Shortage: Ketorolac Tromethamine Injection — Ketorolac Tromethamine, Injection, 30 mg/1 mL (NDC 25021-701-01) Status: Current Used for: Analgesia/Addiction

Shortage: Clindamycin Phosphate Injection — Clindamycin Phosphate, Injection, 150 mg/1 mL (NDC 25021-115-06) Status: Current Reason: Discontinuation of the manufacture of the drug Used for: Anti-Infective

Benzoyl Peroxide Wash, USP, 10%, packaged in a)5 FL OZ (148mL) bottles (NDC 0536-1261-63), and b) 8.5 FL OZ (237 mL) bottles (NDC 0536-1351-42), Distributed by: Rugby Laboratories, 17177 N. Laurel Park Drive, Suite 233, Livonia, MI 48152. Reason: Microbial contamination of topical product. Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongoing · IL only

Estradiol Gel, 0.1%, 0.25 mg, 30-packets per carton, Rx only, Distributed by: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08907, NDC 69238-2452-3. Reason: Defective Container; packets were found to be either empty or partially full. Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongoing · Nationwide in the USA.

FOCUS PI Hypromellose 0.7% Formula, 0.3 FL O (10 mL) per vial, STERILE, Manufactured for: Covalent Management, Inc., Manassas, VA 20109. NDC: 82724-007-19 Reason: Lack of Assurance of Sterility Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongoing · VA

Zoladex (goserelin) implant, 3.6 mg, One single-Use Syringe17 reports about syringe on this site. See them all → packaged in a carton, Rx only, Manufactured for: TerSera therapeutics LLC, Deerfield, IL 60015, BY: AstraZeneca UK Limited, Macclesfield, England, Product of Switzerland, website at www.zoladex.com, NDC 70720-950-36. Reason: Temperature Abuse: Product sat in a non-temperature-controlled FedEx trail…

Paroxetine Extended-Release Tablets, 37.5mg, 30-count bottle, Rx only, Manufactured by: Apotex Inc., Toronto, Ontario, Canada M9L 1T9, Manufactured for: Apotex Corp., Weston, Florida 33326, NDC 60505-1318-3 Reason: Failed dissolution specifications. Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongoing · US Nationwide.

Benzoyl Peroxide Wash, USP, 5%, 5 FL OZ (148 mL), Distributed by: Rugby Laboratories, 17177 N. Laurel Park Drive, Suite 233, Livonia, MI 48152. NDC: 0536-1259-63 Reason: Microbial contamination of topical product. Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongoing · IL only

Buprenorphine Hydrochloride, Injection 0.3 mg/mL, Rx Only, 5 x 1 mL Single Dose Vials, Manufactured for: Endo USA, Malvern, PA, NDC 42023-179-05 Reason: Crystallization Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongoing · U.S. Nationwide

Ranolazine Extended-Release Tablets, 1000 mg, 60-count bottle, Rx Only, Marketed by: Ajanta Pharma USA Inc., Bridgewater, NJ 08807. NDC: 27241-126-02 Reason: Failed Dissolution Specifications: below specification Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongoing · Nationwide in the US.

Nova Biomedical® Announces Global Medical Device Correction for StatStrip® Glucose Hospital Meter WALTHAM, Mass., October 5, 2026 – Nova Biomedical initiated a global Medical Device Correction on July 24, 2026, for the StatStrip® Glucose Hospital Meter System due to a software issue that may cause a glucose result to be associated with the wrong patient. Wh…

IV Tubing Set Correction: ICU Medical Updates Use Instructions for IV Tubing Sets Black specks and particulate reported in drip chambers of certain ICU Medical IV tubing sets does not affect device safety, performance, or intended use.

Breathing Circuit RecallThe maker or a government agency pulled this product. Check the model or lot number and stop using it until it's fixed or refunded.: Draeger Removes VentStar Resus Neo Hoses Removal of VentStar Resus Neo hoses due to the potential for cracks resulting in restricted ventilation or delayed therapy.

Shortage: Amphetamine Aspartate Monohydrate, Amphetamine Sulfate, Dextroamphetamine Saccharate, Dextroamphetamine Sulfate Tablet — Amphetamine Aspartate Monohydrate, Amphetamine Sulfate, Dextroamphetamine Saccharate, Dextroamphetamine Sulfate, Tablet, 3.75 mg; 3.75 mg; 3.75 mg; 3.75 mg (NDC 13107-072-01) Status: Current Reason: Shortage of an active ingredi…

Greenwich Rx Issues Voluntary Nationwide RecallThe maker or a government agency pulled this product. Check the model or lot number and stop using it until it's fixed or refunded. of Compounded Glutathione Due to Elevated Endotoxin Levels IMMEDIATE RELEASE - Tomball, Texas – October 1, 2026 – Greenwich Rx, a 503A compounding pharmacy, is voluntarily recalling specific lots of its compounded glutathione to the consumer level. The product is being recalled due to potential elevated endoto…

Shortage: Dexmedetomidine Hydrochloride Injection — Dexmedetomidine Hydrochloride, Injection, 4 ug/1 mL (NDC 44567-602-24) Status: Current Used for: Anesthesia

TRP The Relief Products* Gentle Eyes Lubricant Eye Drops18 reports about eye drop on this site. See them all →, Carboxymethylcellulose sodium 0.5%, Sterile Eye Drops, 0.5 FL OZ (15 mL) bottles, Manufactured exclusively for TRP Company, Inc. 1575 Delucci Ln, Reno, NV 89502, NDC 17312-430-15. Reason: Lack of Assurance of Sterility Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongoing · USA Nationwide

AvKare Carboxymethylcellulose Sodium Ophthalmic Solution 0.5%, Lubricant Eye Drops18 reports about eye drop on this site. See them all →, Sterile, 0.5 FL OZ (15 mL) EACH, 1.0 FL OZ (30 mL) TOTAL, 2 count Twin Pack, Distributed by: AVKARE, Pulaski, TN, 38478, NDC 50268-068-02 (carton) Reason: Lack of Assurance of Sterility Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongoing · USA Nationwide

Clear Eyes Redness Relief, Lubricant/Redness Reliever Eye Drops18 reports about eye drop on this site. See them all → (glycerin 0.25%, naphazoline hydrochloride 0.012%) with Hang Tag, 0.5 fl oz (15mL) per dropper bottle, STERILE, Dist. by Medtech Products Inc., Tarrytown, NY 10591. NDC: 67172-797-15 Reason: Lack of Assurance of Sterility Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongoing · Nationwide in the USA.

AvKare Carboxymethylcellulose Sodium Ophthalmic Solution 0.5%, Lubricant Eye Drops18 reports about eye drop on this site. See them all →, Sterile, 0.5 FL OZ (15 mL) bottle, Distributed by: AVKARE, Pulaski, TN, 38478, NDC 50268-068-15 Reason: Lack of Assurance of Sterility Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongoing · USA Nationwide

Lubricant Eye Drops18 reports about eye drop on this site. See them all →-Cameron Pharmaceuticals, Carboxymethylcellulose Sodium 0.5%, Eye Lubricant, 0.5 FL OZ (15 mL) bottles, Distributed by Cameron Pharmaceuticals, LLC, Louisville, KY, 40245, NDC 42494-448-05 Reason: Lack of Assurance of Sterility Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongoing · USA Nationwide

Reliable -1 Laboratories, Sodium Chloride Hypertonicity Ophthalmic Solution, 5%, Sterile, 0.5 FL OZ (15 mL) bottles, Distributed by: Reliable-1 Laboratories LLC, Valley Stream, NY, 11580, NDC 69618-077-55. Reason: Lack of Assurance of Sterility Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongoing · USA Nationwide

Walgreens Lubricant Eye Drops18 reports about eye drop on this site. See them all →, 0.5 FL OZ (15 mL) 1.0 FL OZ (30 mL) TOTAL, 2 count Twin Pack, Distributed by Walgreens Co., 200 Wilmot Road, Deerfield, IL 60015, NDC 0363-8833-15. Reason: Lack of Assurance of Sterility Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongoing · USA Nationwide

Exenatide Injection, USP, 250 mcg/mL, 1.2 mL per prefilled pen, Rx Only, Subcutaneous Use Only, For Single Patient Use Only, Manufactured by: Amneal Pharmaceuticals Pvt. Ltd., Ahmedabad 382213, India; Distributed by: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807, NDC 70121-1685-1 Reason: Defective Delivery System: Possibility of no medication in the pre…

Olanzapine Tablets, USP 5 mg, 30-count bottle, Rx Only, Manufactured For: Macleods Pharma USA, Inc. Princeton, NJ, 08540; Manufactured by: Macleods Pharmaceuticals, Ltd, Baddi, Himachal Pradesh, INDIA, NDC 33342-068-07. Reason: Failed Impurities/Degradation Specifications:Organic and unspecified impurities above specification. Class IIIThe lowest FDA recall level: unlikely to cause health problems, but it breaks the rules. · Ongoing · Nationwi…

Major LubriFresh P.M. Nighttime Ointment3 reports about ointment on this site. See them all →, Net wt. 0.125 oz. (3.5 g) tubes, Distributed by: Major Pharmaceuticals, 17177 N Laurel Park Drive, Suite 233, Livonia, MI 48152, NDC 0904-6488-38 Reason: Lack of Assurance of Sterility Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongoing · USA Nationwide

Walgreens Lubricant Eye Drops18 reports about eye drop on this site. See them all →, Carboxymethylcellulose sodium 0.5%, Lubricant Eye Drops, Sterile, 0.5 OZ (15 mL) bottles, Distributed by Walgreen Co., 200 Wilmot Rd., Deerfield, IL 60015, NDC 0363-8833-15. Reason: Lack of Assurance of Sterility Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongoing · USA Nationwide

Clear Eyes Redness Relief, Lubricant/Redness Reliever Eye Drops18 reports about eye drop on this site. See them all → (glycerin 0.25%, naphazoline hydrochloride 0.012%) , 0.5 fl oz (15mL) per dropper bottle, STERILE, Dist. by Medtech Products Inc., Tarrytown, NY 10591. NDC: 67172-797-15 Reason: Lack of Assurance of Sterility Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongoing · Nationwide in the USA.

Reliable-1 Laboratories Lubricating Tears, Sterile, 0.5 FL OZ (15 mL) bottles, Distributed by: Reliable-1 Laboratories LLC, Valley Stream, NY, 11580, www.reliable1labs.com, NDC 69618-076-55. Reason: Lack of Assurance of Sterility Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongoing · USA Nationwide

MENOW SUNSCREEN PRESSED POWDER SPF35 PA+++, Net content, 9g/0.32 oz, Manufactured by: Shantzu Qiwei Industry Co. Ltd, Add: Quiwei Building, Yingloinguan, Xiashan, Chaonan district, Shantou City, Guangdong Province, China Reason: cGMP Deviations Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongoing · CA only