Browse the most recent U.S. safety recalls in our connected official government data.
3,525 recalls in our current data. Showing 701–800, newest first.
An inaccurate state-of-charge reading can lead to an unexpected loss of drive power, increasing the risk of crash. Additionally, a high voltage battery fire increases the risk of i…
Company / brand: Ford Motor Company recalls
Official ID 26E063000 · Official record ↗
Failed Dissolution Specifications. Notification from the manufacturer that lot is being recalled due to failed dissolution
Company / brand: Golden State Medical Supply recalls
Official ID EVT-99732-3aiyt7 · Official record ↗
Contaminated with Salmonella
Company / brand: Lexunder recalls
Official ID EVT-99582-2r09zi · Official record ↗
The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is…
Company / brand: Cardinal Health 200 recalls
Official ID Z-3105-2026 · Official record ↗
The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is…
Company / brand: Cardinal Health 200 recalls
Official ID Z-3104-2026 · Official record ↗
The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is…
Company / brand: Cardinal Health 200 recalls
Official ID Z-3103-2026 · Official record ↗
The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is…
Company / brand: Cardinal Health 200 recalls
Official ID Z-3102-2026 · Official record ↗
The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is…
Company / brand: Cardinal Health 200 recalls
Official ID Z-3101-2026 · Official record ↗
The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is…
Company / brand: Cardinal Health 200 recalls
Official ID Z-3100-2026 · Official record ↗
The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is…
Company / brand: Cardinal Health 200 recalls
Official ID Z-3099-2026 · Official record ↗
The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is…
Company / brand: Cardinal Health 200 recalls
Official ID Z-3098-2026 · Official record ↗
The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is…
Company / brand: Cardinal Health 200 recalls
Official ID Z-3097-2026 · Official record ↗
The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is…
Company / brand: Cardinal Health 200 recalls
Official ID Z-3096-2026 · Official record ↗
The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is…
Company / brand: Cardinal Health 200 recalls
Official ID Z-3095-2026 · Official record ↗
The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is…
Company / brand: Cardinal Health 200 recalls
Official ID Z-3094-2026 · Official record ↗
Complaints of blue-green discoloration in product
Company / brand: Fresenius Medical Care Renal Therapies Group recalls
Official ID Z-3093-2026 · Official record ↗
Complaints of blue-green discoloration in product
Company / brand: Fresenius Medical Care Renal Therapies Group recalls
Official ID Z-3092-2026 · Official record ↗
Complaints of blue-green discoloration in product
Company / brand: Fresenius Medical Care Renal Therapies Group recalls
Official ID Z-3091-2026 · Official record ↗
Specific lots of Discofix Stopcock Sets recalled due to an incorrect expiration date printed on the carton shipper label.
Company / brand: B Braun Medical recalls
Official ID Z-3089-2026 · Official record ↗
Software issue within robotic controller which may cause unintended movement of the robotic arm during bone preparation or instrument positioning.
Company / brand: Medos International Sarl recalls
Official ID Z-3088-2026 · Official record ↗
Heightened probability of blood leak from the connection between the Arterial Alpha Clip and the main line or pump segment. Leak during treatment may lead to blood loss and hypovol…
Company / brand: Fresenius Medical Care Renal Therapies Group recalls
Official ID Z-3087-2026 · Official record ↗
Heightened probability of blood leak from the connection between the Arterial Alpha Clip and the main line or pump segment. Leak during treatment may lead to blood loss and hypovol…
Company / brand: Fresenius Medical Care Renal Therapies Group recalls
Official ID Z-3086-2026 · Official record ↗
Heightened probability of blood leak from the connection between the Arterial Alpha Clip and the main line or pump segment. Leak during treatment may lead to blood loss and hypovol…
Company / brand: Fresenius Medical Care Renal Therapies Group recalls
Official ID Z-3085-2026 · Official record ↗
Heightened probability of blood leak from the connection between the Arterial Alpha Clip and the main line or pump segment. Leak during treatment may lead to blood loss and hypovol…
Company / brand: Fresenius Medical Care Renal Therapies Group recalls
Official ID Z-3084-2026 · Official record ↗
There is potential for a delay in AF Burden Alert notification affecting the server software which supports the Insertable Cardiac Monitors (ICMs). Delayed notification of an AF Bu…
Company / brand: Boston Scientific recalls
Official ID Z-3083-2026 · Official record ↗
There is potential for a delay in AF Burden Alert notification affecting the server software which supports the Insertable Cardiac Monitors (ICMs). Delayed notification of an AF Bu…
Company / brand: Boston Scientific recalls
Official ID Z-3082-2026 · Official record ↗
There is potential for a delay in AF Burden Alert notification affecting the server software which supports the Insertable Cardiac Monitors (ICMs). Delayed notification of an AF Bu…
Company / brand: Boston Scientific recalls
Official ID Z-3081-2026 · Official record ↗
Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the app…
Company / brand: Medline Industries recalls
Official ID Z-3079-2026 · Official record ↗
Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the app…
Company / brand: Medline Industries recalls
Official ID Z-3078-2026 · Official record ↗
Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the app…
Company / brand: Medline Industries recalls
Official ID Z-3077-2026 · Official record ↗
Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the app…
Company / brand: Medline Industries recalls
Official ID Z-3076-2026 · Official record ↗
Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the app…
Company / brand: Medline Industries recalls
Official ID Z-3075-2026 · Official record ↗
Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the app…
Company / brand: Medline Industries recalls
Official ID Z-3074-2026 · Official record ↗
Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the app…
Company / brand: Medline Industries recalls
Official ID Z-3073-2026 · Official record ↗
Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the app…
Company / brand: Medline Industries recalls
Official ID Z-3072-2026 · Official record ↗
Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the app…
Company / brand: Medline Industries recalls
Official ID Z-3071-2026 · Official record ↗
Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the app…
Company / brand: Medline Industries recalls
Official ID Z-3070-2026 · Official record ↗
Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the app…
Company / brand: Medline Industries recalls
Official ID Z-3069-2026 · Official record ↗
Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the app…
Company / brand: Medline Industries recalls
Official ID Z-3068-2026 · Official record ↗
Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the app…
Company / brand: Medline Industries recalls
Official ID Z-3067-2026 · Official record ↗
A software issue that may occur during a Volume/Time (VOT) multi-syringe infusion when a syringe reaches empty and is replaced while a Volume To Be Infused (VTBI) remains.
Company / brand: Baxter Healthcare recalls
Official ID Z-3066-2026 · Official record ↗
A software issue that may occur during a Volume/Time (VOT) multi-syringe infusion when a syringe reaches empty and is replaced while a Volume To Be Infused (VTBI) remains.
Company / brand: Baxter Healthcare recalls
Official ID Z-3065-2026 · Official record ↗
Surgical instructions sent for viscoelastic products used during ophthalmic viscosurgical cataract procedures including in part: If resistance is encountered during insertion, with…
Company / brand: Johnson & Johnson Surgical Vision recalls
Official ID Z-3064-2026 · Official record ↗
The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in the paper lidding whi…
Company / brand: Medline Industries recalls
Official ID Z-3063-2026 · Official record ↗
The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in the paper lidding whi…
Company / brand: Medline Industries recalls
Official ID Z-3062-2026 · Official record ↗
The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in the paper lidding whi…
Company / brand: Medline Industries recalls
Official ID Z-3061-2026 · Official record ↗
The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in the paper lidding whi…
Company / brand: Medline Industries recalls
Official ID Z-3060-2026 · Official record ↗
The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in the paper lidding whi…
Company / brand: Medline Industries recalls
Official ID Z-3059-2026 · Official record ↗
The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in the paper lidding whi…
Company / brand: Medline Industries recalls
Official ID Z-3058-2026 · Official record ↗
The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in the paper lidding whi…
Company / brand: Medline Industries recalls
Official ID Z-3057-2026 · Official record ↗
The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in the paper lidding whi…
Company / brand: Medline Industries recalls
Official ID Z-3056-2026 · Official record ↗
The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in the paper lidding whi…
Company / brand: Medline Industries recalls
Official ID Z-3055-2026 · Official record ↗
The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in the paper lidding whi…
Company / brand: Medline Industries recalls
Official ID Z-3054-2026 · Official record ↗
The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in the paper lidding whi…
Company / brand: Medline Industries recalls
Official ID Z-3053-2026 · Official record ↗
The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in the paper lidding whi…
Company / brand: Medline Industries recalls
Official ID Z-3052-2026 · Official record ↗
The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in the paper lidding whi…
Company / brand: Medline Industries recalls
Official ID Z-3051-2026 · Official record ↗
The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in the paper lidding whi…
Company / brand: Medline Industries recalls
Official ID Z-3050-2026 · Official record ↗
The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in the paper lidding whi…
Company / brand: Medline Industries recalls
Official ID Z-3049-2026 · Official record ↗
The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in the paper lidding whi…
Company / brand: Medline Industries recalls
Official ID Z-3048-2026 · Official record ↗
A positive drift in QC values within the reagent's stated 4-hour onboard stability period was identified
Company / brand: Diagnostica Stago recalls
Official ID Z-3047-2026 · Official record ↗
The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile Models 55992C to 55998…
Company / brand: AVID Medical recalls
Official ID Z-3046-2026 · Official record ↗
The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile Models 55992C to 55998…
Company / brand: AVID Medical recalls
Official ID Z-3045-2026 · Official record ↗
The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile Models 55992C to 55998…
Company / brand: AVID Medical recalls
Official ID Z-3044-2026 · Official record ↗
Philips has identified an unintended radiation issue with the Philips IQon, iCT, Ingenuity, and Brilliance CT 64 systems that could affect the performance of the equipment.
Company / brand: Philips North America recalls
Official ID Z-3043-2026 · Official record ↗
Philips has identified an unintended radiation issue with the Philips IQon, iCT, Ingenuity, and Brilliance CT 64 systems that could affect the performance of the equipment.
Company / brand: Philips North America recalls
Official ID Z-3042-2026 · Official record ↗
Philips has identified an unintended radiation issue with the Philips IQon, iCT, Ingenuity, and Brilliance CT 64 systems that could affect the performance of the equipment.
Company / brand: Philips North America recalls
Official ID Z-3041-2026 · Official record ↗
Philips has identified an unintended radiation issue with the Philips IQon, iCT, Ingenuity, and Brilliance CT 64 systems that could affect the performance of the equipment.
Company / brand: Philips North America recalls
Official ID Z-3040-2026 · Official record ↗
Undeclared milk.
Company / brand: Fayus recalls
Official ID H-1329-2026 · Official record ↗
Product tested positive for undeclared milk.
Company / brand: Marina Del Rey Foods recalls
Official ID H-1328-2026 · Official record ↗
Foreign object: metal fragments
Company / brand: Ukrop's Homestyle Foods recalls
Official ID H-1327-2026 · Official record ↗
Foreign object: metal fragments
Company / brand: Ukrop's Homestyle Foods recalls
Official ID H-1326-2026 · Official record ↗
Undeclared FD&C Red No. 40
Company / brand: Wonton Specialists recalls
Official ID H-1325-2026 · Official record ↗
Undeclared FD&C Red No. 40
Company / brand: Wonton Specialists recalls
Official ID H-1324-2026 · Official record ↗
Undeclared FD&C Red No. 40
Company / brand: Wonton Specialists recalls
Official ID H-1323-2026 · Official record ↗
Undeclared FD&C Red No. 40
Company / brand: Wonton Specialists recalls
Official ID H-1322-2026 · Official record ↗
Undeclared FD&C Red No. 40
Company / brand: Wonton Specialists recalls
Official ID H-1321-2026 · Official record ↗
Undeclared FD&C Red No. 40
Company / brand: Wonton Specialists recalls
Official ID H-1320-2026 · Official record ↗
Product tested positive for undeclared milk allergen.
Company / brand: Savor Seasonings recalls
Official ID H-1319-2026 · Official record ↗
Product may be contaminated with Salmonella.
Company / brand: THE HAMPTON GROCER recalls
Official ID H-1309-2026 · Official record ↗
Product has high patulin levels
Company / brand: WEIS MARKETS recalls
Official ID H-1308-2026 · Official record ↗
Milk is not declared in the Contains statement.
Company / brand: Prince Bakery recalls
Official ID H-1307-2026 · Official record ↗
Sesame is not declared in the ingredient statement but is declared in the statement of identity.
Company / brand: Prince Bakery recalls
Official ID H-1306-2026 · Official record ↗
Sesame is not declared in the ingredient statement but is declared in the statement of identity.
Company / brand: Prince Bakery recalls
Official ID H-1305-2026 · Official record ↗
Sesame is not declared in the ingredient statement but is declared in the statement of identity.
Company / brand: Prince Bakery recalls
Official ID H-1304-2026 · Official record ↗
Products were manufactured with jalapenos that have the potential to be contaminated with Salmonella
Company / brand: Ron's Home Style Foods recalls
Official ID H-1303-2026 · Official record ↗
Products were manufactured with jalapenos that have the potential to be contaminated with Salmonella
Company / brand: Ron's Home Style Foods recalls
Official ID H-1302-2026 · Official record ↗
Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin.
Company / brand: OPTIMAL BALANCE PHARMACY recalls
Official ID D-0851-2026 · Official record ↗
Presence of particulate matter: Particulates identified as fiberglass
Company / brand: Baxter Healthcare recalls
Official ID D-0849-2026 · Official record ↗
Failed Dissolution Specifications. Notification from the manufacturer that lot is being recalled due to failed dissolution
Company / brand: Golden State Medical Supply recalls
Official ID D-0847-2026 · Official record ↗
Labeling: Label Mix-up
Company / brand: American Health Packaging recalls
Official ID D-0840-2026 · Official record ↗
Failed Dissolution Specifications; product failed to meet 18-month stability testing acceptance criteria
Company / brand: Mylan Pharmaceuticals recalls
Official ID D-0839-2026 · Official record ↗
Failed Stability Specifications: Out of specification stability result for the protein concentration profile.
Company / brand: Chiesi USA recalls
Official ID D-0838-2026 · Official record ↗
Cross Contamination with Other Products
Company / brand: Sage Products recalls
Official ID D-0837-2026 · Official record ↗
Presence of Foreign Tablets/Capsules
Company / brand: Teva Pharmaceuticals USA recalls
Official ID D-0834-2026 · Official record ↗
Failed dissolution specifications.
Company / brand: Supernus Pharmaceuticals recalls
Official ID D-0833-2026 · Official record ↗
Failed Dissolution Specifications
Company / brand: Mylan Pharmaceuticals recalls
Official ID D-0830-2026 · Official record ↗
CGMP Deviations: Potential contamination of raw material
Company / brand: Lexia recalls
Official ID D-0829-2026 · Official record ↗
CGMP Deviations: Potential contamination of raw material
Company / brand: Lexia recalls
Official ID D-0828-2026 · Official record ↗
Subpotent Product: Firm Testing indicated the affected product may not reliably provide the SPF 50 protection stated on the label.
Company / brand: Allies Group recalls
Official ID D-0826-2026 · Official record ↗
Subpotent Product: Firm Testing indicated the affected product may not reliably provide the SPF 50 protection stated on the label.
Company / brand: Allies Group recalls
Official ID D-0825-2026 · Official record ↗
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Government sources last checked October 22, 2026 at 12:00 PM UTC.