The Recall Desk

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.

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6776–6800 of 7514

  • SevereFDA (Drugs)·D-0306-2022·2022-01-05

    Sodium Bicarbonate in 5% Dextrose Injection Recalled for Sterility Assurance

    SterRx is recalling Sodium Bicarbonate in 5% Dextrose Injection nationwide due to lack of assurance of sterility. The recall affects 127,260 bags distributed across the U.S.

    Product
    Sodium Bicarbonate in 5% Dextrose Injection, 150 mEq per 1000 mL (12.6 mg per mL), Rx only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-326-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0321-2022·2022-01-05

    SterRx Norepinephrine 8 mg Sodium Chloride Injection Recalled

    SterRx, LLC is recalling 74,508 bags of Norepinephrine 8 mg per 250 mL in 0.9% Sodium Chloride Injection nationwide due to lack of assurance of sterility. The FDA classified this as a Class II recall.

    Product
    NOREPINEPHRINE, 8 mg per 250 mL, (32 mcg per mL) in 0.9% Sodium Chloride Injection, Rx only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-676-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0304-2022·2022-01-05

    EPINEPHrine Injection Recall Due to Lack of Sterility Assurance

    SterRx is recalling EPINEPHrine 2 mg per 250 mL injectable solution nationwide due to lack of assurance of sterility. The recall affects 2,779 bags distributed across the U.S.

    Product
    EPINEPHrine, 2 mg per 250 mL (8 mcg per mL) in 0.9% Sodium Chloride Injection, Rx only, SterRx, 141 Idaho Ave., Plattsburgh, NY, 12903, NDC 70324-027-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0295-2022·2022-01-05

    Lidocaine Hydrochloride Topical Solution recalled for being superpotent

    Teligent Pharma has recalled 6,816 bottles of Lidocaine Hydrochloride Topical Solution 4% nationwide due to the drug being superpotent. The recall is voluntary and involves Lot #16345 with expiration date 01/2024.

    Product
    LIDOCAINE HYDROCHLORIDE — LIDOCAINE HYDROCHLORIDE (LIDOCAINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0350-2022·2021-12-29

    Dakota Tom's Chicken Salad Croissant Sandwiches Recalled for Undeclared Allergens

    Dakota Tom's and Market Fresh branded Chicken Salad Croissant sandwiches are being recalled because they contain undeclared egg and milk. Consumers who have allergies to these ingredients should not consume the product.

    Product
    Dakota Tom's and Market Fresh branded Chicken Salad Croissant sandwiches. Net Wt. 6.5 oz. UPC 37296-10100, Dakota Toms, Box 271, Corsica, SD 57328.
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Drugs)·D-0288-2022·2021-12-29

    Moxifloxacin 1 mg/mL Solution Label Mix-up Recall

    Denver Solutions, LLC (doing business as Leiters Health) is recalling Moxifloxacin 1 mg/mL intracameral injection solution because vials labeled as 1 mg/mL may actually contain 5 mg/mL, creating a serious dosing error risk.

    Product
    Moxifloxacin, 1 mg/mL, 1mL in 2mL vial, solution for intracameral injection, 10 vials/carton, Rx only, Leiters 13796 Compark Blvd, Englewood, CO 80112, (800) 292-6772, NDC 71449-096-42
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0292-2022·2021-12-29

    OTC Expectorant Recall: Microbial Contamination in Rompe Pecho

    Efficient Laboratories is recalling Rompe Pecho guaifenesin expectorant in 4 fl oz and 6 fl oz bottles due to microbial contamination of non-sterile products. The affected product was distributed nationwide.

    Product
    ROMPE PECHO — ROMPE PECHO (GUAIFENESIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0293-2022·2021-12-29

    OTC Cough and Cold Drug Recalled for Microbial Contamination

    Efficient Laboratories is recalling approximately 4,026 bottles of Rompe Pecho Max Multi-Symptoms cough and cold medicine nationwide due to potential microbial contamination of the non-sterile product.

    Product
    ROMPE PECHO MAX MULTI SYMPTOMS — ROMPE PECHO MAX MULTI SYMPTOMS (ACETAMINOPHEN, DEXTROMETHOPHAN HBR, PHENYLEPHRINE HCL, GUAIFENESIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0394-2022·2021-12-29

    WIRION Embolic Protection System Filter Withdrawal Difficulties

    Cardiovascular Systems Inc recalls WIRION Embolic Protection System devices (6Fr) because the filter assembly may become difficult to withdraw, and the device may tear or separate, creating a risk of blood clot embolization.

    Product
    WIRION EMBOLIC PROTECTION SYSTEM, Delivery Catheter and Filter and Retrieval Catheter, 6Fr, REF (Model Number) WRN-D6
    Category
    Medical Device
    Distribution
    38 states
  • SevereFDA (Devices)·Z-0383-2022·2021-12-29

    Stealthstation and Synergy Cranial surgical navigation system software synchronization error

    Stealthstation and Synergy Cranial surgical navigation systems may display an incorrect biopsy needle position due to software synchronization failure. This could result in prolonged surgery, additional procedures, or tissue injury.

    Product
    Stealthstation System w/ Stealthstation Cranial Software 3.1.1,3.1.2,3.1. or SynergyCranial Software. Synergy Cranial, Model: 9733763, and StealthStation Cranial, Model: 9735585
    Category
    Medical Device
    Distribution
    51 states
  • SevereCPSC·22714·2021-12-23

    Polaris RZR and GENERAL Recreational Off-Road Vehicles Steering Wheel Separation Recall

    Polaris is recalling about 8,800 RZR and GENERAL recreational off-road vehicles because the steering wheel can separate, causing loss of control and crash risk. Polaris has received 33 reports of broken or cracked steering wheel spokes, including five rollovers and two injuries.

    Product
    Polaris RZR and GENERAL Recreational Off-Road Vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·22036·2021-12-22

    Angel Line Bunk Beds with Angled Ladders Recalled for Entrapment and Strangulation Risk

    Longwood Forest is recalling Angel Line bunk beds with angled ladders because the metal hook fastening the ladder can detach or move, creating gaps that pose serious entrapment and strangulation hazards. A 2-year-old child died in May 2018 when found unresponsive in a bunk bed ladder gap.

    Product
    Angel Line Bunk Beds with angled ladders
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalCPSC·22040·2021-12-22

    Carex Adult Portable Bed Rails Recalled After Three Deaths

    Compass Health Brands is recalling Carex Brand Adult Portable Bed Rails due to entrapment and asphyxiation hazards. Three deaths have been reported when users became trapped within the rails or between the rail and mattress.

    Product
    Carex Brand Adult Portable Bed Rails
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalCPSC·22037·2021-12-22

    Royal Sovereign Portable Air Conditioners Recalled for Fire and Burn Hazards

    Royal Sovereign International is recalling about 33,570 portable air conditioners due to a faulty drain motor that can ignite the plastic enclosure, causing fires and burns. One death from smoke inhalation has been reported, along with 11 incidents of fires or smoking and over $1 million in property damage.

    Product
    Royal Sovereign/Royal Centurian portable air conditioners
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalCPSC·22039·2021-12-22

    Essential Medical Supply Endurance Hand Bed Rails Due to Entrapment and Asphyxiation

    Essential Medical Supply is recalling approximately 272,000 Endurance Hand Bed Rails because users can become entrapped within the rail or between the rail and mattress, posing a risk of asphyxiation. One death has been reported.

    Product
    Endurance® Hand Bed Rails
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0280-2022·2021-12-22

    Lidocaine Topical Solution Recalled for Superpotency

    Teligent Pharma, Inc. is recalling Lidocaine Hydrochloride Topical Solution USP 4% nationwide due to the drug being superpotent. Affected lots are 13262 (Exp. 03/2022) and 14217 (Exp. 08/2022).

    Product
    Lidocaine Hydrochloride Topical Solution USP 4% (40 mg/mL), 50 mL glass bottles, Rx Only, Teligent Pharma Inc., Buena, NJ 08310, NDC 52565-009-50
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0358-2022·2021-12-22

    Livia One Organic Daily Topical Spray Probiotics recalled for Pseudomonas contamination

    Livia Global is recalling Livia One Organic Daily Topical Spray Probiotics because the product may be contaminated with Pseudomonas aeruginosa, a bacterium that can cause infection.

    Product
    Livia One Organic Daily Topical Spray Probiotics; 4 oz. (120 ml) UPC: 0 30915 10710 5 Recommended use: Topical: Spray affected area 2-5 times daily as needed. Ingredients: Proprietary probiotic blend in an enzyme enriched substrate: Lactobacillus-Acidophilus, L. Rhamn
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Food)·F-0286-2022·2021-12-22

    Al Kanater Tahini Sesame Seeds Recalled for Salmonella

    International Golden Foods Inc is recalling Al Kanater Tahini Sesame Seeds (1 lb plastic bottles) due to potential Salmonella contamination. The affected product was distributed to retailers and distributors in Illinois and Michigan.

    Product
    Al Kanater Tahini Sesame Seeds. 1 Lb plastic bottle. UPC 6-92551-00002-0
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-0322-2022·2021-12-22

    Country Time Lemonade Drink Mix Powder Recalled for Glass and Metal Contamination

    Kraft Heinz Foods Company is recalling Country Time Lemonade drink mix powder in five sizes due to potential contamination with glass and metal fragments. The recall affects approximately 289,221 cases distributed nationwide and internationally.

    Product
    Country Time Lemonade drink mix powder 19 oz. UPC 043000951170 29 oz. UPC 043000951194 63 oz. UPC 043000082195 82.5 oz. UPC 043000928608 116 oz. UPC 043000075388
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereCPSC·22034·2021-12-22

    Hang-on Treestands Recalled Due to Cable Failure and Fall Hazard

    Big Game Treestands' 2021 The Captain model (batch 2M-0121) is recalled because plastic-coated cable crimps can slip during use, releasing the standing platform and causing falls. Two injuries have been reported from ten documented incidents.

    Product
    The Captain Hang-on Treestands (2021 Batch #2M-0121)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0337-2022·2021-12-22

    FDA Class I Recall: Cardiosave Rescue Intra-Aortic Balloon Pump Fluid Ingress

    Datascope is recalling Cardiosave Rescue Intra-Aortic Balloon Pump devices due to possibility of fluid ingress, which could short electronic components and cause unsafe system shutdown.

    Product
    Cardiosave Rescue IntraAortic Balloon Pump. Model Numbers: 0998-00-0800-75, 0998-UC-0800-75, 0998-00-0800-83, 0998-UC-0800-83, 0998-00-0800-85, 0998-UC-0800-85.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0336-2022·2021-12-22

    Cardiosave Hybrid IntraAortic Balloon Pump Recall Due to Fluid Ingress Risk

    Datascope Corp. is recalling Cardiosave Hybrid IntraAortic Balloon Pumps due to the risk of fluid entering the device, which could cause system failure and hemodynamic instability.

    Product
    Cardiosave Hybrid IntraAortic Balloon Pump. Model Numbers: 0998-00-0800-31, 0998-UC-0800-31, 0998-00-0800-32, 0998-UC-0800-32, 0998-00-0800-33, 0998-UC-0800-33, 0998-00-0800-34, 0998-UC-0800-34, 0998-00-0800-35, 0998-UC-0800-35, 0998-00-0800-36, 0998-UC-0800-36, 0998-00-0800-45,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V990000·2021-12-17

    2020 Mercedes-Benz A220 suspension recall due to corroding axle carrier

    Mercedes-Benz is recalling certain 2019-2020 A220 and other model vehicles because the front axle carrier may corrode and fail, potentially causing loss of steering control. Dealers will inspect and replace the carrier for free.

    Product
    MERCEDES-BENZ — 2020 MERCEDES-BENZ A220
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V979000·2021-12-16

    2021-2022 Ford Mustang Mach-E and 2022 Maverick seat belt attachment recall

    Ford is recalling 2021-2022 Mustang Mach-E and 2022 Maverick vehicles due to improperly attached rear seat belt buckles. The defect may prevent proper occupant restraint in a crash, creating an injury risk.

    Product
    FORD — 2021 FORD MUSTANG MACH E
    Category
    Vehicle
    Distribution
    Distributed nationwide