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

13851–13875 of 36679

SevereFDA (Drugs)·D-1428-2019·2019-07-03
Premier Pharmacy Labs Recalls Succinylcholine Chloride Syringes for Sterility Concerns
Premier Pharmacy Labs is recalling 1,721 syringes of Succinylcholine Chloride due to FDA findings of insufficient environmental controls and lack of sterility assurance.
Product
SUCCINYLcholine Chloride, 200mg/10mL (20mg/mL), 10mL Sterile Single Dose Syringe, Rx only, Premier Pharmacy Labs, 8265 Commercial Way, Weeki Wachee, FL 34613, NDC: 69623-239-16, barcode 9 69623 23916 0.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1411-2019·2019-07-03
Premier Pharmacy Labs Recalls Atropine Sulfate Injection Due to Sterility Concerns
Premier Pharmacy Labs is recalling 745 syringes of Atropine Sulfate Injection because FDA inspections found insufficient environmental controls that may compromise sterility.
Product
Atropine Sulfate PF INJ, 0.8 mg/2 mL (0.4 mg/mL), 2mL Single Dose Syringe, Rx only, Premier Pharmacy Labs, 8265 Commercial Way, Weeki Wachee, FL 34613, NDC: 69623-131-12, barcode 0 69623 13112 6.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1433-2019·2019-07-03
Pramipexole Dihydrochloride Tablets Recalled for GMP Deviations and Cross-Contamination Risk
American Health Packaging is recalling Pramipexole Dihydrochloride Tablets due to GMP deviations and a cleaning procedure failure that may have caused cross-contamination.
Product
Pramipexole Dihydrochloride Tablets, 0.5 mg, 30 Tablets (6 tablets per blister card), Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217 NDC Blister Card: 68084-974-95; NDC Carton: 68084-974-25
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1430-2019·2019-07-03
Diphenhydramine Liquid Recalled for Potential Microbial Contamination
H J Harkins Company is recalling Diphenhydramine HCL Liquid due to potential contamination with Burkholderia cepacia and Ralstonia pickettii.
Product
Diphenhydramine HCL Liquid, 12.5 mg/5 mL, 4 oz bottle, Manufactured by Torrent Pharma, Inc., Levittown, PA 19057, NDC 52959-0123-03.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1422-2019·2019-07-03
Premier Pharmacy Labs Recalls Neostigmine Methylsulfate Syringes for Sterility Concerns
Premier Pharmacy Labs is recalling Neostigmine Methylsulfate syringes nationwide due to FDA findings of insufficient environmental controls and lack of sterility assurance.
Product
Neostigmine Methylsulfate, 5mg/5mL (1mg/mL), 5mL Single Dose Syringe, Rx only, Premier Pharmacy Labs, 8265 Commercial Way, Weeki Wachee, FL 34613, NDC: 69623-234-15, barcode 5 69623 23415 0.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-1488-2019·2019-07-03
Parivar Dry Dates Recalled for High Sulfite Levels
Parivar brand Dry Dates are being recalled due to high levels of sulfites. The product was distributed to retail grocery stores in Florida, North Carolina, Georgia, and South Carolina.
Product
Parivar brand Dry Dates (Kharek) Net Wt.14 oz. (400 g) Product of India Batch No. 127/BHBI
Category
Food
Distribution
4 states
SevereFDA (Drugs)·D-1423-2019·2019-07-03
Premier Pharmacy Labs Recalls Orphenadrine Citrate Syringes Due to Sterility Concerns
Premier Pharmacy Labs is recalling 4,363 syringes of Orphenadrine Citrate Sterile Injectable Solution because FDA inspections found insufficient environmental controls that may compromise sterility.
Product
Orphenadrine Citrate Sterile Injectable Solution *Contains Sulfites*, 30mg/mL, 1mL Sterile Single-Use Syringe, Rx only, Premier Pharmacy Labs, 8265 Commercial Way, Weeki Wachee, FL 34613, NDC: 69623-104-10, barcode 7 69623 10410 5.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1888-2019·2019-07-03
Ethicon ENSEAL X1 Curved Jaw Tissue Sealer Recalled for Bleeding Risk
Ethicon Endo-Surgery Inc is recalling ENSEAL X1 Curved Jaw Tissue Sealers due to reported intraoperative bleeding.
Product
Ethicon ENSEAL X1 Curved Jaw Tissue Sealer 25cm Shaft PRODUCT CODE: NSLX125C
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·19V513000·2019-07-03
BMW Recalls Multiple Models for High Pressure Fuel Pump Defect
BMW is recalling specific 2019-2020 models because a high pressure fuel pump may not be properly attached, potentially causing a fuel leak and fire risk.
Product
BMW — BMW X5, M5, M850I, X7
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1413-2019·2019-07-03
Premier Pharmacy Labs Recalls Chlorpromazine Injection Due to Sterility Concerns
Premier Pharmacy Labs is recalling 824 vials of Chlorpromazine HCL Injection because an FDA inspection found insufficient environmental controls that may compromise sterility.
Product
ChlorproMAZINE HCL INJ, 25mg/mL, *Contains Sulfites*, 1mL in a 5mL Sterile SDV, Rx only, Premier Pharmacy Labs, 8265 Commercial Way, Weeki Wachee, FL 34613, NDC: 69623-122-28, barcode 7 69623 12228 4.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1415-2019·2019-07-03
Premier Pharmacy Labs Recalls Droperidol Syringes Due to Sterility Concerns
Premier Pharmacy Labs is recalling 2,315 syringes of Droperidol Injectable Sterile Solution because FDA inspections found insufficient environmental controls and lack of sterility assurance.
Product
Droperidol Injectable Sterile Solution, 0.625mg/mL, 1mL in a 3mL Sterile Single-Use Syringe, Rx only, Premier Pharmacy Labs, 8265 Commercial Way, Weeki Wachee, FL 34613, NDC: 69623-185-10, barcode 0 69623 18510 5.
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·19V508000·2019-07-02
Altec Recalls 2018-2019 Aerial Devices Due to Fastener Failure Risk
Altec is recalling 2018-2019 aerial devices because high-strength fasteners securing the pedestal to the turntable may fail, increasing the risk of injury or death.
Product
ALTEC — ALTEC AERIAL DEVICE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·19V510000·2019-07-02
Volvo Trucks Recalls 2019-2020 Models for Transmission Air Tank Strap Defect
Volvo Trucks is recalling 2019-2020 VAH, VHD, VNL, and VNR vehicles because over-tightened transmission air tank straps may deform and detach, creating a road hazard.
Product
VOLVO — VOLVO VNL, VHD, VNR, VAH
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·19V507000·2019-07-02
Mercedes-Benz and Freightliner Sprinter Vehicles Recalled for Rear Window Safety Glass
Daimler Vans USA is recalling 2018-2019 Mercedes-Benz and Freightliner Sprinter vans because rear side windows may be single-pane instead of laminated safety glass.
Product
MERCEDES-BENZ — MERCEDES-BENZ, FREIGHTLINER SPRINTER 1500, SPRINTER 2500, SPRINTER 4500, SPRINTER 3500
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·19V505000·2019-07-01
Forest River Recalls 2019 Rockport Trucks Due to Brake Controller Wiring
Forest River is recalling 2019 Rockport work trucks with optional trailer brake controllers due to improper wiring that may prevent trailer brakes from activating.
Product
FOREST RIVER — FOREST RIVER ROCKPORT
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·19V500000·2019-06-27
Honda and Acura Recall Vehicles for Air Bag Inflator Explosion Risk
Honda is recalling specific 2005-2015 Acura and Honda vehicles because driver frontal air bag inflators may explode due to propellant degradation, posing a risk of serious injury or death.
Product
HONDA — HONDA, ACURA CR-Z, RL, CR-V, RIDGELINE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·19V501000·2019-06-27
Honda Recalls Vehicles Due to Passenger Airbag Inflator Explosion Risk
Honda is recalling specific Acura and Honda models because the passenger frontal airbag inflator may explode, potentially causing serious injury or death.
Product
ACURA — ACURA, HONDA MDX, ACCORD, CIVIC, CR-V
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·19V498000·2019-06-27
2019 Ram Trucks Recalled for Diesel Fuel Line Leak Fire Risk
Chrysler is recalling 2019 Ram 2500, 3500, 4500, and 5500 diesel trucks because fuel lines may leak, increasing the risk of a fire.
Product
RAM — RAM 5500, 4500, 3500, 2500
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·19152·2019-06-27
Apple Recalls 15-Inch MacBook Pro Laptops Due to Fire Hazard
Apple is recalling about 432,000 15-inch MacBook Pro laptops because their batteries can overheat, posing a fire hazard.
Product
15-inch MacBook Pro laptop computers
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·19V496000·2019-06-27
Mazda Recalls 2016 MX-5 Vehicles for Detaching Skid Plate
Mazda is recalling 2016 MX-5 vehicles because the skid plate and metal bracket may detach, creating a road hazard and increasing crash risk.
Product
MAZDA — MAZDA MX-5
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·19V499000·2019-06-27
Honda and Acura Recall Vehicles for Air Bag Inflator Defect
Honda is recalling specific Acura and Honda models because driver frontal air bag inflators may explode, posing a risk of serious injury or death.
Product
HONDA — HONDA, ACURA ACCORD, CIVIC, CR-V, ELEMENT
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·19V502000·2019-06-27
Honda Recalls Vehicles for Passenger Air Bag Inflator Explosion Risk
Honda is recalling specific 2006-2015 models because the passenger frontal air bag inflator may explode due to propellant degradation, posing a risk of serious injury or death.
Product
HONDA — HONDA, ACURA CR-V, ACCORD, TSX, PILOT
Category
Vehicle
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1759-2019·2019-06-26
Teleflex Recalls Sheridan LTS Tracheal Tubes Due to Connector Disconnection
Teleflex Medical is voluntarily recalling specific lots of Sheridan LTS tracheal tubes because the 15 mm connector may disconnect from the tube.
Product
Hudson RCI Sheridan LTS, Product Code 5-11112 Product Usage: Tracheal tube/airway management
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Food)·F-1461-2019·2019-06-26
Maine Wild Blueberry Company Recalls Frozen Wild Blueberries Due to Listeria
Maine Wild Blueberry Company is recalling 30-lb cases of frozen wild blueberries after internal sampling detected Listeria monocytogenes. The product was not distributed to consumers.
Product
30 Lbs IQF Wild Blueberries, Keep Frozen -10*C
Category
Food
Distribution
1 state
CriticalFDA (Devices)·Z-1757-2019·2019-06-26
Cook Inc. Recalls Advance Enforcer 35 Focal Force PTA Balloon Catheters
Cook Inc. is recalling 131 Advance Enforcer 35 Focal Force PTA Balloon Catheters because multiple complaints reported the balloons bursting below their rated pressure.
Product
Advance Enforcer 35 Focal Force PTA Balloon Catheter 6mm x 4cm, 5FR/80cm, Catalog Number ASB5-35-80-6-4, REF Number G35252 Product Usage: The Advance Enforcer 35 Focal-Force PTA Balloon Catheter is intended for percutaneous transluminal angioplasty (PTA) of lesions in…
Category
Medical Device
Distribution
Distributed nationwide

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