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

17001–17025 of 114192

HighFDA (Food)·F-1098-2024·2024-04-03
Barsotti Organic Carrot Juice recalled due to under-processing
Barsotti Organic Carrot Juice in 16 oz and 64 oz bottles (also sold under Trader Joe's label) is recalled because it was determined to be under-processed. This may allow harmful bacteria to survive.
Product
Barsotti Organic Carrot Juice 16 oz. and 64 oz. plastic bottles Perishable, Keep Refrigerated Ingredient: Fresh Pressed Organic Carrot Juice. Flash Pasteurized. Barsotti Juice Co., Camino, CA 95709 (530_ 622-4629 www.barsottijuice.com Trader Joe's 100% Juice Organic Carrot…
Category
Food
Distribution
10 states
HighFDA (Devices)·Z-1391-2024·2024-04-03
Puritan HydroFlock Collection Device Distributed with Wrong Product Code
Puritan Medical Products distributed HydroFlock Sterile Flocked Collection Devices labeled as Part Number 25-3317-H, Lot S1014 that actually contain product code 25-3317-U. Approximately 232,500 units were affected.
Product
HydroFlock Sterile Flocked Collection Device, Part Number 25-3317-H.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1366-2024·2024-04-03
MediBeads Neck Wrap recalled for potential mold and mildew growth
Bruder Healthcare Company is recalling 430 units of MediBeads Neck Wrap (Item 34320) because the product may have been exposed to excessive moisture, creating potential for mold and mildew growth. Lot Number M053300, distributed in the US and Canada.
Product
MediBeads Neck Wrap, Item Number 34320
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1094-2024·2024-04-03
Himalayan Pain Relief Tea Contains Undeclared Pharmaceutical Drugs
WS Global Inc is recalling Himalayan Pain Relief Tea nationwide due to undeclared pharmaceutical drugs—Diclofenac and Dexamethasone Acetate—that were not listed on the product label.
Product
Himalayan Pain Relief Tea for Gout and Hangover
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-1108-2024·2024-04-03
Emerald River Premium Thai Jasmine Rice Recalled for Glass Contamination
Otis McAllister recalls Emerald River Premium Thai Jasmine Rice due to glass contamination. The product was distributed in Utah, Oregon, Texas, and Washington.
Product
Product LAbeled in part: "Emerald River Premium Thai Jasmine Rice ... Net Wt 50 lb (22.7 kg) ... UPC 0 28571 00474 6"
Category
Food
Distribution
4 states
HighFDA (Devices)·Z-1361-2024·2024-04-03
Thermalon Sinus Compress Recalled for Potential Mold and Mildew
Bruder Healthcare Company is recalling 1,416 units of Thermalon Sinus Compress (Item Number 24332) due to potential mold and mildew growth from excessive moisture exposure. Affected lot numbers are M053160 and M053570.
Product
Thermalon Sinus Compress, Item Number 24332
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1390-2024·2024-04-03
Boston Scientific iSLEEVE Expandable Introducer Sets Recalled for Hemostatic Valve Leak
Boston Scientific is recalling specific batches of the iSLEEVE Expandable Introducer Set due to hemostatic valve leaks affecting 4,060 devices. The devices are distributed in the US, Canada, and worldwide.
Product
Boston Scientific iSLEEVE EXPANDABLE Introducer Set REF H74939349140, facilitates femoral access to the vascular system
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0419-2024·2024-04-03
Pharmaceutical Injection Recalled Due to Lack of Sterility Assurance
SCA Pharmaceuticals is recalling PHENYLephrine HCl 40 mg injection nationwide due to lack of sterility assurance. Patients should contact their healthcare provider and not use this product.
Product
PHENYLephrine HCl 40 mg in 0.9% Sodium Chloride Injection, (Concentration = 160 mcg/mL), 250 mL Bag, Rx Only, SCA Pharmaceuticals, 755 Rainbow Rd. Windsor, CT 06095, NDC 70004-0825-40, Bar Code 70004082540.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1369-2024·2024-04-03
Cystatin C Calibrator Series CVS 2699 Recalled for Calibration Bias
Randox Laboratories is recalling Cystatin C Calibrator Series CVS 2699 because it runs with negative bias compared to other methods, which could affect test accuracy on automated analyzers.
Product
Cystatin C Calibrator - In vitro diagnostic (IVD) use in the calibration of the Randox Cystatin C assay on automated analysers Catalog Number: CVS 2699
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1378-2024·2024-04-03
Baxter Supple Peri-Guard Repair Patch Recall Due to Endotoxin Contraindication
Baxter is recalling Supple Peri-Guard Repair Patch units due to elevated endotoxin levels that may exceed allowable limits for cerebrospinal fluid-contacting devices. The product should not be used in neurosurgery.
Product
Baxter Supple Peri-Guard Repair Patch (legacy product codes): a) PC0404SNBIO, b) PC0608NSBIO, c) PC0814SNBIO, d) PC1016SNBIO
Category
Medical Device
Distribution
5 states
HighNHTSA·24V247000·2024-04-03
Winnebago Recalls 2024 Access Trailers Due to GFCI Wiring Defect
Winnebago is recalling 2024 Access travel trailers because incorrectly wired GFCI outlets may lack protection, increasing the risk of electrical shock.
Product
WINNEBAGO — WINNEBAGO ACCESS
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1377-2024·2024-04-03
Baxter Peri-Guard Repair Patch contraindicated for neurosurgical use
Peri-Guard Repair Patch is now contraindicated for neurosurgery because its endotoxin level may exceed the limit allowable for cerebrospinal fluid-contacting devices. Product instructions have been updated.
Product
Baxter Peri-Guard Repair Patch (legacy product codes): a) PC0404NBIO, b) PC0608NBIO, c) PC0814NBIO, d) PC1016NBIO
Category
Medical Device
Distribution
5 states
HighNHTSA·24E031000·2024-04-03
Watson & Chalin Recalls SL2065 Steerable Lift Axle Suspension Systems
Watson & Chalin is recalling SL2065 steerable lift axle suspension systems because bearing journals may not be fully seated, creating a risk of spindle fracture and crash.
Product
STEERING:LINKAGES:KNUCKLE:SPINDLE:ARM recall
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1360-2024·2024-04-03
Thermalon Sinus Compress Recalled for Potential Mold and Mildew Growth
Bruder Healthcare Company is recalling certain lots of Thermalon Sinus Compress due to potential mold and mildew growth from moisture exposure. The product was distributed in the US and Canada.
Product
Thermalon Sinus Compress (French), Item Number 24332F
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0420-2024·2024-04-03
PHENYLephrine HCl Injectable Recalled Due to Lack of Sterility Assurance
SCA Pharmaceuticals is recalling PHENYLephrine HCl 800 mcg/10 mL injections due to lack of assurance of sterility. The recall affects 3,671 syringes distributed nationwide.
Product
PHENYLephrine HCl 800 mcg/10 mL in 0.9% Sodium Chloride Injection, (Concentration = 80mcg/mL) 10 mL fill 12 mL Syringe, Rx Only, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT 06095, NDC 70004-0816-12, Bar Code 700040081612.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1372-2024·2024-04-03
Laboratory performance verifier recalled for mismatched diluent assembly
Ortho-Clinical Diagnostics is recalling 10,911 units of VITROS Performance Verifier I worldwide due to mismatched diluent components that could cause inaccurate quality control test results.
Product
VITROS Performance Verifier I
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1103-2024·2024-04-03
German Home Bakery Apple Coffee Cake Recalled for Undeclared Wheat and Yellow #5
German Home Bakery Apple Coffee Cake is being recalled due to undeclared wheat and Yellow #5 food coloring. Consumers with wheat allergies or Yellow #5 sensitivity should not consume this product.
Product
German Home Bakery Apple Coffee Cake, 16 oz, clear poly bag
Category
Food
Distribution
1 state
HighFDA (Drugs)·D-0407-2024·2024-04-03
Hydromorphone Injection Recalled Due to Lack of Sterility Assurance
SCA Pharmaceuticals recalls 1,023 syringes of Hydromorphone Injection nationwide due to lack of sterility assurance. No illnesses have been reported.
Product
HYDROmorphone HCl 10 mg/50 mL in 0.9% Sodium Chloride Injection (Concentration = 0.2 mg/ml) 50 mL fill Syringe, Rx only, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT 06095, NDC 70004-0300-22, Bar Code 70004030022
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1368-2024·2024-04-03
Endoscopic Lens Cleaner Recalled for Instruction Discrepancy Risk
Olympus recalls InstaClear Lens Cleaner devices due to inconsistencies between Japanese and English instruction manuals that could cause component separation during endoscopic procedures.
Product
InstaClear Lens Cleaner-indicated for use during routine diagnostic procedures and during endoscopic sinus surgery. Model Number: LCS1500UNOL LCS1800UNST LCS4K00UNOL LCS1530BTOL LCS1830BTST LCS4K30BTOL LCS1530TPOL LCS1830TPST LCS4K30TPOL LCS1545BTOL LCS1845BTST…
Category
Medical Device
Distribution
0 states
HighFDA (Drugs)·D-0424-2024·2024-04-03
Succinylcholine Chloride Injection Recalled for Sterility Assurance Failure
SCA Pharmaceuticals is recalling 5,079 syringes of Succinylcholine Chloride Injection nationwide due to lack of sterility assurance. Affected lots are #1223049085 and #1223049364.
Product
SUCcinylcholine Chloride 100 mg/5mL Injection (Concentration = 20mg/mL), 5 mL fill 6 mL Syringe, Rx only, Repackaged by SCA Pharma, 755 Rainbow Rd., Windsor, CT 06095, NDC 70004-0908-09, Bar Code 70004090809
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1364-2024·2024-04-03
Thermalon Heating Pads Recalled for Potential Mold and Mildew Growth
Bruder Healthcare recalls Thermalon Heating Pad model 24002 due to potential mold and mildew growth from moisture exposure. Affected units were distributed nationwide in the US and to Canada.
Product
Thermalon Heating Pad, Item Number 24002
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1105-2024·2024-04-03
Coffee cake recalled for undeclared Yellow #5 food dye
Sunflour Bakery is recalling German Home Bakery Raspberry Coffee Cake due to undeclared Yellow #5 dye. The voluntary Class II recall affects 70 loaves distributed in California.
Product
German Home Bakery Raspberry Coffee Cake, 16 oz, clear poly bag
Category
Food
Distribution
1 state
ModerateFDA (Devices)·Z-1386-2024·2024-04-03
Philips Patient Information Center Custom Ringtones Fail When Screen Locked
Philips Patient Information Center iX running software version 4.X may not play custom ringtones when iOS screens are locked with a passcode. Approximately 257,183 units have been distributed worldwide. No injuries have been reported.
Product
Patient Information Center iX (PIC iX), Model Numbers 866389, 866390 (PIC iX Expand), and 866424 (PIC iX Hardware) running Software Version Number 4.X
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1363-2024·2024-04-03
Thermalon Neck Wrap recalled due to potential mold and mildew growth
Bruder Healthcare Company is recalling Thermalon Neck Wrap (Item Number 24322) from certain lots due to potential mold and mildew growth from excessive moisture exposure. Consumers should discontinue use and contact the manufacturer.
Product
Thermalon Neck Wrap, Item Number 24322
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1387-2024·2024-04-03
CareEvent Event Management System notification failure on locked iOS devices
The CareEvent Event Management System's Care Assist mobile application fails to play custom ringtones when iOS device screens are locked with a passcode. This may result in missed alerts or notifications.
Product
CareEvent Event Management System, Model Numbers 866435 and 866436 (CareEvent Upgrade), Software Version Number C.03.X
Category
Medical Device
Distribution
Distributed nationwide

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17001–17025 of 114192