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

27426–27450 of 114590

HighFDA (Devices)·Z-0146-2023·2022-11-09
Fogarty Arterial Embolectomy Catheters Recalled for Latex Deterioration
Edwards Lifesciences is recalling 715,620 Fogarty Arterial Embolectomy Catheters due to confirmed latex deterioration in the pouch packaging. The material degradation could affect device performance during use.
Product
Fogarty Arterial Embolectomy Catheters Model Number: 120602FP 120403FP 120803FP 120404FP 120804FP 120805FP 120806FP 120807FP Fogarty Arterial Embolectomy Catheter with Stylet Model Number: 120403FSP 120803FSP
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0031-2023·2022-11-09
FDA Recalls Cefuroxime Intravitreal Injections for Sterility Defect
Pharmacy Plus Inc. recalls 460 syringes of compounded Cefuroxime intravitreal solution distributed in Alabama, Louisiana, Mississippi, and Tennessee due to manufacturing sterility defect.
Product
CEFUROXIME INTRAVITREAL SYR 1MG/0.1ML Solution in 1 mL syringe, Rx only, Vital Care Compounder, 115 S. 40th Ave., Hattiesburg, MS 39402
Category
Drug
Distribution
4 states
HighFDA (Drugs)·D-0055-2023·2022-11-09
Sterile Talc Powder Recalled Due to Sterility Assurance Failure
Pharmacy Plus, Inc. is recalling sterile talc powder vials after FDA inspection found the manufacturing process cannot guarantee sterility. The product was distributed in Alabama, Louisiana, Mississippi, and Tennessee.
Product
TALC, STERILE POWDER, 5 GM vial, Rx only, Vital Care Compounder, 115 S. 40th Ave., Hattiesburg, MS 39402
Category
Drug
Distribution
4 states
HighFDA (Drugs)·D-0049-2023·2022-11-09
Prescription Injectable Medication Recalled for Sterility Assurance Failure
Pharmacy Plus, Inc. recalled a prescription injectable medication (Papaverine/Phentolamine/Prostaglandin) because FDA inspection found the product was produced in a manner that cannot guarantee sterility. Lot 65976 (BUD 10/27/2022) was distributed in AL, LA, MS, and TN.
Product
PAPAVERINE/PHENTOLAMINE/PROSTAGLANDIN INJ 150MG/5MG/10MCG/VIAL SOLUTION, 5 ML vial, Rx only, Vital Care Compounder, 115 S. 40th Ave., Hattiesburg, MS 39402
Category
Drug
Distribution
4 states
HighFDA (Food)·F-0094-2023·2022-11-09
Pesto Recall: Undisclosed Milk Allergen Not Listed on Label
Bella Cucina Artful Food Arugula & Pine Nut Pesto jars do not properly disclose milk on the label despite containing the allergen. The FDA Class II recall affects multiple lot numbers distributed nationwide and internationally.
Product
Bella Cucina Artful Food Arugula & Pine Nut Pesto Net Wt. 6 oz (169g) jar, UPC 6 19193 00145 1 Manufactured by Bella Cucina Artful Food Atlanta, GA 30310
Category
Food
Distribution
45 states
HighFDA (Food)·F-0103-2023·2022-11-09
Preserved Lemon Cream Recalled for Undisclosed Milk Allergen
Bella Cucina Artful Food is recalling its Preserved Lemon Cream because the label does not indicate the presence of milk, posing a risk to consumers with milk allergies.
Product
Bella Cucina Artful Food Preserved Lemon Cream Net Wt. 6 oz (169g) jar, UPC 6 19193 00045 4 Manufactured by Bella Cucina Artful Food Atlanta, GA 30310
Category
Food
Distribution
45 states
HighFDA (Devices)·Z-0169-2023·2022-11-09
Cardiac Navigation Catheter Recalled for Cellulose Fiber Contamination
Johnson & Johnson is recalling 91 THERMOCOOL SMARTTOUCH SF cardiac catheters nationwide due to manufacturing defects introducing cellulose fibers into the irrigation system. The contamination may prevent proper flushing, reduce cooling capability, or cause clotting complications.
Product
THERMOCOOL SMARTTOUCH SF Bi-Directional Navigation Catheter, REF: D-1348-05-S. Used for catheter-based cardiac electrophysiological mapping (stimulation and recording) and, in conjunction with an RF generator, for cardiac ablation.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0093-2023·2022-11-09
Bella Cucina Artichoke Lemon Pesto Recalled for Undeclared Milk Allergen
Bella Cucina Artful Food is recalling Artichoke Lemon Pesto in three sizes because the label does not declare milk as an ingredient. The product was distributed to all U.S. states, Canada, and Italy.
Product
Bella Cucina Artful Food Artichoke Lemon Pesto Net Wt. 3.5 oz (100g) UPC 6 19193 00232 8, Net Wt. 17 oz (xxxg) UPC 6 19193 00132 1 & Net Wt. 23 oz (652g) UPC 6 1913 00130 7 in glass jar, Manufactured by Bella Cucina Artful Food Atlanta, GA 30310
Category
Food
Distribution
45 states
HighFDA (Devices)·Z-0178-2023·2022-11-09
Beach Chair Clamp Shoulder Positioner recalled for adhesive curing failure
Baxter Healthcare recalls Beach Chair Clamp shoulder positioner components because adhesive on the fasteners may not cure properly, potentially reducing the device's mechanical integrity during surgical procedures.
Product
Beach Chair Clamp, BEACH CHAIR SHLDER POSITIONER CMPT, REF A-90013, #800104. Component to position and support the patients head in surgical procedures.
Category
Medical Device
Distribution
4 states
HighFDA (Devices)·Z-0177-2023·2022-11-09
Allen Spine Positioner Components Recalled for Adhesive Curing Defect
Baxter Healthcare is recalling Allen Standard Starburst spine positioning components due to adhesive that may not cure correctly, potentially compromising mechanical holding force in surgical head positioning devices.
Product
Allen Standard Starburst, Mayfield/Doro, STANDARD SPINE POSITIONERS CMPT, REF A-70710, #800103. Component to position and support the patients head in surgical procedures.
Category
Medical Device
Distribution
4 states
HighFDA (Food)·F-0101-2023·2022-11-09
Bella Cucina Sun-Dried Tomato Pesto Recalled for Undeclared Milk Allergen
Bella Cucina Artful Food sun-dried tomato pesto is being recalled because the label does not indicate the presence of milk, a major allergen. Consumers with milk allergies are at risk.
Product
Bella Cucina Artful Food Sun-Dried Tomato Pesto Net Wt. 3 oz (84.5g) jar, UPC 6 19193 00213 7 Manufactured by Bella Cucina Artful Food Atlanta, GA 30310
Category
Food
Distribution
45 states
HighFDA (Devices)·Z-0167-2023·2022-11-09
NICU PICC Insertion Bundle Recalled for Breather Pouch Seal Defects
Medline Industries recalls NICU PICC insertion bundles (50 kits) due to openings in breather pouch seals that compromise sterile barrier integrity. This Class II recall affects units distributed across the United States.
Product
CENTURION MEDICAL PRODUCTS NICU PICC INSERTION BUNDLE W/O, REF CVI4470. Convenience kit used in medical procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0024-2023·2022-11-09
Buprenorphine and Naloxone Sublingual Tablets Recalled for Foreign Substance
Sun Pharmaceutical is recalling buprenorphine and naloxone sublingual tablets (8 mg/2 mg) due to a foreign substance. Affected lots DNC1129A and DNC1740A were distributed nationwide.
Product
BUPRENORPHINE AND NALOXONE — BUPRENORPHINE AND NALOXONE (BUPRENORPHINE AND NALOXONE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0129-2023·2022-11-09
Hood Lowfat Cottage Cheese recalled due to plastic foreign objects
HP Hood LLC is recalling Hood Lowfat Cottage Cheese (16 oz and 24 oz) with best-by dates Oct 24–Dec 12, 2022, because the product may contain plastic foreign objects.
Product
Hood Lowfat Cottage Cheese, 16 oz and 24 oz
Category
Food
Distribution
39 states
HighFDA (Devices)·Z-0163-2023·2022-11-09
Medline LINQ Surgical Trays Recalled for Compromised Pouch Seals
Medline has recalled LINQ TRAY surgical kits with breather pouch seal openings that could compromise sterility. The recall affects 40 kits distributed nationwide; no injuries have been reported.
Product
MEDLINE LINQ TRAY, REF DYNJ65880A. Convenience kit used in medical/surgical procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0160-2023·2022-11-09
Surgical Cataract Kits Recalled for Defective Breather Pouch Seals
Medline has recalled Bausch + Lomb cataract surgical kits due to breather pouches with seal openings that could compromise sterility. Affected kits were distributed nationwide.
Product
BAUSCH + LOMB CATARACT TRAY, REF LYN023FACTB. Convenience kit used in surgical procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0159-2023·2022-11-09
Surgical eye kits recalled for breached sterile pouches
Medline Industries recalls Bausch + Lomb eye muscle surgical kits due to breached breather pouches that may compromise sterility. The affected kits (Lot 22DBN366) were distributed nationwide.
Product
BAUSCH + LOMB EYE MUSCLE, REF VAL036EMESB. Convenience kit used in surgical procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0028-2023·2022-11-09
FDA Recalls Vital Care Autologous Tears Serum Due to Sterility Assurance Failure
Vital Care Compounder's Autologous Tears Serum Full Strength has been recalled due to manufacturing defects that cannot assure product sterility. The product was distributed in Alabama, Louisiana, Mississippi, and Tennessee.
Product
AUTOLOGUS TEARS SERUM SOLN FULL STRENGTH, 3 mL droptainers, Rx only, Vital Care Compounder, 115 S. 40th Ave., Hattiesburg, MS 39402
Category
Drug
Distribution
4 states
HighFDA (Devices)·Z-0161-2023·2022-11-09
Surgical Cataract Packs with Compromised Breather Pouch Seals Recalled
Medline recalls 708 Bausch + Lomb cataract surgical packs due to breather pouch seal defects that could compromise sterility of surgical instruments.
Product
BAUSCH + LOMB CATARACT PACK, REF VAL001CPMEA. Convenience kit used in surgical procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0095-2023·2022-11-09
Bella Cucina Pastry Tarts Recalled for Undisclosed Milk Allergen
Bella Cucina Artful Food is recalling Crostata Sweet Butter Pastry Tarts because the label fails to indicate the presence of milk, a major allergen. Affected units were distributed across all U.S. states and internationally.
Product
Bella Cucina Artful Food CROSTATA SWEET BUTTER PASTRY TARTS Net Wt. 2.6 oz (73g) box, Distributed by Bella Cucina Artful Food Atlanta, GA 30310 UPC 6 19193 00721 7
Category
Food
Distribution
45 states
HighFDA (Drugs)·D-0033-2023·2022-11-09
Glycerin Ophthalmic Drops Recalled Due to Sterility Manufacturing Concerns
Pharmacy Plus, Inc. dba Vital Care Compounder is recalling Glycerin Ophthalmic Drops 98.5% Solution because manufacturing methods cannot guarantee the sterility of the product. Products affected are distributed in Alabama, Louisiana, Mississippi, and Tennessee.
Product
GLYCERIN OPHTHALMIC DROPS 98.5% Solution, 10 mL droptainer, Rx only, Vital Care Compounder, 115 S. 40th Ave., Hattiesburg, MS 39402
Category
Drug
Distribution
4 states
HighFDA (Food)·F-0104-2023·2022-11-09
Bella Cucina Sweet Pumpkin Pesto fails to declare milk allergen
Bella Cucina Sweet Pumpkin Pesto (6 oz jars, UPC 6 19193 00144 4) does not indicate milk on the label, posing a risk for consumers with milk allergies. The product was distributed across most US states, Canada, and Italy.
Product
Food Sweet Pumpkin Pesto Net Wt. 6 oz (169g) jar, UPC 6 19193 00144 4 Manufactured by Bella Cucina Artful Food Atlanta, GA 30310
Category
Food
Distribution
45 states
HighFDA (Food)·F-0097-2023·2022-11-09
Bella Cucina Dried Cherry and Almond Biscotti Recalled for Undeclared Milk and Wheat
Bella Cucina Artful Food is recalling Dried Cherry and Almond Biscotti because the label fails to indicate the presence of milk and wheat allergens. Consumers with allergies to these ingredients should not consume the product.
Product
Bella Cucina Artful Food Dried Cherry and Almond Biscotti Net Wt. 6 oz (170g) bag, UPC 6 19193 00019 5 Distributed by Bella Cucina Artful Food Atlanta, GA 30310
Category
Food
Distribution
45 states
HighFDA (Devices)·Z-0151-2023·2022-11-09
Boston Scientific EMBLEM S-ICD Subcutaneous Defibrillators Software Defect Causes Battery Display Error
Boston Scientific is recalling 7 EMBLEM S-ICD Model A209 subcutaneous defibrillators due to a software defect that displays inaccurate battery capacity information. Patients may not realize when their device's battery requires replacement.
Product
EMBLEM S-ICD, Subcutaneous Implantable Defibrillators, Model A209, sterile.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0132-2023·2022-11-09
Pasta Salad Products Recalled for Undeclared Cashew Allergen
Craftology and Dutch Treat Foods pasta salads are recalled due to undeclared cashew allergen. The products were distributed in Michigan.
Product
Craftology This Is My Happy Place Handcrafted Pasta Salad 14oz clear plastic clamshell, UPC 8 55034 00649 4, 6 units per wholesale case. Dutch Treat Foods Sweet Pea Pasta Salad 10 pound case (2, 5 pound plastic bags per case), 20 pound and 30 pound buckets
Category
Food
Distribution
1 state

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27426–27450 of 114590