Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

6626–6650 of 113877

HighFDA (Drugs)·D-0009-2026·2025-10-15
Chlorpromazine 25 mg fifty count packs recalled over nitrosamine impurity
Major Pharmaceuticals is recalling 2,064 fifty-tablet blister packs of Chlorpromazine Hydrochloride Tablets USP 25 mg because a nitrosamine impurity exceeded the recommended intake limit.
Product
Major ChlorproMAZINE Hydrochloride Tablets, USP, 25 mg, 50 Tablets (5x10) blister package, Rx Only, Packaged and Distributed by Major Pharmaceuticals, Indianapolis, IN 46268, USA, NDC 0904-7130-06, UPC (01)00309047130061
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0078-2026·2025-10-15
Pentosan for injection recalled across all lots over sterility assurance
GenoGenix is recalling Pentosan for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
Product
Pentosan for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0073-2026·2025-10-15
EDTA for injection recalled across all lots over sterility assurance
GenoGenix is recalling EDTA for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
Product
EDTA for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0047-2026·2025-10-15
B-Complex injection recalled across all lots over lack of sterility assurance
GenoGenix is recalling B-Complex for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
Product
B-Complex for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692. B-Complex with B12 also labeled as manufactured for Synergy Wellness.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0046-2026·2025-10-15
Bacteriostatic water for injection recalled over lack of sterility assurance
GenoGenix is recalling Bacteriostatic Water for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
Product
Bacteriostatic Water for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692. Also labeled as manufactured for CELIA Health, Extension Health and Medical Health Institute
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0080-2026·2025-10-15
Buffered reconstitution solution recalled across all lots over sterility assurance
GenoGenix is recalling pH Buffered Reconstitution Solution for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
Product
pH Buffered Reconstitution Solution for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692. Also labeled as manufactured for Medical Health Institute (MHI), 10mL.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0092-2026·2025-10-15
Tirzepatide injection recalled from two lots over lack of sterility assurance
GenoGenix is recalling Tirzepatide 60mg/10 mL for Injection from two lots for lack of assurance of sterility.
Product
Tirzepatide, 60mg/10 mL for Injection, 10mL vial lyophilized, all presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692. Also labeled as manufactured for Extension Health and Synergy Wellness 60mg, 10mL vial lyophilized.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0052-2026·2025-10-15
Glutathione magnesium injection recalled across all lots over sterility assurance
GenoGenix is recalling Glutathione Magnesium for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
Product
Glutathione Magnesium for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692. Also labeled as manufactured for CELIA Health.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0054-2026·2025-10-15
Glycine for injection recalled across all lots over sterility assurance
GenoGenix is recalling Glycine for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
Product
Glycine for Injection, all strengths and presentations, GenoGenix LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0128-2026·2025-10-15
Nasal feeding tubes recalled because distal tips may detach too easily
Applied Medical Technology is recalling 390 NutraGlide nasal feeding tubes whose distal tips may detach at lower than expected forces.
Product
NutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 F - 6 F x 90, REF E NRT-05090-I The NutraGlide Nasal Feeding Tube is a feeding tube placed through the nose and ending in the stomach or intestine used for the administration of nutrition, fluids, and medications in neonatal
Category
Medical Device
Distribution
2 states
HighFDA (Drugs)·D-0074-2026·2025-10-15
Exosome reconstitution solution recalled across all lots over sterility assurance
GenoGenix is recalling Elite Stack MSC Exosome Reconstitution Solution for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
Product
Elite Stack MSC Exosome Reconstitution Solution for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692. Also labeled as manufactured for Extension Health, a) 22 billion per vial, 8mL of solution in 10mL vial, b) 44 billio
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0090-2026·2025-10-15
Sermorelin lyophilized powder recalled from one lot over sterility assurance
GenoGenix is recalling Sermorelin lyophilized powder for reconstitution, 10mg in a 10 mL multi-dose vial, from a single lot for lack of assurance of sterility.
Product
Sermorelin Lyophilized powder for reconstitution, 10mg, Vial capacity 10 mL Multi-Dose, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0130-2026·2025-10-15
Larger nasal feeding tubes recalled because distal tips may detach
Applied Medical Technology is recalling 200 NutraGlide 5 F - 8 F nasal feeding tubes whose distal tips may detach at lower than expected forces.
Product
NutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 F - 8 F x 90, REF E NRT-06090-I The NutraGlide Nasal Feeding Tube is a feeding tube placed through the nose and ending in the stomach or intestine used for the administration of nutrition, fluids, and medications in neonatal
Category
Medical Device
Distribution
2 states
HighFDA (Devices)·Z-0040-2026·2025-10-15
Scleral reinforcement matrix recalled after complaints of early patch exposure
CorNeat Vision is recalling 180 EverPatch+ units after reviewed complaints identified that conjunctival wound dehiscence may result in early exposure of the surgical patch.
Product
EverPatch+, REF: 1044002, Permanent Scleral Reinforcement Matrix 1x5.0mm x 8.5 mm Shield/1 x 5.0mm x 6.5 mm Rectangle, STERILE VH202
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0087-2026·2025-10-15
Thymosin Beta-4 injection recalled from one lot over sterility assurance
GenoGenix is recalling Thymosin Beta-4 (TB4) for Injection, 15mg, in all presentations from a single lot for lack of assurance of sterility.
Product
Thymosin Beta-4 (TB4) for Injection, 15mg, all presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0057-2026·2025-10-15
L-Carnitine for injection recalled across all lots over sterility assurance
GenoGenix is recalling L-Carnitine for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
Product
L-Carnitine for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0045-2026·2025-10-15
Pyridoxine B6 injection recalled across all lots over sterility assurance
GenoGenix is recalling B6 (Pyridoxine HCl) for Injections in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
Product
B6 (Pyridoxine HCl) for Injections, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692. Also labeled as manufactured for Synergy Wellness
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0063-2026·2025-10-15
Methylene blue injection recalled across all lots for sterility assurance concerns
GenoGenix is recalling Methylene Blue for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
Product
Methylene Blue for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·H-0021-2026·2025-10-15
Whey protein powder recalled for undeclared milk allergen across many lots
New Spirit Naturals is recalling 37 containers of Ultra Whey Protein Powder because the product contains undeclared milk.
Product
Ultra Whey Protein Powder; 1.4 lbs and 1.4 lbs. Chocolate flavor UPC: NA
Category
Food
Distribution
0 states
HighFDA (Drugs)·D-0048-2026·2025-10-15
Biotin for injection recalled across all lots over sterility assurance
GenoGenix is recalling Biotin for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
Product
Biotin for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·H-0130-2026·2025-10-15
Mint flavored chewable tablets recalled for undeclared Yellow 5 color additive
Eden's Elixirs is recalling 10,000 Eskay Brands mint flavored chewable tablets distributed in Texas because Yellow #5 is not declared.
Product
Eskay Brands Mint flavored tablets. 40mg 7OH/550mg Tablet- Eskay Brands-Mint, Chewable tablet, no shelf-life. Dosage: 2 doses per tablet. 10,000 or less per bulk bag. Bulk package and is not sold directly to consumer.
Category
Food
Distribution
1 state
ModerateFDA (Devices)·Z-0114-2026·2025-10-15
Epidural basic trays recalled over catheter connector lid position defect
B. Braun is recalling PERIFIX FX Continuous Epidural Anesthesia Trays, product code CE17TBFC, because the lid of the catheter connector may be in the incorrect position.
Product
PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. x 3-1/2 in. (9cm) Tuohy Epidural Needle - Winged and PERIFIX FX Springwound Catheter - 19 Ga. Closed Tip. Product Code: CE17TBFC. Product description: CE17TBFC EPIDURAL BASIC TRAY 17G TOUHY.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0119-2026·2025-10-15
Epidural anesthesia trays recalled over catheter connector lid position defect
B. Braun is recalling 21,270 PERIFIX FX Continuous Epidural Anesthesia Trays because the lid of the catheter connector may be in the incorrect position.
Product
PERIFIX FX Continuous Epidural Anesthesia Tray, PERIFIX 17 Ga. x 3-1/2 in. (8.9 cm) Tuohy Epidural Needle - Winged and 19 Ga. Closed tip PERIFIX FX Springwound Epidural Catheter. Product Code: CE17TKFCS. Product Description: CE17TKFCS CONT EPID TRAY W/17G TUOHY-LF.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0121-2026·2025-10-15
Continuous epidural anesthesia sets recalled over catheter connector lid position
B. Braun is recalling PERIFIX FX Continuous Epidural Anesthesia Sets, product code CE17TFC, because the lid of the catheter connector may be in the incorrect position.
Product
PERIFIX FX Continuous Epidural Anesthesia Set, PERIFIX Tuohy Epidural Needle - 17 Ga. x 3-1/2 in. (8.9 cm) - Winged, PERIFIX FX Springwound Epidural Catheter - 19 Ga. Closed tip. Product Code: CE17TFC. Product Description: CE17TFC CONTINUOUS EPID SET W/17G TUOHY.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0122-2026·2025-10-15
ESPOCAN spinal epidural trays recalled over catheter connector lid position
B. Braun is recalling 10,130 ESPOCAN Combined Spinal and Epidural Anesthesia Trays because the lid of the catheter connector may be in the incorrect position.
Product
ESPOCAN Combined Spinal and Epidural Anesthesia Tray, ESPOCAN 17 Ga. x 3-1/2 in. (8.9 cm) Tuohy Epidural Needle, PENCAN 25 Ga. x 5 in. (12.7 cm) Spinal Needle with Marking and Centering Sleeve, and 19 Ga. Closed Tip PERIFIX FX Springwound Epidural Catheter. Product Code: ES1725KF
Category
Medical Device
Distribution
Distributed nationwide

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6626–6650 of 113877