan Benzoate Tablets Recalled for Out-of-Specification Impurities
Macleods Pharma USA is recalling Rizatriptan Benzoate 5mg orally disintegrating tablets nationwide due to out-of-specification results in organic impurities testing. The affected lots are BRL2102A and BRL2103A with expiration date 04/2025.
Product
RIZATRIPTAN BENZOATE — RIZATRIPTAN BENZOATE (RIZATRIPTAN BENZOATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0172-2022·2021-11-03
Septal Occluder Devices Recalled for Incorrect Expiration Date Labeling
W L Gore & Associates recalls GORE CARDIOFORM SEPTAL OCCLUDER devices labeled with a 3-year expiration date when the actual shelf life is 2 years. The mislabeling affects 15 units distributed across the United States and internationally.
Product
REF/Catalogue Number GSX0030H, GORE CARDIOFORM SEPTAL OCCLUDER 30 mm Diameter, Catheter Working Length 75 cm, Delivery Profile 10 Fr, STERILE EO, Rx Only, UDI: 00733132648948 *Not distributed within the US
Category
Medical Device
Distribution
47 states
ModerateCPSC·22015·2021-11-03
Elektron BP-1 Power Handles Recalled for Fire and Burn Hazards
Elektron Power Handle BP-1 units can short circuit and overheat, creating fire and burn risks. Consumers should stop using them immediately and contact Elektron for a full refund.
Product
Elektron BP-1 Power Handles
Category
Consumer Product
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0091-2022·2021-11-03
Gatifloxacin Ophthalmic Solution Recalled for Failed Stability Tests
Lupin Pharmaceuticals is recalling Gatifloxacin Ophthalmic Solution 0.5% due to failed water loss tests that may affect drug concentration. The recall affects 16,272 bottles distributed nationwide.
Product
Gatifloxacin Ophthalmic Solution, 0.5%, 2.5 mL bottle, Rx only, Manufactured by: Lupin Limited, Pithampur (M.P.) 454 775, INDIA, NDC 68180-435-01.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0034-2022·2021-11-03
Cyclosporin 0.2% Oil Ophthalmic Suspension Recall Due to Sterility Assurance
Red Mountain Compounding Pharmacy is recalling Cyclosporin 0.2% Oil Ophthalmic Suspension because FDA inspection identified concerns about sterility assurance. The recalled drug was distributed to approximately 494 patients across multiple states.
Product
CYCLOSPORIN 0.2% OIL OPTH SUSP, Rx only, Red Mountain Compounding Rx
Category
Drug
Distribution
7 states
ModerateFDA (Drugs)·D-0067-2022·2021-11-03
Sodium Selenite Injectable Solution Recalled for Sterility Concerns
Red Mountain Compounding Pharmacy is recalling Sodium Selenite 200mcg/ml injectable solution due to FDA inspection findings regarding lack of assurance of sterility. Approximately 494 patients in seven states received prescriptions for this product.
Product
SODIUM SELINITE 200MCG/ML FOR INJ, Rx only, Red Mountain Compounding Rx
Category
Drug
Distribution
7 states
ModerateFDA (Drugs)·D-0077-2022·2021-11-03
Afassco Pain Free Plus X-Strength Tablets Recalled for Failed Stability
Ultra Seal Corporation is recalling Afassco Pain Free Plus X-Strength Pain Reliever tablets nationwide due to out-of-specification results for Salicylic Acid, a related compound of Aspirin, indicating failed stability testing.
Product
Afassco Pain Free Plus X-STRENGTH PAIN RELIEVER (Acetaminophen 250 mg/Aspirin 250 mg/Caffeine 65 mg) tablets, 2 Tablets/package, Packaged in 12,000 Packets/Case, PO# 19540, Mfg. for: Afassco Minden, NV 89423 (Shipping Label)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0064-2022·2021-11-03
MIC/B12A/B6 Injection Recalled for Sterility Assurance Concerns
Red Mountain Compounding Pharmacy is recalling MIC/B12A/B6 injectable medication because FDA inspection identified concerns about sterility assurance. The recall affects 494 patients across seven states.
Product
MIC/B12A/B6 15/50/100 5MG/50MG/ML MDV, Rx only, Red Mountain Compounding Rx
Category
Drug
Distribution
7 states
ModerateFDA (Drugs)·D-0078-2022·2021-11-03
Rizatriptan Benzoate Tablets Recall Due to Out-of-Specification Impurities
MacLeods Pharma USA is recalling Rizatriptan Benzoate Film Coated Tablets (10 mg) due to out-of-specification test results in organic impurities testing. The recall affects multiple lot numbers distributed nationwide.
Product
RIZATRIPTAN — RIZATRIPTAN (RIZATRIPTAN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0029-2022·2021-11-03
Magnesium Chloride Injection Recalled for Sterility Assurance Concerns
Red Mountain Compounding Pharmacy is recalling Magnesium Chloride 200 mg/mL injection because FDA inspection raised concerns about lack of assurance of sterility. The product was distributed to approximately 494 patients in seven states.
Product
Magnesium Chloride, 200 mg/mL MDV INJ, Rx only, Red Mountain Compounding Rx
Category
Drug
Distribution
7 states
ModerateFDA (Drugs)·D-0076-2022·2021-11-03
Xpect First Aid Extra Strength Pain Away tablets recalled for failed stability specifications
Ultra Seal Corporation is recalling Xpect First Aid Extra Strength Pain Away tablets nationwide due to out-of-specification results for Salicylic Acid, a compound related to Aspirin, indicating failed stability testing.
Product
Xpect First aid Extra Strength PAIN AWAY (Acetaminophen 250 mg/Aspirin 250 mg/Caffeine 65 mg) tablets, 2 Tablets/package, Packaged in 12,000 Packets/Case, Material# 111519, Mfg. for: Cintas First Aid & Safety, Mason, OH 45040 (Shipping Label)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0075-2022·2021-11-03
Advance Formula Pain Reliever tablets recalled for failed stability specifications
Ultra Seal Corporation is recalling Advance Formula Pain Reliever tablets (Acetaminophen 250 mg/Aspirin 250 mg/Caffeine 65 mg) distributed nationwide due to out-of-specification results for Salicylic Acid, an Aspirin-related compound.
Product
Advance Formula Pain Reliever (Acetaminophen 250 mg/Aspirin 250 mg/Caffeine 65 mg) tablets, 2 tablets Per Packet, Packaged in 12,000 Packets/Case, PO# 007564-00, Item# 1170, Mfg. for: Advanced First Aid, Baltimore, MD 21237; American Safety & First Aid, Osceola, IN 46561…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0074-2022·2021-11-03
North by Honeywell Pain Stopper Extra Strength tablets recalled for failed stability
Ultra Seal Corporation is recalling North by Honeywell Pain Stopper Extra Strength tablets nationwide because stability testing found out-of-specification results for Salicylic Acid, an aspirin-related compound.
Product
North by Honeywell PAIN STOPPER EXTRA STRENGTH (Acetaminophen 250 mg, Aspirin 250 mg, Caffeine 65 mg) tablets, 2 tablets per packet, Packaged in 5,000 Packets/Case, PO# B121242, Item# 853500-01, Dist. By Honeywell Safety Products USA, Smithfield, RI 02917
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0168-2022·2021-11-03
GORE CARDIOFORM Septal Occluder Labeled with Incorrect Expiration Date
W L Gore & Associates is recalling GORE CARDIOFORM Septal Occluder devices labeled with a 3-year expiration date instead of the correct 2-year date. Mislabeling could result in use of devices beyond their intended safe lifespan.
Product
REF/Catalogue Number GSXE0025, GORE CARDIOFORM SEPTAL OCCLUDER 25 mm Diameter, Catheter Working Length 75 cm, Delivery Profile 10 Fr, STERILE EO, Rx Only, UDI: 00733132617647 *Not distributed within the US
Category
Medical Device
Distribution
47 states
ModerateFDA (Drugs)·D-0060-2022·2021-11-03
Methylcobalamin injection recalled due to sterility assurance concerns
Red Mountain Compounding Pharmacy is recalling a methylcobalamin injectable solution after FDA inspection raised concerns about the lack of assurance of sterility.
Product
METHYLCOBALAMIN 12.5MG/ML MDV INJ SOLN, Rx only, Red Mountain Compounding Rx
Category
Drug
Distribution
7 states
ModerateFDA (Drugs)·D-0073-2022·2021-11-03
AERO Tab Pain Reliever Tablets Recalled for Failed Stability Specifications
Ultra Seal Corporation is recalling AERO Tab Pain Reliever tablets nationwide because out-of-specification results were found for Salicylic Acid, an Aspirin-related compound, indicating failed stability testing.
Product
AERO Tab PAIN RELIEVER (Acetaminophen 250 mg/Aspirin 250 mg/Caffeine 65 mg) tablets , 2 tablets Per Packet, Packaged in 10,000 Packets/Case, PO# 11938, Mfg. for: Aero Healthcare, Valley Cottage, NY 10989 (Shipping Label )
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0068-2022·2021-11-03
Loratadine-D Extended-Release Tablets Recalled for Failed Moisture Limits
Sun Pharmaceutical Industries is recalling 22,752 blister packs of Loratadine-D Extended-Release Tablets (10mg/240mg) distributed nationwide due to failed moisture limits. The affected lot is AC14635 with expiration date 12/2022.
Product
LORATADINE AND PSEUDOEPHEDRINE SULFATE — LORATADINE AND PSEUDOEPHEDRINE SULFATE (LORATADINE AND PSEUDOEPHEDRINE SULFATE)
Category
Drug
Distribution
Distributed nationwide