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.

Filters

Agency

Category

Minimum severity

Clear filters

9251–9275 of 36630

  • SevereFDA (Drugs)·D-0710-2021·2021-08-18

    Morphine-Bupivacaine Injectable Recalled for Non-Sterility

    Med Shop Total Care Inc. is recalling morphine-bupivacaine injectable in prefilled syringes of multiple strengths due to non-sterility. The affected product was distributed to Texas and Puerto Rico.

    Product
    MORPHINE-BUPIVACAINE PF INJECTABLE 21 mL, 22 mL, 23 mL, 41 mL and 43 mL syringes in various strengths: a) 20MG/ML-40MG/ML, b) 15MG-30MG/ML, c) 5MG/ML-20MG/ML, d) 2MG-30MG/ML, e) 20MG-5MG/ML, f) 15MG-5MG/ML, g) 5MG-2MG/ML, h) 5MG-11MG/ML, i) 20MG-6MG/ML, j) 10MG-10MG/ML, k) 6MG-4.
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0705-2021·2021-08-18

    Injectable drug recalled for non-sterility in Texas and Puerto Rico

    Med Shop Total Care Inc. is recalling a Bupivacaine HCL-Lioresal PF injectable drug due to non-sterility concerns. The recall affects a 41 mL syringe product distributed in Texas and Puerto Rico.

    Product
    BUPIVACAINE HCL-LIORESAL PF INJECTABLE 7.5MG-1625MCG/ML, 41 mL syringe, Rx only, Med Shop Total Care 470 East Loop 281 Longview, TX 75605
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Food)·F-0871-2021·2021-08-18

    Dark Chocolate Malt Balls recalled for undeclared peanuts

    DSD Merchandisers is recalling Dark Chocolate Malt Balls because some containers were filled with Dark Chocolate Peanut Butter malt balls instead, creating a risk for consumers with peanut allergies who may not be aware of the peanut content.

    Product
    Dark Chocolate Malt Balls in plastic container; 9 oz./ 255g UPC: 6 5143370179 0 Packed on the same equipment as products that contain milk, eggs, tree nuts, peanuts, wheat and soy. Distributed by DSD Merchandisers, Inc., Livermore, CA 64551
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-0899-2021·2021-08-18

    McCormick Culinary Italian Seasoning Recalled for Salmonella Risk

    McCormick & Company is recalling McCormick Culinary Italian Seasoning (1.75 lbs. plastic jugs) distributed across multiple U.S. states and Canada due to potential Salmonella contamination.

    Product
    McCormick Culinary Italian Seasoning 1.75 lbs. , Plastic Jugs (Large Plastic Bottles), (3) 3 packages per case.
    Category
    Food
    Distribution
    15 states
  • SevereFDA (Drugs)·D-0716-2021·2021-08-18

    Injectable Drug Recalled for Non-Sterility Risk

    Med Shop Total Care Inc. is recalling a compounded injectable drug containing hydromorphone, bupivacaine, and sufentanil due to non-sterility concerns. The drug was distributed in Texas and Puerto Rico.

    Product
    HYDROMORPHONE HCL-BUPIVACAINE HCL-SUFENTANIL PF 25MG-9MG-110MCG/ML INJECTABLE 21 mL syringe, Rx only, Med Shop Total Care 470 East Loop 281 Longview, TX 75605
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0714-2021·2021-08-18

    Injectable Drug Sufentanil-Bupivacaine-Baclofen Recalled for Non-Sterility

    Med Shop Total Care Inc. is recalling a 41 mL injectable drug combination due to non-sterility concerns. The affected product was distributed in Texas and Puerto Rico.

    Product
    SUFENTANIL-BUPIVACAINE-BACLOFEN PF 25MCG-12.5MG-750MCG/ML INJECTABLE 41 mL syringe, Rx only, Med Shop Total Care 470 East Loop 281 Longview, TX 75605
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0718-2021·2021-08-18

    Compounded Progesterone Oil Recalled for Non-Sterility Risk

    People's Custom Rx is recalling C-Progesterone Oil 100 mg/mL compounded vials due to non-sterility concerns. The recall affects 14 vials distributed in Mississippi and Tennessee.

    Product
    C-PROGESTERONE OIL 100 MG/ML, 10 mL vials, Compound, People's Custom Rx, Compounded, Rx only, People's Custom Rx, 785 E Brookhaven Cir, Memphis, TN 38117
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Devices)·Z-2165-2021·2021-08-18

    Spectrum IQ Infusion Pump Safety Software Recalled for Drug Identifier Mismatch

    Baxter is recalling Dose IQ Safety Software for Spectrum IQ Infusion Pumps due to a software defect that creates a mismatch between displayed drug names and the device's drug library. This could lead to incorrect medication administration.

    Product
    Dose IQ Safety Software used with Spectrum IQ Infusion Pump
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2204-2021·2021-08-18

    Infusion Pump Module Bezel Repair Parts Recalled for Infusion Hazards

    BioMedical Equipment Service Co (BMES) recalls bezel repair parts for Alaris Infusion Pump Module Model 8100. Non-original parts may crack or separate, causing free flow, over-infusion, under-infusion, or interruption of infusion.

    Product
    Alaris Infusion Pump Module, Model 8100, serviced/repaired by Biomedical Equipment Service Co. (BMES) with an impacted bezel repair part TIPA-8100-4410
    Category
    Medical Device
    Distribution
    9 states
  • SevereFDA (Drugs)·D-0717-2021·2021-08-18

    Hydromorphone HCL-Bupivacaine HCL Injectable Recalled for Non-Sterility

    Med Shop Total Care Inc. is recalling Hydromorphone HCL-Bupivacaine HCL PF Injectable in 21 and 22 mL syringes in various strengths distributed in Texas and Puerto Rico due to non-sterility concerns.

    Product
    HYDROMORPHONE HCL-BUPIVACAINE HCL PF INJECTABLE 21 and 22 mL syringes in various strengths: a) 0.5MG-5MG/ML, b) 2MG-35MG/ML, c) 25MG-15MG/ML, d) 6MG-1.5MG/ML, e) 3MG-3MG/ML, f) 5MG-15MG/ML, g)12MG-8MG/ML, h)2MG-2MG/ML, i) 30MG-30MG/ML, j) 8MG-20MG/ML, k) 20MG-10MG/ML, l)50MG-3.5M
    Category
    Drug
    Distribution
    2 states
  • SevereCPSC·21186·2021-08-18

    Ravin White Arrow Nocks Recalled for Injury Risk

    Ravin Crossbows is recalling white arrow nocks that can fail to engage properly with the bowstring, allowing the crossbow to discharge unexpectedly during re-nocking and causing finger injuries. About 220,000 units are affected.

    Product
    Ravin® white arrow nocks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0713-2021·2021-08-18

    Morphine-Bupivacaine-Ketamine Injectables Recalled for Non-Sterility

    Med Shop Total Care Inc. is recalling Morphine-Bupivacaine-Ketamine PF Injectable syringes distributed in Texas and Puerto Rico due to non-sterility. The injectable comes in two strengths in 21 mL syringes and is available by prescription only.

    Product
    MORPHINE-BUPIVACAINE-KETAMINE PF INJECTABLE 21 mL syringe in two strengths: a) 5MG-25MG-5MG/ML, b) 1MG-2MG-100MCG/ML, Rx only, Med Shop Total Care 470 East Loop 281 Longview, TX 75605
    Category
    Drug
    Distribution
    2 states
  • SevereNHTSA·21E076000·2021-08-18

    Palfinger Knuckle Boom Cranes Recalled Due to Base Cracking Risk

    Palfinger is recalling specific Knuckle Boom Cranes because the base may crack, potentially causing the crane to detach from the truck mount.

    Product
    EQUIPMENT:MECHANICAL:BOOM/CRANE/LADDER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·21179·2021-08-17

    Zen Magnets and Neoballs Magnets Recalled Due to Ingestion Hazard

    Zen Magnets and Neoballs high-powered spherical magnets are being recalled because swallowing multiple magnets can cause intestinal perforation, blockage, and death. About 10 million magnets sold individually and in sets since January 2009 are affected.

    Product
    Zen Magnets and Neoballs Magnets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V634000·2021-08-12

    Utility Bodywerks Recalls Ram 4500 and 5500 Trucks for Brake Line Defect

    Utility Bodywerks is recalling 2019-2020 Ram 4500 and 5500 trucks because improperly routed rear brake lines may chafe and leak, increasing crash risk.

    Product
    UTILITY BODYWERKS — UTILITY BODYWERKS RAM 4500, RAM 5500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V633000·2021-08-12

    GM Recalls 2013 Buick and Chevrolet Vehicles for Rear Suspension Defect

    General Motors is recalling 2013 Buick Regal, Lacrosse, and Chevrolet Malibu vehicles because excessive corrosion protection on rear toe links may cause them to fracture, increasing crash risk.

    Product
    CHEVROLET — CHEVROLET, BUICK MALIBU, LACROSSE, REGAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21E074000·2021-08-12

    Chrysler Recalls Mopar Side Air Bag Inflatable Curtains Due to Inflator Defect

    Chrysler is recalling Mopar side air bag inflatable curtains sold as replacement parts because the inflator end cap may detach or the sidewall may rupture, posing an injury risk.

    Product
    AIR BAGS:SIDE/WINDOW:CURTAIN:INFLATOR recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V635000·2021-08-12

    Land Rover Recalls LR4 and Range Rover Sport for Fuel Leak Risk

    Jaguar Land Rover is recalling 2010-2016 LR4 and 2010-2013 Range Rover Sport vehicles because a fuel tank flange may crack, causing a leak that increases fire risk.

    Product
    LAND ROVER — LAND ROVER LR4, RANGE ROVER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0825-2021·2021-08-11

    Great Value Chocolate Chip Snack Muffins Recalled for Listeria Contamination

    Give and Go Prepared Foods is recalling Great Value Chocolate Chip Snack Muffins nationwide because they may be contaminated with Listeria monocytogenes, a harmful bacterium that can cause serious foodborne illness.

    Product
    Great Value Chocolate Chip Snack Muffin - 12 oz, 8 per case; UPC 078742-33100 3
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0702-2021·2021-08-11

    Succinylcholine Chloride Syringes Recalled for Lack of Sterility Assurance

    BayCare Central Pharmacy is recalling Succinylcholine Chloride 100 mg/5 mL syringes due to lack of sterility assurance. The affected lot was distributed in Florida.

    Product
    Succinylcholine Chloride 100 mg/5 mL (20 mg/mL), 5 mL Syringes, Rx only, For IV Use only, BayCare Central Pharmacy, 7802 E. Telecom Parkway, Temple Terrace, FL 33837
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Food)·F-0811-2021·2021-08-11

    Grimmway Farms Shredded Carrots Recall for Salmonella Contamination

    Grimmway Farms is recalling shredded carrots due to potential Salmonella contamination. The product was distributed nationwide in multiple package sizes including retail bags and food service containers.

    Product
    Shredded Carrots Brand name: Grimmway Farms 10 oz. (284g) plastic bag UPC: 0 7878350610 1 10 oz. plastic bags - Kroger - did not reach retail. Destroyed at DC's 10 oz. plastic bags - LIDL - Did not reach retail. Destroyed at DC's 5 lb. bags - Food Service - Brand Nam
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0809-2021·2021-08-11

    Organic Petite Carrots Recalled for Potential Salmonella Contamination

    Grimmway Enterprises is recalling organic petite carrots sold under multiple brands due to potential Salmonella contamination. The FDA has classified this as a Class I recall affecting approximately 62,582 cases distributed nationwide.

    Product
    Organic Petite Carrots Brand name: Cal-Organic, 12 oz. (340g) plastic bag UPC: 0 7878390810 3 Organic Premium Petite Carrots; Brand name: Bunny Luv 3 lb. (1.36kg) bag; UPC: 0 7878351301 7 12 oz. plastic Bag -whole Foods 365 brand 12 oz. plastic bag - Whole Foods 3
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0810-2021·2021-08-11

    Organic Baby Carrots Recalled Due to Salmonella Contamination Risk

    Grimmway Farms is recalling Bunny Luv brand organic cut and peeled baby carrots nationwide due to potential Salmonella contamination. Affected products are 1 lb. bags with lot codes beginning with 195, 196, or 197 and ending in BF or SP.

    Product
    Organic Cut and Peeled Baby Carrots Brand name: Bunny Luv 1 lb.(454 g) plastic bag UPC: 0 3338390205 0;
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0816-2021·2021-08-11

    Grimmway Farms Carrot Chunks Recalled for Potential Salmonella

    Grimmway Enterprises, Inc. is recalling peeled carrot chunks sold in bulk because they may be contaminated with Salmonella. Consumers should not consume the affected product and should contact their retailer or the company for more information.

    Product
    Carrots Chunk Peeled 2" Grimmway Farms Sold in bulk - 50 lb., 25 lbs.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0813-2021·2021-08-11

    Organic Baby Rainbow Carrots Recalled for Potential Salmonella Contamination

    Grimmway Enterprises is recalling O Organics brand Organic Baby Rainbow Carrots due to potential Salmonella contamination. The FDA has classified this as a Class I recall affecting products nationwide.

    Product
    Organic Baby Rainbow Carrots Brand name: O Organics 12 oz. (340 g) plastic bag UPC: 0 7989398162 8 12 oz. bag - Wegmans. Did not reach retail. Destroyed at DC's 12 oz. bag - GreenWise. Dis not reach retail, Destroyed at DC's
    Category
    Food
    Distribution
    Distributed nationwide