FDA daily for Friday, October 9, 2026
55 FDA records across 3 sections. 1 touches MedGrid's categories and is listed first.
Drug shortagesCovers FDA's Thu, Oct 8 (yesterday)1 touch MedGrid22
- Lidocaine Hydrochloride InjectionTouches MedGrid categories
Lidocaine Hydrochloride, Injection, 10 mg/1 mL (NDC 65282-1605-1) — Spectra Medical Devices, LLC
- Clindamycin Phosphate Injection
Clindamycin Phosphate In 5% Dextrose In Plastic Container, Injection, 12 mg/1 mL (NDC 0781-3289-09) — Sandoz Inc.
- Ketorolac Tromethamine Injection
Ketorolac Tromethamine, Injection, 30 mg/1 mL (NDC 25021-701-02) — Sagent Pharmaceuticals
- Clindamycin Phosphate Injection
Clindamycin Phosphate In 5% Dextrose In Plastic Container, Injection, 12 mg/1 mL (NDC 72572-074-24) — Sandoz Inc.
- Ketorolac Tromethamine Injection
Ketorolac Tromethamine, Injection, 30 mg/1 mL (NDC 25021-701-01) — Sagent Pharmaceuticals
- Rocuronium Bromide Injection
Rocuronium Bromide, Injection, 10 mg/1 mL (NDC 25021-687-05) — Sagent Pharmaceuticals
- Amphetamine Aspartate Monohydrate, Amphetamine Sulfate, Dextroamphetamine Saccharate, Dextroamphetamine Sulfate Tablet
Amphetamine Aspartate Monohydrate, Amphetamine Sulfate, Dextroamphetamine Saccharate, Dextroamphetamine Sulfate, Tablet, 5 mg; 5 mg; 5 mg; 5 mg (NDC 0185-0853-01) — Sandoz Inc.
- Clindamycin Phosphate Injection
Clindamycin Phosphate, Injection, 150 mg/1 mL (NDC 25021-115-06) — Sagent Pharmaceuticals
- Amphetamine Aspartate Monohydrate, Amphetamine Sulfate, Dextroamphetamine Saccharate, Dextroamphetamine Sulfate Tablet
Amphetamine Aspartate Monohydrate, Amphetamine Sulfate, Dextroamphetamine Saccharate, Dextroamphetamine Sulfate, Tablet, 1.25 mg; 1.25 mg; 1.25 mg; 1.25 mg (NDC 0185-2098-01) — Sandoz Inc.
- Clindamycin Phosphate Injection
Clindamycin Phosphate, Injection, 150 mg/1 mL (NDC 25021-115-02) — Sagent Pharmaceuticals
- Amphetamine Aspartate Monohydrate, Amphetamine Sulfate, Dextroamphetamine Saccharate, Dextroamphetamine Sulfate Tablet
Amphetamine Aspartate Monohydrate, Amphetamine Sulfate, Dextroamphetamine Saccharate, Dextroamphetamine Sulfate, Tablet, 7.5 mg; 7.5 mg; 7.5 mg; 7.5 mg (NDC 0185-2099-01) — Sandoz Inc.
- Amphetamine Aspartate Monohydrate, Amphetamine Sulfate, Dextroamphetamine Saccharate, Dextroamphetamine Sulfate Tablet
Amphetamine Aspartate Monohydrate, Amphetamine Sulfate, Dextroamphetamine Saccharate, Dextroamphetamine Sulfate, Tablet, 2.5 mg; 2.5 mg; 2.5 mg; 2.5 mg (NDC 0185-0842-01) — Sandoz Inc.
Showing 12 of 22. Search the rest in openFDA.
Drug approvalsCovers FDA's Fri, Oct 2 (a week ago)12
- DOXERCALCIFEROL
DOXERCALCIFEROL — HIKMA
- EXENATIDE SYNTHETIC
EXENATIDE SYNTHETIC — AMNEAL
- CLOZAPINE
CLOZAPINE — MYLAN
- CLOZAPINE
CLOZAPINE — ACCORD HLTHCARE
- JAYPIRCA
PIRTOBRUTINIB — LOXO ONCOL
- METHYLPHENIDATE HYDROCHLORIDE
METHYLPHENIDATE HYDROCHLORIDE — ALVOGEN
- CYPROHEPTADINE HYDROCHLORIDE
CYPROHEPTADINE HYDROCHLORIDE — QUAGEN
- DIVALPROEX SODIUM
DIVALPROEX SODIUM — COSETTE PHARMS NC
- PERAMPANEL
PERAMPANEL — AUROBINDO PHARMA LTD
- CELECOXIB
CELECOXIB — UNICHEM
- FOSAPREPITANT DIMEGLUMINE
FOSAPREPITANT DIMEGLUMINE — BAXTER HLTHCARE CORP
- EXCEDRIN (MIGRAINE RELIEF)
ACETAMINOPHEN, ASPIRIN, CAFFEINE — HALEON US HOLDINGS
Device clearancesCovers FDA's Fri, Sep 25 (two weeks ago)21
- syngo.CT Brain Quantification
Siemens Medical Solutions USA, Inc.
- Braun Aura 9 (6042)
Cyden Limited
- REBOHIL (BGM-1, BGM-2, BGM-3, BGM-4, BGM-5)
Hyundai Bioland Co., Ltd.
- Xpert Respiratory Panel
Cepheid
- Profoject Safety Sliding Blood Collection Set
CMT Health PTE., Ltd.
- Arthrex Beaming System
Arthrex, Inc.
- DistaSense(TM) (v1)
Life Detection Technologies
- UNIDRIVE SIII System; HOPKINS Telescope 0º (26205AMA) Operating Sheath (26205CD) Obturator (26205OC) Shaver Blade (2620…
Karl Storz SE & CO. KG
- S-Patch CardioAI
Wellysis Corp.
- CapsoView (CVV); CapsoCloud (CLD)
CapsoVision, Inc.
- Altis Full Face Mask
Respironics, Inc.
- TumorSight Risk
SimBioSys, Inc.
Showing 12 of 21. Search the rest in openFDA.
How the FDA Daily Is WrittenSources, dates and what gets flagged
Every issue is written from FDA's public data (openFDA) and nothing else: the counts, names, firms and reasons are FDA's own. openFDA posts each kind of record on its own delay, so each section covers one FDA date and says which. Shortages cover yesterday; approvals, drug recalls, device recalls and food and supplement recalls cover a week ago; device clearances and label changes cover two weeks ago. Every FDA date appears in exactly one issue. Items that touch the categories MedGrid works in, such as GLP-1s, hormones, injectables, peptides, compounded products and aesthetic devices, are marked and listed first.
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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.