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 the agency’s own highest classification or reported deaths or serious injuries, 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

33826–33850 of 39756

SevereFDA (Devices)·Z-2179-2013·2013-09-18
Monoject Flush Syringes Recalled for Potential Non-Sterile Water Contamination
FDA is recalling Monoject 0.9% Sodium Chloride Flush Syringes because they may contain non-sterile water. The products are distributed in the US and Bermuda.
Product
Monoject 0.9% Sodium Chloride Flush Syringe, 12 mL Syringe with 3 mL Fill Product ID: 8881570123 Product Usage: Both 0.9% Sodium Chloride Flush syringes and 10U/mL or 100U/mL Heparin Lock Flush syringes are sterile, single-use products which are intended for use in flushing…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-967-2013·2013-09-18
Beacon Hill Medical Pharmacy Recalls Hydrogen Peroxide Injectable Due to Sterility Concerns
Beacon Hill Medical Pharmacy is recalling Hydrogen Peroxide 3% Injectable because FDA inspections raised concerns about quality control and sterility assurance.
Product
HYDROGEN PEROXIDE 3% INJECTABLE, all presentations, FOR INTRAVENO and SQ USE ONLY, STERILE, RX ONLY, Compounded by Beacon Hill Medical Pharmacy PC, dba Rxtra Solutions, Southfield, MI
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·13V455000·2013-09-18
NOV Rolligon Recalls Trailers Due to Missing Suspension Weld
NOV Rolligon is recalling specific 2011-2012 trailers because a missing weld on the rear suspension could cause the trailer to pull to one side or shift load, increasing crash risk.
Product
ROLLIGON — ROLLIGON MT-1060, HT-180, MT-1060-HR, HT-270
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1018-2013·2013-09-18
Beacon Hill Medical Pharmacy Recalls Manganese Sulfate Injectable Due to Sterility Concerns
Beacon Hill Medical Pharmacy is recalling Manganese Sulfate 0.1 mg/mL Injectable due to FDA inspectional findings regarding sterility assurance.
Product
MANGANESE SULFATE 0.1 MG/ML INJECTABLE, all configurations, FOR INTRAVENO AND SQ USE ONLY, STERILE, RX ONLY, Compounded by Beacon Hill Medical Pharmacy PC, dba Rxtra Solutions, Southfield, MI
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-949-2013·2013-09-18
Beacon Hill Medical Pharmacy Recalls Dextrose PF 50% Injectable Due to Sterility Concerns
Beacon Hill Medical Pharmacy is recalling Dextrose PF 50% Injectable because FDA inspections raised concerns about quality control and sterility assurance.
Product
DEXTROSE PF 50% INJECTABLE, all presentations, FOR INTRAVENO AND SQ USE ONLY, STERILE, RX ONLY, Compounded by Beacon Hill Medical Pharmacy PC, dba Rxtra Solutions, Southfield, MI
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1005-2013·2013-09-18
Beacon Hill Medical Pharmacy Recalls TRI-MIX Injection Due to Sterility Concerns
Beacon Hill Medical Pharmacy is recalling TRI-MIX injection solutions because FDA inspectional findings raised concerns about sterility assurance and quality control.
Product
TRI-MIX 10 MCG/30 MG/1 MG/ML INJ SOLN and TRI-MIX 30 MCG/15 MG/2 MG/ML INJ SOLN, all configuration, FOR INTRAVENO AND SQ USE ONLY, STERILE, RX ONLY, Compounded by Beacon Hill Medical Pharmacy PC, dba Rxtra Solutions, Southfield, MI
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-972-2013·2013-09-18
Beacon Hill Medical Pharmacy Recalls L-Tryptophan Injectable Due to Sterility Concerns
Beacon Hill Medical Pharmacy is recalling L-Tryptophan 300 mg/mL injectable due to FDA inspectional findings regarding sterility assurance.
Product
L-TRYPTOPHAN 300 MG/ML INJECTABLE, all presentations, FOR INTRAVENO and SQ USE ONLY, STERILE, RX ONLY, Compounded by Beacon Hill Medical Pharmacy PC, dba Rxtra Solutions, Southfield, MI
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-989-2013·2013-09-18
Beacon Hill Medical Pharmacy Recalls Potassium Chloride Injectable Due to Sterility Concerns
Beacon Hill Medical Pharmacy is recalling Potassium Chloride 2 mEq/mL Injectable because FDA inspectional findings raised concerns about sterility assurance and quality control procedures.
Product
POTASSIUM CHLORIDE 2 MEQ/ML INJECTABLE, all presentations, FOR INTRAVENO AND SQ USE ONLY, STERILE, RX ONLY, Compounded by Beacon Hill Medical Pharmacy PC, dba Rxtra Solutions, Southfield, MI
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-973-2013·2013-09-18
Beacon Hill Medical Pharmacy Recalls Lidocaine Injectable Due to Sterility Concerns
Beacon Hill Medical Pharmacy is recalling Lidocaine MDV and Lidocaine PF injectables because FDA inspectional findings raised concerns about quality control procedures that impacted sterility assurance.
Product
LIDOCAINE MDV 1% INJECTABLE, LIDOCAINE MDV 20 MG/ML INJECTABLE and Lidocaine PF 20 MG/ML INJECTABLE, all presentations, FOR INTRAVENO and SQ USE ONLY, STERILE, RX ONLY, Compounded by Beacon Hill Medical Pharmacy PC, dba Rxtra Solutions, Southfield, MI
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-987-2013·2013-09-18
Beacon Hill Medical Pharmacy Recalls Parabens Water for Injection Due to Sterility Concerns
Beacon Hill Medical Pharmacy is recalling all presentations of Parabens Water for Injection because FDA inspectional findings raised concerns about quality control procedures impacting sterility assurance.
Product
PARABEN WATER FOR INJECTION, all presentations, FOR INTRAVENO AND SQ USE ONLY, STERILE, RX ONLY, Compounded by Beacon Hill Medical Pharmacy PC, dba Rxtra Solutions, Southfield, MI
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1032-2013·2013-09-18
Wellness Pharmacy Recalls Methyl B12 Vials Due to Sterility Concerns
Wellness Pharmacy is recalling Methyl B12 1 mg/mL single-use vials because laboratory results indicated microbial contamination and the FDA questioned the reliability of the testing.
Product
Methyl B12 1 mg/mL P.F., Single-Use Vial, a) 1 mL, b) 10 mL, WELLNESS PHARMACY, 1-800-227-2627
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1008-2013·2013-09-18
FDA Recalls Triptropin Plus Injectable Due to Sterility Assurance Concerns
Beacon Hill Medical Pharmacy is recalling Triptropin Plus Injectable because FDA inspections raised concerns about quality control procedures that impacted sterility assurance.
Product
TRIPTROPIN PLUS INJECTABLE, all configurations, FOR INTRAVENO AND SQ USE ONLY, STERILE, RX ONLY, Compounded by Beacon Hill Medical Pharmacy PC, dba Rxtra Solutions, Southfield, MI
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-998-2013·2013-09-18
Sodium Bicarbonate Injectable Recalled for Sterility Assurance Concerns
Beacon Hill Medical Pharmacy is recalling Sodium Bicarbonate PF 8.4% Injectable due to FDA inspectional findings regarding quality control and sterility assurance.
Product
SODIUM BICARBONATE PF 8.4% INJECTABLE, all presentations, FOR INTRAVENO AND SQ USE ONLY, STERILE, RX ONLY, Compounded by Beacon Hill Medical Pharmacy PC, dba Rxtra Solutions, Southfield, MI
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1002-2013·2013-09-18
FDA Recalls Testosterone Injectable Due to Sterility Assurance Concerns
Beacon Hill Medical Pharmacy is recalling Testosterone Hypoallergenic and Testosterone Aqueous injectables due to FDA inspectional findings regarding sterility assurance.
Product
TESTOSTERONE HYPOALLERGENIC 200 MG/ML INJECTABLE and TESTOSTERONE AQUEOUS 100 MG/ML INJECTABLE, all presentations, FOR INTRAVENO AND SQ USE ONLY, STERILE, RX ONLY, Compounded by Beacon Hill Medical Pharmacy PC, dba Rxtra Solutions, Southfield, MI
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-995-2013·2013-09-18
Beacon Hill Medical Pharmacy Recalls Quad Amino Blend Injectable Due to Sterility Concerns
Beacon Hill Medical Pharmacy is recalling Quad Amino Blend 150/75/150/75 mg/mL Injectable due to FDA inspectional findings regarding sterility assurance.
Product
QUAD AMINO BLEND 150/75/150/75 MG/ML INJECTABLE, all presentations, FOR INTRAVENO AND SQ USE ONLY, STERILE, RX ONLY, Compounded by Beacon Hill Medical Pharmacy PC, dba Rxtra Solutions, Southfield, MI
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1031-2013·2013-09-18
Wellness Pharmacy Recalls Magnesium Sulfate Vials Due to Sterility Concerns
Wellness Pharmacy is recalling 590 vials of Magnesium Sulfate Hepta 50% PF due to laboratory results indicating microbial contamination and concerns about the reliability of testing.
Product
Magnesium Sulfate Hepta 50% PF, Single Use Vial, a) 2 mL, b) 10 mL, WELLNESS PHARMACY, 1-800-227-2627
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-976-2013·2013-09-18
Beacon Hill Medical Pharmacy Recalls Magnesium Chloride Injectable Due to Sterility Concerns
Beacon Hill Medical Pharmacy is recalling all presentations of Magnesium Chloride Hexahydrate 20% Injectable due to FDA inspectional findings regarding quality control and sterility assurance.
Product
MAGNESIUM CHLORIDE HEXAHYDRATE 20% INJECTABLE, all presentations, FOR INTRAVENO and SQ USE ONLY, STERILE, RX ONLY, Compounded by Beacon Hill Medical Pharmacy PC, dba Rxtra Solutions, Southfield, MI
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-954-2013·2013-09-18
Beacon Hill Medical Pharmacy Recalls Estradiol Injection Due to Sterility Concerns
Beacon Hill Medical Pharmacy is recalling Estradiol Cypionate/Progesterone/Testosterone Cypionate injections due to FDA inspectional findings regarding sterility assurance.
Product
ESTRADIOL CYP/PROG/TEST CYP 0.5/10/10 MG/ML OIL INJ SOLN, all presentations, FOR INTRAVENO AND SQ USE ONLY, STERILE, RX ONLY, Compounded by Beacon Hill Medical Pharmacy PC, dba Rxtra Solutions, Southfield, MI
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2127-2013·2013-09-18
Siemens MicroscanrapID/S panels recalled for antimicrobial misreads
Siemens Healthcare Diagnostics is recalling MicroscanrapID/S panels due to confirmed false susceptible and intermediate results for imipenem and meropenum.
Product
MicroscanrapID/S panels NC3.11 Sold in Japan only. Product Usage: MicroScan¿ Synergies plus¿ Panels & MicroScan¿ Rapids plus (Negative) - For use in determining quantitative and/or qualitative antimicrobial agent susceptibility and/or identification for gram-negative…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2128-2013·2013-09-18
Siemens Microscan rapID/S panels recalled for false susceptibility results
Siemens Healthcare Diagnostics is recalling Microscan rapID/S panels due to confirmed false susceptibility and intermediate misreads for imipenem and meropenum.
Product
Microscan rapID/S panels NC3.12 Sold in Japan only. Product Usage: MicroScan¿ Synergies plus¿ Panels & MicroScan¿ Rapids plus (Negative) - For use in determining quantitative and/or qualitative antimicrobial agent susceptibility and/or identification for…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-957-2013·2013-09-18
Beacon Hill Medical Pharmacy Recalls Estriol Oil Injection Due to Sterility Concerns
Beacon Hill Medical Pharmacy is recalling Estriol 5 mg/mL oil injection solution because FDA inspections raised concerns about sterility assurance and quality control.
Product
ESTRIOL 5 MG/ML OIL INJ SOLN, all presentations, FOR INTRAVENO AND SQ USE ONLY, STERILE, RX ONLY, Compounded by Beacon Hill Medical Pharmacy PC, dba Rxtra Solutions, Southfield, MI
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-1879-2013·2013-09-18
Reaction Nutrition Recalls Immune Support Supplement for Undeclared Colostrum Allergen
Reaction Nutrition LLC is recalling 600 bottles of Clinical LIVE Immune Support capsules because they contain undeclared colostrum, a dairy allergen.
Product
Clinical LIVE Dietary Supplement Immune Support 694.325 mg 90 capsules Distributed by Reaction Nutrition, LLC., Carnegie, PA.
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·13V441000·2013-09-18
Spartan Motors Recalls 2011-2013 Transit Buses for Control Arm Fracture Risk
Spartan Motors is recalling 75 model year 2011-2013 Transit Bus Chassis Cab vehicles because front suspension control arms may fracture without warning, increasing crash risk.
Product
SPARTAN MOTORS — SPARTAN MOTORS TRANSIT BUS CHASSIS CAB
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2186-2013·2013-09-18
Monoject Heparin Lock Flush Syringes Recalled for Potential Non-Sterile Water
The FDA is recalling Monoject 100 Units/mL Heparin Lock Flush syringes because they may contain non-sterile water while labeled as saline or heparin.
Product
Monoject 100 Units/mL Heparin Lock Flush, 12 mL Syringe with 5 mL Fill Product ID: 8881590125 Product Usage: Both 0.9% Sodium Chloride Flush syringes and 10U/mL or 100U/mL Heparin Lock Flush syringes are sterile, single-use products which are intended for use in flushing…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-953-2013·2013-09-18
Beacon Hill Medical Pharmacy Recalls EDETATE DISODIUM INJECTABLE Due to Sterility Concerns
Beacon Hill Medical Pharmacy is recalling EDETATE DISODIUM 150 MG/ML INJECTABLE because FDA inspectional findings raised concerns about quality control procedures impacting sterility assurance.
Product
EDETATE DISODIUM 150 MG/ML INJECTABLE, all presentations, FOR INTRAVENO AND SQ USE ONLY, STERILE, RX ONLY, Compounded by Beacon Hill Medical Pharmacy PC, dba Rxtra Solutions, Southfield, MI
Category
Drug
Distribution
Distributed nationwide

How to read this listing

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33826–33850 of 39756