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

3151–3175 of 8589

SevereFDA (Drugs)·D-0238-2019·2018-11-14
Qualgen Testosterone and Anastrozole Pellets Recalled for Sterility Concerns
Qualgen, LLC is recalling Testosterone 200 mg/Anastrozole 20 mg pellets due to a lack of assurance of sterility. The recall affects specific vial sizes distributed nationwide.
Product
Testosterone 200 mg/Anastrozole 20 mg pellet, 1 count (NDC 69761-222-01), 6 count (NDC 69761-222-06), 12 count (NDC 69761-222-12), and 30 count (NDC 69761-222-30) vials, Rx Only, Qualgen, Edmond, OK 73013
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0237-2019·2018-11-14
Qualgen Recalls Testosterone Pellets Due to Sterility Concerns
Qualgen, LLC is recalling specific lots of Testosterone 87.5mg pellets nationwide due to a lack of assurance of sterility.
Product
Testosterone 87.5mg pellet, 1 count (NDC 69761-187-01), 6 count (NDC 69761-187-06), 12 count (NDC 69761-187-12), and 30 count (NDC 69761-187-30) vials, Rx Only Qualgen, LLC, Edmond, OK 73013
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0208-2019·2018-11-07
Pharm D Solutions Recalls Trimix T-106 Due to Sterility Concerns
Pharm D Solutions is recalling specific lots of Trimix T-106 aqueous solution because the company cannot ensure the product is sterile.
Product
Trimix T-106 30PA-1PH-25A Aqueous Solution Pharm D Solutions, Houston, Texas --- NDC 69699-1339-05
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0214-2019·2018-11-07
Pharm D Solutions Recalls Testosterone Cypionate/Proprinate Injectable Due to Sterility Concerns
Pharm D Solutions is recalling specific lots of Testosterone Cypionate/Proprinate 200 mg/10 mg/1 mL 30 mL Injectable because of a lack of assurance of sterility.
Product
Testosterone Cypionate/Proprinate 200 mg/10 mg/1 mL 30 mL Injectable, Pharm D Solutions, Houston, Texas --- NDC 69699-1745-30
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0172-2019·2018-11-07
Pharm D Solutions Recalls Phosphate Buffer Solution Due to Sterility Concerns
Pharm D Solutions is recalling specific lots of Phosphate Buffer Solution 0.05 m Aqueous Solution because the company cannot assure the product's sterility.
Product
Phosphate Buffer Solution 0.05 m Aqueous Solution, Pharm D Solutions, Houston, Texas --- NDC 69699-0912-20
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0187-2019·2018-11-07
Pharm D Solutions Recalls 0.9% Sodium Chloride Injection Bags Due to Sterility Concerns
Pharm D Solutions is recalling 50 mL bags of 0.9% Sodium Chloride for Injection because the company cannot ensure the product is sterile.
Product
0.9% Sodium Chloride for Injection, 50 mL bags, Pharm D Solutions, Houston, Texas --- NDC 69699-1426-10
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0194-2019·2018-11-07
Pharm D Solutions Recalls Trimix Injectable Due to Sterility Concerns
Pharm D Solutions is recalling specific lots of Trimix QM10 Injectable because the company cannot ensure the product is sterile.
Product
Trimix QM10 Papaverine 30 mg/Phentolamine 4 mg/Atropine 1 mg/PGE 150 mcg/mL Injectable, Pharm D Solutions, Houston, Texas --- NDC 69699-1352-05
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0153-2019·2018-11-07
Pharm D Solutions Recalls Glutamine Solution Due to Sterility Concerns
Pharm D Solutions is recalling Glutamine 10 mg/mL Solution because the product lacks assurance of sterility. The recall covers specific lots distributed nationwide.
Product
Glutamine 10 mg/mL Solution, Pharm D Solutions, Houston, Texas ---- NDC 69699-1439-59
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0191-2019·2018-11-07
Pharm D Solutions Recalls Tri-Mix Injectable Due to Sterility Concerns
Pharm D Solutions is recalling 609 vials of Tri-Mix Injectable due to a lack of assurance of sterility. The product was distributed nationwide.
Product
Tri-Mix Papaverine/Phentolamine/Alprostadil 150 mg/5 mg/50 mcg a) Injectable NDC 69699-1332-05 b) (LYO) Powder NDC 69699-1332-05, Pharm D Solutions, Houston, Texas
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0195-2019·2018-11-07
Pharm D Solutions Recalls Trimix T 101 Injectable Due to Sterility Concerns
Pharm D Solutions is recalling Trimix T 101 Injectable due to a lack of assurance of sterility. The recall covers a specific lot distributed nationwide.
Product
Trimix T 101 Alprostadil/Papverine/Phentolamine 5.9 mcg/17.65 mg/0.59 mcg per mL Injectable, Pharm D Solutions, Houston, Texas --- NDC 69699-1336-05
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0193-2019·2018-11-07
Pharm D Solutions Recalls Trimix Injectable Due to Sterility Concerns
Pharm D Solutions is recalling Trimix BM3 Papaverine 30 mg/Phentolamine 1 mg Injectable because the agency could not ensure the product was sterile.
Product
Trimix BM3 Papaverine 30 mg/Phentolamine 1 mg Injectable, Pharm D Solutions, Houston, Texas --- NDC 69699-1354-03
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0131-2019·2018-11-07
Avella Recalls Morphine Bags Due to Sterility Assurance Concerns
Avella of Deer Valley is recalling 1,360 bags of Morphine in NS due to a lack of assurance of sterility. The product was distributed nationwide.
Product
Morphine (1 mg/mL) in NS 100 mL Bag, Rx only, Advanced Pharma, Inc. d/b/a Avella of Houston, and Avella of Deer Valley, Inc. #38
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0152-2019·2018-11-07
Pharm D Solutions Recalls Epinephrine Injectable Due to Sterility Concerns
Pharm D Solutions is recalling 945 syringes of Epinephrine 1 mg/1 mL injectable solution nationwide due to a lack of assurance of sterility.
Product
Epinepherine 1 mg/1 mL 3 mL Injectable Pharm D Solutions, Houston, Texas ---- NDC 69699-0109-03
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0186-2019·2018-11-07
FDA Recalls Slenderella Compound Injectable Due to Sterility Concerns
Pharm D Solutions is recalling Slenderella Compound Injectable because the product lacks assurance of sterility.
Product
Slenderella Compound Injectable, Pharm D Solutions, Houston, Texas --- NDC 69699-1617-30
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0138-2019·2018-11-07
Pharm D Solutions Recalls Ascorbic Acid Solution Due to Sterility Concerns
Pharm D Solutions is recalling Ascorbic Acid 500 mg/mL Solution due to a lack of assurance of sterility. The recall affects nationwide distribution.
Product
Ascorbic Acid 500 mg/mL Solution Pharm D Solutions, Houston, Texas --- NDC 69699-1502-50
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0206-2019·2018-11-07
Pharm D Solutions Recalls Trimix Aqueous Solution Due to Sterility Concerns
Pharm D Solutions is recalling specific lots of Trimix aqueous solution because the agency could not ensure the product was sterile.
Product
Trimix ST9D 30PA-2PH-150A Aqueous Solution Pharm D Solutions, Houston, Texas --- NDC 69699-1311-03
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0213-2019·2018-11-07
Pharm D Solutions Recalls Testosterone Injectable Due to Sterility Concerns
Pharm D Solutions is recalling Testosterone in Grapeseed Oil Injectable because the product lacks assurance of sterility. The recall covers multiple vial sizes distributed nationwide.
Product
Testosterone in Grapeseed Oil 200 mg/mL, a) 4 mL, b) 5 mL, c) 10 mL and d) 30 mL Injectable, Pharm D Solutions, Houston, Texas NDC 69699-1702-05
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0207-2019·2018-11-07
Pharm D Solutions Recalls Trimix T-101 Injection Due to Sterility Concerns
Pharm D Solutions is recalling Trimix T-101 injection because the product may lack assurance of sterility.
Product
Trimix T-101 Alprostadil/Phapaverine/Phentolamine 5.9 mcg/17.65 mg/Phentolamine 0.59 mcg per mL Pharm D Solutions, Houston, Texas --- NDC 69699-1366-05
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0144-2019·2018-11-07
Pharm D Solutions Recalls Bi-Mix Injectable Due to Sterility Concerns
Pharm D Solutions is recalling 29 vials of Bi-Mix (Papaverine/Phentolamine) injectable and powder nationwide due to a lack of assurance of sterility.
Product
Bi-Mix (Papaverine/Phentolamine 150 mg/5 mg) a) Injectable NDC 69699-1760-15; b) (LYO) Powder NDC 69699-1760-15, Pharm D Solutions, Houston, Texas
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0204-2019·2018-11-07
Pharm D Solutions Recalls Trimix ST-9B Due to Sterility Concerns
Pharm D Solutions is recalling specific lots of Trimix ST-9B aqueous solution because the company cannot guarantee the product's sterility.
Product
Trimix ST-9B 30 PA-2PH-100A Aqueous Solution Pharm D Solutions, Houston, Texas --- NDC 69699-1344-05
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0197-2019·2018-11-07
Pharm D Solutions Recalls Trimix Injectable Due to Sterility Concerns
Pharm D Solutions is recalling specific lots of Trimix Injectable because the agency could not ensure the product was sterile.
Product
Trimix Alprostadil/ Phentolamine/Papavarin 40 mcg/1 mg/30 mg 10 mL Injectable, Pharm D Solutions, Houston, Texas --- NDC 69699-1330-05
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0180-2019·2018-11-07
Pharm D Solutions Recalls Sermorelin/GHRP-2 Powder Due to Sterility Concerns
Pharm D Solutions is recalling 409 vials of Sermorelin/GHRP-2 powder because the company cannot ensure the product is sterile.
Product
Sermorelin/GHRP-2 6 mg/6 mg Powder, Pharm D Solutions, Houston, Texas --- NDC 69699-1727-10
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0169-2019·2018-11-07
Pharm D Solutions Recalls Oxytocin IV Bags Due to Sterility Concerns
Pharm D Solutions is recalling 264 vials of Oxytocin 30 unit in LR 500 mL IV bags nationwide due to a lack of assurance of sterility.
Product
Oxytocin 30 unit in LR 500 mL 0.06 units/mL IV,Pharm D Solutions, Houston, Texas --- NDC 69699-1203-50
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0160-2019·2018-11-07
Pharm D Solutions Recalls HCG Injectable Due to Sterility Concerns
Pharm D Solutions is recalling 881 vials of HCG Lyopholized 1200 IU Injectable nationwide due to a lack of assurance of sterility.
Product
HCG Lyopholized 1200 IU Injectable, Pharm D Solutions, Houston, Texas ---- NDC 69699-1743-12
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0133-2019·2018-11-07
Avella Recalls Hydromorphone Bags Due to Sterility Assurance Concerns
Avella of Deer Valley, Inc. is recalling 360 bags of Hydromorphone in NS due to a lack of assurance of sterility. The product was distributed nationwide.
Product
Hydromorphone (0.2 mg/mL) in NS 100 mL Bag, Rx only, Advanced Pharma, Inc. d/b/a Avella of Houston, and Avella of Deer Valley, Inc. #38
Category
Drug
Distribution
Distributed nationwide

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3151–3175 of 8589