Drug Recall
Terminated
Historical recordClass II
Dr. Reddy's Ezetimibe and Simvastatin Tablets, 10 mg/10 mg, a) 90 count (NDC 43598-742-90) and b) 1000 count (NDC 43598-742-10) bottles, Rx only, Manufactured by: Dr. Reddy's Laboratories LA LLC, Shreveport, LA 71106, USA, Distributed by: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540 USA, , packaged in bottles.
by Dr. Reddy's Laboratories, Inc.
- Reason
- Failed Excipient Specifications; product manufactured using an excipient found to be OOS for conductivity
- Recall initiated
- October 5, 2021
- Reported by FDA
- November 10, 2021
- Distribution
- Nationwide in the US
View recall →
Drug Recall
Terminated
Historical recordClass III
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.
by Lupin Pharmaceuticals Inc.
- Reason
- Failed Stability Specifications: Out-of-specification results observed in a water loss test that might affect the assay content and alter drug concentration.
- Recall initiated
- October 20, 2021
- Reported by FDA
- November 3, 2021
- Distribution
- Nationwide in the USA and Puerto Rico
View recall →
Drug Recall
Terminated
Historical recordClass III
Rizatriptan Benzoate Orally Disintegrating Tablets 10mg, 18 Tablets (3 x 6 Unit-Dose Tablets) Blister Packs, Rx only, Manufactured for: Macleods Pharma USA Inc. Plainsboro, NJ 08536, Manufactured by: Macleods Pharmaceuticals Ltd. Baddi, Himachal Pradesh, INDIA, NDC 33342-094-41
by MACLEODS PHARMA USA, INC
- Reason
- Out-of-specification test results obtained in Organic Impurities test during analysis of controlled samples.
- Recall initiated
- October 18, 2021
- Reported by FDA
- November 3, 2021
- Distribution
- Nationwide within the United States
View recall →
Drug Recall
Terminated
Historical recordClass III
Rizatriptan Benzoate Orally Disintegrating Tablets 5mg, 12 Tablets (2 x 6 Unit-Dose Tablets) Blister Packs, Rx only, Manufactured for: Macleods Pharma USA Inc. Plainsboro, NJ 08536, Manufactured by: Macleods Pharmaceuticals Ltd. Baddi, Himachal Pradesh, INDIA, NDC 33342-093-41
by MACLEODS PHARMA USA, INC
- Reason
- Out-of-specification test results obtained in Organic Impurities test during analysis of controlled samples.
- Recall initiated
- October 18, 2021
- Reported by FDA
- November 3, 2021
- Distribution
- Nationwide within the United States
View recall →
Drug Recall
Terminated
Historical recordClass III
Rizatriptan Benzoate Film Coated Tablets, 10 mg, packaged in a) 12 Tablets (2X6 Unit-Dose Tablets) Blister Packs, NDC 33342-088-45), b) 18 Tablets (3 x 6 Unit-Dose Tablets, NDC 33342-088-41) Rx only, Manufactured for: Macleods Pharma USA, Inc. Plainsboro, NJ 08536l Manufactured by: Macleods Pharmaceuticals Ltd. Baddi, Himachal Pradesh, INDIA
by MACLEODS PHARMA USA, INC
- Reason
- Out-of-specification test results obtained in Organic Impurities test during analysis of controlled samples.
- Recall initiated
- October 18, 2021
- Reported by FDA
- November 3, 2021
- Distribution
- Nationwide within the United States
View recall →
Drug Recall
Terminated
Historical recordClass III
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)
by Ultra Seal Corporation
- Reason
- Failed Stability Specifications: Out-of-Specification results observed for Aspirin related compound Salicylic Acid.
- Recall initiated
- October 13, 2021
- Reported by FDA
- November 3, 2021
- Distribution
- Nationwide in the USA.
View recall →
Drug Recall
Terminated
Historical recordClass III
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)
by Ultra Seal Corporation
- Reason
- Failed Stability Specifications: Out-of-Specification results observed for Aspirin related compound Salicylic Acid.
- Recall initiated
- October 13, 2021
- Reported by FDA
- November 3, 2021
- Distribution
- Nationwide in the USA.
View recall →
Drug Recall
Terminated
Historical recordClass III
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 (Shipping Label)
by Ultra Seal Corporation
- Reason
- Failed Stability Specifications: Out-of-Specification results observed for Aspirin related compound Salicylic Acid.
- Recall initiated
- October 13, 2021
- Reported by FDA
- November 3, 2021
- Distribution
- Nationwide in the USA.
View recall →
Drug Recall
Terminated
Historical recordClass III
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
by Ultra Seal Corporation
- Reason
- Failed Stability Specifications: Out-of-Specification results observed for Aspirin related compound Salicylic Acid.
- Recall initiated
- October 13, 2021
- Reported by FDA
- November 3, 2021
- Distribution
- Nationwide in the USA.
View recall →
Drug Recall
Terminated
Historical recordClass III
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 )
by Ultra Seal Corporation
- Reason
- Failed Stability Specifications: Out-of-Specification results observed for Aspirin related compound Salicylic Acid.
- Recall initiated
- October 13, 2021
- Reported by FDA
- November 3, 2021
- Distribution
- Nationwide in the USA.
View recall →
Drug Recall
Terminated
Historical recordClass III
ZEE+ painaid ESF Extra-Strength Formula (Acetaminophen 250 mg, Aspirin 250 mg (NSAID), Caffeine 65 mg) tablets, 2 Tablets per/package, Packaged in a) 50-count packages/carton, b) 125-count packages/carton, PA-ESF 1414Z, Dist. by: Zee Medical Distributors, LLC Mason, OH 45040 (Shipping Label)
by Ultra Seal Corporation
- Reason
- Failed Stability Specifications: Out-of-Specification results observed for Aspirin related compound Salicylic Acid.
- Recall initiated
- October 13, 2021
- Reported by FDA
- November 3, 2021
- Distribution
- Nationwide in the USA.
View recall →
Drug Recall
Terminated
Historical recordClass III
Vica-Cet BACK PAIN RELIEF (Acetaminophen 250 mg/Aspirin 250 mg/Caffeine 65 mg) tablets, 2 tablets/pk, packaged in 10,000 packets, PO# 8967, Mfg. for Tellus/The Provision First Aid Line (Shipping Label)
by Ultra Seal Corporation
- Reason
- Failed Stability Specifications: Out-of-Specification results observed for Aspirin related compound Salicylic Acid.
- Recall initiated
- October 13, 2021
- Reported by FDA
- November 3, 2021
- Distribution
- Nationwide in the USA.
View recall →
Drug Recall
Terminated
Historical recordClass III
PainAway II (Acetaminophen 250 mg/Aspirin 250 mg/Caffeine 65 mg) tablets , 2 tablets/pk, packaged in 12,000 Packets/Case, Material # 11161, Mfg. for Respond Industries First Aid, Mason, OH 45040 (Shipping Label)
by Ultra Seal Corporation
- Reason
- Failed Stability Specifications: Out-of-Specification results observed for Aspirin related compound Salicylic Acid.
- Recall initiated
- October 13, 2021
- Reported by FDA
- November 3, 2021
- Distribution
- Nationwide in the USA.
View recall →
Drug Recall
Terminated
Historical recordClass III
AllerClear D-24 hr, (Loratadine and Pseudoephedrine Sulfate, Extended-Release Tablets, USP 10/240mg), 15-count blister packs, Manufactured by: Ohm Laboratories Inc., 1385 Livingston Avenue, North Brunswick, NJ 08902, NDC 63981-724-15
by SUN PHARMACEUTICAL INDUSTRIES INC
- Reason
- Failed Moisture Limits
- Recall initiated
- October 12, 2021
- Reported by FDA
- November 3, 2021
- Distribution
- Nationwide within the United States
View recall →
Drug Recall
Terminated
Historical recordClass III
Loratadine-D Extended-Release Tablets (Loratadine and Pseudoephedrine Sulfate, Extended-Release Tablets, USP 10mg/240mg) , 10-count blister packs, Distributed By Major Pharmaceuticals, 17177 N Laurel Park Drive, Suite 233, Livonia, MI 48152, NDC 0904-5833-15
by SUN PHARMACEUTICAL INDUSTRIES INC
- Reason
- Failed Moisture Limits
- Recall initiated
- October 12, 2021
- Reported by FDA
- November 3, 2021
- Distribution
- Nationwide within the United States
View recall →
Drug Recall
Terminated
Historical recordClass II
SODIUM SELINITE 200MCG/ML FOR INJ, Rx only, Red Mountain Compounding Rx
by First Royal Care Co. LLC, dba Red Mountain Compounding Pharmacy
- Reason
- Lack of Assurance of Sterility: FDA inspection raised sterility assurance concerns
- Recall initiated
- August 13, 2021
- Reported by FDA
- November 3, 2021
- Distribution
- 494 patients/consumers received prescriptions and are located in AZ, CA FL, MN, MT, TX, and UT.
View recall →
Drug Recall
Terminated
Historical recordClass II
PROGESTERONE 100MG/ML MDV OIL INJECTION, Rx only, Red Mountain Compounding Rx
by First Royal Care Co. LLC, dba Red Mountain Compounding Pharmacy
- Reason
- Lack of Assurance of Sterility: FDA inspection raised sterility assurance concerns
- Recall initiated
- August 13, 2021
- Reported by FDA
- November 3, 2021
- Distribution
- 494 patients/consumers received prescriptions and are located in AZ, CA FL, MN, MT, TX, and UT.
View recall →
Drug Recall
Terminated
Historical recordClass II
MIT/B12 25/50/50MG/ML 1MG/ML MDV, Rx only, Red Mountain Compounding Rx
by First Royal Care Co. LLC, dba Red Mountain Compounding Pharmacy
- Reason
- Lack of Assurance of Sterility: FDA inspection raised sterility assurance concerns
- Recall initiated
- August 13, 2021
- Reported by FDA
- November 3, 2021
- Distribution
- 494 patients/consumers received prescriptions and are located in AZ, CA FL, MN, MT, TX, and UT.
View recall →
Drug Recall
Terminated
Historical recordClass II
MIC/B12A/B6 15/50/100 5MG/50MG/ML MDV, Rx only, Red Mountain Compounding Rx
by First Royal Care Co. LLC, dba Red Mountain Compounding Pharmacy
- Reason
- Lack of Assurance of Sterility: FDA inspection raised sterility assurance concerns
- Recall initiated
- August 13, 2021
- Reported by FDA
- November 3, 2021
- Distribution
- 494 patients/consumers received prescriptions and are located in AZ, CA FL, MN, MT, TX, and UT.
View recall →
Drug Recall
Terminated
Historical recordClass II
MIC/B12A 25/50/50MG/ML 1MG/ML MDV, Red Mountain Compounding Rx
by First Royal Care Co. LLC, dba Red Mountain Compounding Pharmacy
- Reason
- Lack of Assurance of Sterility: FDA inspection raised sterility assurance concerns
- Recall initiated
- August 13, 2021
- Reported by FDA
- November 3, 2021
- Distribution
- 494 patients/consumers received prescriptions and are located in AZ, CA FL, MN, MT, TX, and UT.
View recall →
This information is republished from FDA's Recall Enterprise System through openFDA. Public Health Trace
does not verify or supplement it, is not affiliated with the FDA, and does not provide medical advice --
always follow the guidance of your pharmacist, physician, or the recalling company for any medication you take.
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