Vereinigte Staaten Recalls

Verbraucherrückrufe von FDA, CPSC, NHTSA und USDA FSIS.

Showing 24 of 17,562 results
Food & BeverageUSFDA Food

UPC 21914600000 KITCHEN SANDWICH CROISSANT CHICKEN CASHEW SS This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.

Albertsons Companies LLC
FDA FoodClass III

UPC 21914600000 KITCHEN SANDWICH CROISSANT CHICKEN CASHEW SS This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.

Contains statement does not declare Cashew

Jun 10, 2026Albertsons Companies LLC
Food & BeverageUSFDA Food

UPC 21495100000 Ready Meals MEAL SALMON CAJUN SS COLD This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.

Albertsons Companies LLC
FDA FoodClass III

UPC 21495100000 Ready Meals MEAL SALMON CAJUN SS COLD This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.

Contains statement does not declare Salmon

Jun 10, 2026Albertsons Companies LLC
Food & BeverageUSFDA Food

UPC 25139500000 Cake Cakerie Strawberry Shortcake Triangle. This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.

Albertsons Companies LLC
FDA FoodClass II

UPC 25139500000 Cake Cakerie Strawberry Shortcake Triangle. This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.

Contains statement does not declare Hazelnut.

Jun 10, 2026Albertsons Companies LLC
Food & BeverageUSFDA Food

UPC 23098000000 SALMON ATLANTIC PORTION CA ORANGE MARINADE This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.

Albertsons Companies LLC
FDA FoodClass III

UPC 23098000000 SALMON ATLANTIC PORTION CA ORANGE MARINADE This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.

Contains statement does not declare Salmon

Jun 10, 2026Albertsons Companies LLC
Food & BeverageUSFDA Food

UPC 28994500000 PAVILIONS MUFFINS BANANA NUT SINGLE SERVE This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.

Albertsons Companies LLC
FDA FoodClass II

UPC 28994500000 PAVILIONS MUFFINS BANANA NUT SINGLE SERVE This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.

Contains statement does not declare Walnut

Jun 10, 2026Albertsons Companies LLC
Food & BeverageUSFDA Food

UPC 23285600000 IMITATION CRAB AND SHRIMP SALAD SRIRACHA This is Albertson's store-made item and sold by random weight at point of sale with grocery store's scale label.

Albertsons Companies LLC
FDA FoodClass II

UPC 23285600000 IMITATION CRAB AND SHRIMP SALAD SRIRACHA This is Albertson's store-made item and sold by random weight at point of sale with grocery store's scale label.

Contains statement does not declare Pollock

Jun 10, 2026Albertsons Companies LLC
Food & BeverageUSFDA Food

UPC 29132100000 KITCHEN SNACKER SALAD TUNA PICKLE This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.

Albertsons Companies LLC
FDA FoodClass III

UPC 29132100000 KITCHEN SNACKER SALAD TUNA PICKLE This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.

Contains statement does not declare Tuna

Jun 10, 2026Albertsons Companies LLC
Food & BeverageUSFDA Food

UPC 24512800000 SALAD CHICKEN CAESAR UPC 29854600000 Kitchen SALAD CHICKEN CAESAR This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.

Albertsons Companies LLC
FDA FoodClass II

UPC 24512800000 SALAD CHICKEN CAESAR UPC 29854600000 Kitchen SALAD CHICKEN CAESAR This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.

Contains statement does not declare Anchovy

Jun 10, 2026Albertsons Companies LLC
Medical DeviceUSFDA Devices

Brand Name: B. BRAUN MEDICAL INC. Product Name: SESK UPMC DOUBLE CATHETER TRAY Model/Catalog Number: 530134 Software Version: N/A Product Description: SESK UPMC DOUBLE CATHETER TRAY Component: No

B Braun Medical Inc
FDA DevicesClass II

Brand Name: B. BRAUN MEDICAL INC. Product Name: SESK UPMC DOUBLE CATHETER TRAY Model/Catalog Number: 530134 Software Version: N/A Product Description: SESK UPMC DOUBLE CATHETER TRAY Component: No

B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential cracking of the butyrate tubing (outside tube), which renders the product unusable.

Jun 10, 2026B Braun Medical Inc
Medical DeviceUSFDA Devices

Philips Azurion 5M12, Model Numbers: 722227 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
FDA DevicesClass II

Philips Azurion 5M12, Model Numbers: 722227 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key

During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly touching the footswitch pedal without generating an Xray image). The pedal tap may cause a dark image with the next fluoroscopy run.

Jun 10, 2026PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Food & BeverageUSFDA Food

Cold Prep Cream Sauce, 20 lb., packaged in a tied poly bag and packed 1 bag per case, UPC 0039954922458

The Coffee Connexion Co., Inc
FDA FoodClass I

Cold Prep Cream Sauce, 20 lb., packaged in a tied poly bag and packed 1 bag per case, UPC 0039954922458

Product contains dry milk powder ingredient recalled by the supplier due to potential Salmonella contamination

Jun 10, 2026The Coffee Connexion Co., Inc
Medical DeviceUSFDA Devices

Design Options Spinal Tray Spinal Needle Anesthesia procedure kits: Material Description (Material Number): SSK H M C 20061890 (560074), SSK S C H (560214), SSK BJC H S (ORIGINAL CUST) (560272), SSK CA P M C (ORIGINAL CUST) (560327), SSK T M H (560394), SSK S O 20070208 (560428), SSK L G H (ORIGINAL CUST) (560462), SSK H M H (560465), SSK BUPIVACAINE TRAY 2068824 (560476), SSK K F H (560497), SSK T J U H (560513), SSK O M C (560521), SSK CUSTOM SPINAL TRAY (560523), SSK O R M C (560533), SSK B S H S 20115122 (560538), SSK M M (560572), SSK M S 27GA PENCAN SPINAL TRAY (560580), SSK S T H & C (560584), SSK U C (560587), SSK P25BKG (560603), SSK P24BKG (560606), SSK S25BKG (560607), SSK M C - BUPIVACAINE TRAY (560609), SSK T M C (560613), SSK PENCIL POINT SPINAL TRAY (560619), SSK E O & S H-SPINAL (560621), SSK BSW SPINAL TRAY (560628), SSK M C OB DEPT - SPINAL (560645), SSK B H M (560646), SSK M G M C (560647), SSK S M H (560648), SSK H H S (560660), O S U M C SPINAL TRAY SSK (560667), A M C, SSK (560670), S B H - SPINAL TRAY SSK (560672);

B Braun Medical Inc
FDA DevicesClass I

Design Options Spinal Tray Spinal Needle Anesthesia procedure kits: Material Description (Material Number): SSK H M C 20061890 (560074), SSK S C H (560214), SSK BJC H S (ORIGINAL CUST) (560272), SSK CA P M C (ORIGINAL CUST) (560327), SSK T M H (560394), SSK S O 20070208 (560428), SSK L G H (ORIGINAL CUST) (560462), SSK H M H (560465), SSK BUPIVACAINE TRAY 2068824 (560476), SSK K F H (560497), SSK T J U H (560513), SSK O M C (560521), SSK CUSTOM SPINAL TRAY (560523), SSK O R M C (560533), SSK B S H S 20115122 (560538), SSK M M (560572), SSK M S 27GA PENCAN SPINAL TRAY (560580), SSK S T H & C (560584), SSK U C (560587), SSK P25BKG (560603), SSK P24BKG (560606), SSK S25BKG (560607), SSK M C - BUPIVACAINE TRAY (560609), SSK T M C (560613), SSK PENCIL POINT SPINAL TRAY (560619), SSK E O & S H-SPINAL (560621), SSK BSW SPINAL TRAY (560628), SSK M C OB DEPT - SPINAL (560645), SSK B H M (560646), SSK M G M C (560647), SSK S M H (560648), SSK H H S (560660), O S U M C SPINAL TRAY SSK (560667), A M C, SSK (560670), S B H - SPINAL TRAY SSK (560672);

These procedure kits contain Bupivacaine Hydrochloride in Dextrose Injection, USP. The manufacturer of the Bupivacaine, Huon Co, Ltd., has issued a voluntary recall due to potential quality issues identified during a recent FDA manufacturing facility inspection.

Jun 10, 2026B Braun Medical Inc
Medical DeviceUSFDA Devices

Brand Name: Exacta Mix Product Name: Vented Micro-Volume Inlet Model/Catalog Number: H938175 Product Description: Tubing sets with push-on connector on one end (to attach to the Fluid Selector Valve) and a spike or other appropriate connector on the opposite end to attach the source container.

Baxter Healthcare Corporation
FDA DevicesClass II

Brand Name: Exacta Mix Product Name: Vented Micro-Volume Inlet Model/Catalog Number: H938175 Product Description: Tubing sets with push-on connector on one end (to attach to the Fluid Selector Valve) and a spike or other appropriate connector on the opposite end to attach the source container.

Affected lots may contain incorrect 0.8-micron filters. Use of a 0.8-micron filter in place of the validated 3-micron filter may lead to reduced flow efficiency, incomplete or slower transfers of ingredients, or system alarms. This issue may lead to clinical effects such as electrolyte imbalance, metabolic instability, delayed recovery, etc.

Jun 10, 2026Baxter Healthcare Corporation
Food & BeverageUSFDA Food

UPC 21292200000 SALMON CAJUN PREMIUM FS COLD This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.

Albertsons Companies LLC
FDA FoodClass III

UPC 21292200000 SALMON CAJUN PREMIUM FS COLD This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.

Contains statement does not declare Salmon

Jun 10, 2026Albertsons Companies LLC
PharmaceuticalUSFDA Drugs

Amlodipine and Olmesartan Medoxomil Tablets, 5mg/40mg, Rx Only, 30-count bottle, Manufactured by: Alkem Laboratories Ltd., India, Distributed by: Ascend Laboratories, LLC., Parsippany, NJ 07054, NDC 67877-501-30.

Ascend Laboratories, LLC
FDA DrugsClass II

Amlodipine and Olmesartan Medoxomil Tablets, 5mg/40mg, Rx Only, 30-count bottle, Manufactured by: Alkem Laboratories Ltd., India, Distributed by: Ascend Laboratories, LLC., Parsippany, NJ 07054, NDC 67877-501-30.

Failed Dissolution Specifications: Olmesartan Medoxomil content below specifications

Jun 10, 2026Ascend Laboratories, LLC
Food & BeverageUSFDA Food

Alfredo Sauce, 3 lb. 7 oz., packaged in a sealed poly bag and packed 12 bags per case, UPC 0039954921963

The Coffee Connexion Co., Inc
FDA FoodClass I

Alfredo Sauce, 3 lb. 7 oz., packaged in a sealed poly bag and packed 12 bags per case, UPC 0039954921963

Product contains dry milk powder ingredient recalled by the supplier due to potential Salmonella contamination

Jun 10, 2026The Coffee Connexion Co., Inc
Food & BeverageUSFDA Food

UPC 29153000000 SAMPLER TRAY ITALIAN 16 INCH This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.

Albertsons Companies LLC
FDA FoodClass II

UPC 29153000000 SAMPLER TRAY ITALIAN 16 INCH This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.

Contains statement does not declare Almond

Jun 10, 2026Albertsons Companies LLC
Food & BeverageUSFDA Food

UPC 29604300000 SALMON WASABI GRILLED FS COLD This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.

Albertsons Companies LLC
FDA FoodClass III

UPC 29604300000 SALMON WASABI GRILLED FS COLD This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.

Contains statement does not declare Salmon

Jun 10, 2026Albertsons Companies LLC
PharmaceuticalUSFDA Drugs

GOODSENSE Ultra Strength, Antacid TABLETS, Calcium Carbonate 1000 mg, 72 Chewable Tablets, Distributed by: Geiss, Destin & Dunn, inc., Peachtree City, GA, NDC 50804-171-68.

Guardian Drug Co. Inc.
FDA DrugsClass II

GOODSENSE Ultra Strength, Antacid TABLETS, Calcium Carbonate 1000 mg, 72 Chewable Tablets, Distributed by: Geiss, Destin & Dunn, inc., Peachtree City, GA, NDC 50804-171-68.

Presence of foreign substance: small metallic particles in chewable tablets.

Jun 10, 2026Guardian Drug Co. Inc.
Medical DeviceUSFDA Devices

Spinocan Spinal Needle procedure kits: Material Description (Material Number): Spinocan 26 Ga. x 3-1/2 in. (90 mm), Bupivacaine 0.75% with Dextrose 8.25% Tray (Kit) (333201); Spinocan 25 Ga. x 3-1/2 in. (90 mm), Bupivacaine 0.75% with Dextrose 8.25% Tray (Kit) (333211); Spinocan 22 Ga. x 3-1/2 in. (90 mm), Bupivacaine 0.75% with Dextrose 8.25% Tray (Kit) (333231)

B Braun Medical Inc
FDA DevicesClass I

Spinocan Spinal Needle procedure kits: Material Description (Material Number): Spinocan 26 Ga. x 3-1/2 in. (90 mm), Bupivacaine 0.75% with Dextrose 8.25% Tray (Kit) (333201); Spinocan 25 Ga. x 3-1/2 in. (90 mm), Bupivacaine 0.75% with Dextrose 8.25% Tray (Kit) (333211); Spinocan 22 Ga. x 3-1/2 in. (90 mm), Bupivacaine 0.75% with Dextrose 8.25% Tray (Kit) (333231)

These procedure kits contain Bupivacaine Hydrochloride in Dextrose Injection, USP. The manufacturer of the Bupivacaine, Huon Co, Ltd., has issued a voluntary recall due to potential quality issues identified during a recent FDA manufacturing facility inspection.

Jun 10, 2026B Braun Medical Inc
PharmaceuticalUSFDA Drugs

GOODSENSE Extra Strength, Antacid TABLETS, Calcium Carbonate 750 mg, 96 Chewable Tablets, Distributed by: Geiss, Destin & Dunn, inc., Peachtree City, GA, NDC 50804-129-22.

Guardian Drug Co. Inc.
FDA DrugsClass II

GOODSENSE Extra Strength, Antacid TABLETS, Calcium Carbonate 750 mg, 96 Chewable Tablets, Distributed by: Geiss, Destin & Dunn, inc., Peachtree City, GA, NDC 50804-129-22.

Presence of foreign substance: small metallic particles in chewable tablets.

Jun 10, 2026Guardian Drug Co. Inc.
Vehicle RecallUSNHTSA

Ford Motor Company - Window Automatic Reversal System Malfunction/FMVSS 118

Ford Motor Company
NHTSAVISIBILITY

Ford Motor Company - Window Automatic Reversal System Malfunction/FMVSS 118

A closing window that does not reverse direction as expected can pinch a driver or passenger before retracting, increasing the risk of injury.

Jun 9, 2026Ford Motor Company
Vehicle RecallUSNHTSA

Ford Motor Company - Instrument Cluster Failure/FMVSS 102

Ford Motor Company
NHTSAELECTRICAL SYSTEM

Ford Motor Company - Instrument Cluster Failure/FMVSS 102

An instrument cluster that fails to display critical safety information, such as gear position or warning lights, increases the risk of a crash or injury.

Jun 9, 2026Ford Motor Company
Vehicle RecallUSNHTSA

Ford Motor Company - Vehicle Rollaway Risk

Ford Motor Company
NHTSAPOWER TRAIN

Ford Motor Company - Vehicle Rollaway Risk

A park system that is damaged may not shift into "PARK," resulting in a vehicle rollaway and increasing the risk of injury or crash.

Jun 9, 2026Ford Motor Company

Install The Recall File App

Check safety warnings, scan your pantry, and monitor your vehicles directly from your home screen.