Safety Recalls

15,200 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.

Showing 4,301–4,350 of 15,200

• Food Recall · September 20, 2025

  Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

  Kroger Mercado Cooked Medium Peeled Tail-Off Shrimp, net wt. 2lbs. UPC 011110626196. Product is packaged in clear plastic bag and has a white label with green stripes on top of each bag.

  Shrimp may be contaminated with Cesium-137 (Cs-137).

  Class II

• Food Recall · September 20, 2025

  Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

  AquaStar 16/20 Frozen Raw EZ-Peel White Shrimp, net wt. 5 lbs. UPC 731149654075. Product was sold at WinCo.

  Shrimp may be contaminated with Cesium-137 (Cs-137).

  Class II

• Food Recall · September 20, 2025

  Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

  Waterfront Bistro Frozen Raw EZ-Peel White Shrimp 21/25, net wt. 2lbs., UPC 021130123223. Product was sold at Shaw s and Star Market, Albertson's, Eagle, Carrs-Safeway, and Safeway.

  Shrimp may be contaminated with Cesium-137 (Cs-137).

  Class II

• Food Recall · September 20, 2025

  Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

  Kroger Raw Colossal EZ Peel Shrimp, net wt. 2lbs., UPC 20011110643906. Product is packaged in transparent printed bag with a blue band on the top with yellow and red details.

  Shrimp may be contaminated with Cesium-137 (Cs-137).

  Class II

• Food Recall · September 20, 2025

  Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

  AquaStar Raw Peeled Tail-on Shrimp Skewers, net wt. 1.25lbs. UPC 731149390010. Product is packaged in a printed bag with a black top and blue bottom and printed pictures of the skewers inside.

  Shrimp may be contaminated with Cesium-137 (Cs-137).

  Class II

• Food Recall · September 20, 2025

  Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

  AquaStar 13/15 Raw Shrimp Easy Peel Deveined, net wt. 2 lbs. UPC 731149654051. Product was sold at Publix.

  Shrimp may be contaminated with Cesium-137 (Cs-137).

  Class II

• Food Recall · September 20, 2025

  Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

  Publix Extra Large Shrimp Easy to Peel Deveined 21/25, net wt. 1.5 lbs. UPC 041415064454. Product was sold at Publix.

  Shrimp may be contaminated with Cesium-137 (Cs-137).

  Class II

• Food Recall · September 20, 2025

  Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

  Best Yet Frozen Raw EZ-Peel White Shrimp 16/20 (net wt. 1 lbs/pkg; 10 pkgs per case). UPC 04218700282 Best Yet Frozen Raw EZ-Peel White Shrimp 21/25 (net wt. 1 lbs/pkg; 10 pkgs per case). UPC 04218

  Shrimp may be contaminated with Cesium-137 (Cs-137).

  Class II

• Food Recall · September 20, 2025

  Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

  Publix Large Shrimp Peeled & Deveined Tail On 31/40, net wt. 1.5 lbs. UPC 041415067455. Product was sold at Publix.

  Shrimp may be contaminated with Cesium-137 (Cs-137).

  Class II

• Food Recall · September 19, 2025

  Black Sheep Egg Company, LLC

  Free Range Grade A Large Brown Eggs, 12ct Cartons, UPC: 860010568507, Black Sheep Egg Company 400 S Memorial Drive Walnut Ridge AR 72476

  Potential Salmonella contamination.

  Class I

• Medical Device Recall · September 19, 2025

  Beckman Coulter, Inc.

  DxC 500i Clinical Analyzer Modules, DxC 500 AU Module w/ISE, DxC 500i (Part Number C63522), DxC 500 AU Module, DxC 500i (Part Number C63521), and Access 2 Module, DxC 500i (Part Number C13252)

  Beckman Coulter has confirmed a software anomaly on DxI 9000 Access Immunoassay Analyzer and the DxC 500i Clinical Analyzer that may prevent correct application of user-specified manual dilution factors when ordering additional tests for samples already "In Progress" using the same "Sample ID number". This can lead to false low or high patient results and potential delays in reporting, risking erroneous diagnoses if undetected.

  Class II

• Food Recall · September 19, 2025

  Black Sheep Egg Company, LLC

  Free Range Grade AA Medium White Eggs, Loose Open Skid, 900dz per pallet, Black Sheep Egg Company 400 S Memorial Drive Walnut Ridge AR 72476

  Potential Salmonella contamination.

  Class I

• Medical Device Recall · September 19, 2025

  Orthofix U.S. LLC

  Virata Preassembled Polyaxial Screw, utilized in the Virata Spinal Fixation System. The following sizes are affected: 1. POLYAXIAL SCREW, CC, 5.5mm X 30mm; Item Number: TL1-10755030. 2. POLYAXI

  Polyaxial screws do not meet performance standards.

  Class II

• Drug Recall · September 19, 2025

  Ascend Laboratories, LLC

  Atorvastatin Calcium Tablets USP, 80 mg, Rx Only, a). 90-count(NDC 67877-514-90), b). 500-count(NDC 67877-514-05), Manufactured by: Alkem Laboratories, Ltd. India, Distributed by: Ascend Laboratories,

  Failed Dissolution Specifications

  Class II

• Food Recall · September 19, 2025

  Black Sheep Egg Company, LLC

  Free Range Grade AA Large Brown Eggs, Loose Pack in Boxes, 15dz per box, Black Sheep Egg Company 400 S Memorial Drive Walnut Ridge AR 72476

  Potential Salmonella contamination.

  Class I

• Drug Recall · September 19, 2025

  Ascend Laboratories, LLC

  Atorvastatin Calcium Tablets USP, 40 mg, Rx Only, a). 90-count (NDC 67877-513-90), b). 500-count (NDC 67877-513-05), c). 1000-count (NDC 67877-513-10), Manufactured by: Alkem Laboratories, Ltd. Ind

  Failed Dissolution Specifications

  Class II

• Food Recall · September 19, 2025

  Black Sheep Egg Company, LLC

  Free Range Grade AA Medium Brown Eggs, Loose Pack in Boxes, 15dz per box, Black Sheep Egg Company 400 S Memorial Drive Walnut Ridge AR 72476

  Potential Salmonella contamination.

  Class I

• Food Recall · September 19, 2025

  Black Sheep Egg Company, LLC

  Free Range Grade AA Medium White Eggs, 18ct Cartons, 15dz per box, Black Sheep Egg Company 400 S Memorial Drive Walnut Ridge AR 72476

  Potential Salmonella contamination.

  Class I

• Drug Recall · September 19, 2025

  Ascend Laboratories, LLC

  Atorvastatin Calcium Tablets USP, 10 mg, Rx Only a) 90-count bottle (NDC 67877-511-90), b). 500-count bottle (NDC 67877-511-05), c). 1000-count bottle (NDC 67877-511-10) Manufactured by: Alkem Laborat

  Failed Dissolution Specifications

  Class II

• Food Recall · September 19, 2025

  Black Sheep Egg Company, LLC

  Free Range Grade AA Large White Eggs, 12ct Cartons, 15dz per box, Black Sheep Egg Company 400 S Memorial Drive Walnut Ridge AR 72476

  Potential Salmonella contamination.

  Class I

• Food Recall · September 19, 2025

  Black Sheep Egg Company, LLC

  Free Range Grade AA Large Brown Eggs, Loose Open Skid, 900dz per pallet, Black Sheep Egg Company 400 S Memorial Drive Walnut Ridge AR 72476

  Potential Salmonella contamination.

  Class I

• Drug Recall · September 19, 2025

  Ascend Laboratories, LLC

  Atorvastatin Calcium Tablets USP, 20 mg, Rx Only, a). 90-count(NDC 67877-512-90), b). 500-count (NDC 67877-512-05), c). 1000-count(NDC 67877-512-10),Manufactured by: Alkem Laboratories, Ltd. India, D

  Failed Dissolution Specifications

  Class II

• Food Recall · September 19, 2025

  Black Sheep Egg Company, LLC

  Free Range Grade AA Medium Brown Eggs, Loose Open Skid, 900dz per pallet, Black Sheep Egg Company 400 S Memorial Drive Walnut Ridge AR 72476

  Potential Salmonella contamination.

  Class I

• Food Recall · September 19, 2025

  Black Sheep Egg Company, LLC

  Free Range Grade AA Large White Eggs, Loose Open Skid, 900dz per pallet, Black Sheep Egg Company 400 S Memorial Drive Walnut Ridge AR 72476

  Potential Salmonella contamination.

  Class I

• Food Recall · September 19, 2025

  Black Sheep Egg Company, LLC

  Free Range Grade A Large Brown Eggs, 18ct Cartons, UPC: 860010568538, Black Sheep Egg Company 400 S Memorial Drive Walnut Ridge AR 72476

  Potential Salmonella contamination.

  Class I

• Medical Device Recall · September 19, 2025

  Kico Knee Innovation Company

  Brand Name: ARVIS Product Name: ARVIS" Shoulder Model/Catalog Number: IN-27300, Arvis Surgical Planning Software Software Version: V2025.1.2 Product Description: Intended Use: The ARVIS" system is

  Complaint identified issue with AI surgical planning software that may result in implant malalignment and/or decrease range of motion.

  Class II

• Medical Device Recall · September 19, 2025

  Beckman Coulter, Inc.

  DxI 9000 Access Immunoassay Analyzer, Part Number C11137

  Beckman Coulter has confirmed a software anomaly on DxI 9000 Access Immunoassay Analyzer and the DxC 500i Clinical Analyzer that may prevent correct application of user-specified manual dilution factors when ordering additional tests for samples already "In Progress" using the same "Sample ID number". This can lead to false low or high patient results and potential delays in reporting, risking erroneous diagnoses if undetected.

  Class II

• Food Recall · September 18, 2025

  Egress Capital Partners Inc.

  Taproom Gourmet brand 20lb and 18lb bulk "Fifth Avenue" Mix

  No ingredient label. Product contains undeclared allergens (peanuts, almonds, cashew, and soy)

  Class II

• Food Recall · September 18, 2025

  Egress Capital Partners Inc.

  Taproom Gourmet brand 15lb bulk "Madison" Mix

  No ingredient label. Product contains undeclared allergens (peanuts, almonds, wheat, and soy)

  Class II

• Food Recall · September 18, 2025

  Western United Fish Company Inc

  Kirkland Signature brand Ahi Tuna Wasabi Poke, Costco #17193, net wt. 1lb. Product is packaged in clear plastic clamshell container and sold to consumers.

  Listeria monocytogenes. Recall was initiated after being notified by green onion supplier of a Listeria monocytogenes positive test result in the green onions which were used only in Ahi Tuna Wasabi Poke.

  Class I

• Food Recall · September 18, 2025

  Egress Capital Partners Inc.

  Taproom Gourmet brand 15lb bulk "Broadway" Mix

  No ingredient label. Product contains undeclared allergens (peanuts, sesame, wheat, and soy)

  Class II

• Food Recall · September 18, 2025

  Goyal Group Inc.

  1. SILVER HORSE - PURE ALUMINIUM MADE IN INDIA - ALUMINIUM MILK PAN 4 inches 2. SILVER HORSE - ALUMINIUM MATHAR KADAI - 26 inches

  Contains elevated levels of lead

  Class II

• Medical Device Recall · September 18, 2025

  B BRAUN MEDICAL INC

  Combined Spinal and Epidural Anesthesia Tray, PERIFIX 17 Ga. x 3-1/2 in. (8.9 cm) Tuohy Epidural Needle, PENCAN 27 Ga. x 5 in. (12.7 cm) Spinal Needle and 19 Ga. Open Tip PERIFIX FX Springwound Epidur

  Potential for the lid of the catheter connector to be in the incorrect position.

  Class II

• Medical Device Recall · September 18, 2025

  Abbott Laboratories

  Brand Name: Alinity hq Analyzer Product Name: Alinity hq Analyzer Model/Catalog Number: 09P68-01 Software Version: 5.0 to 5.10.1 for OUS, 5.7 and 5.10.1 in the US Product Description: Alinity hq A

  Software issue for hq analyzer results in system not visibly applying appropriate flagging to results when saturation is present which may result in incorrect results.

  Class II

• Medical Device Recall · September 18, 2025

  B BRAUN MEDICAL INC

  Design Options, PERIFIX FX Epidural Anesthesia Tray. Product Code: CESK. Product Descriptions: 1. CESK ROBERT WOOD JOHNSON UNIV HOSP. 2. CESK EAST JEFFERSON GEN HOSP 20071769. 3. CESK FLET

  Potential for the lid of the catheter connector to be in the incorrect position.

  Class II

• Consumer Product Recall · September 18, 2025

  IcyBreeze Cooling LLC, of Grapevine, Texas

  IcyBreeze Buddy Portable Misting Fans

  The misting fan can overheat while charging and ignite, posing a fire hazard.

  Unclassified

• Consumer Product Recall · September 18, 2025

  Yiwu Shi Yuxing Keji Youxiangongsi, dba YooxArmor, of China

  YooxArmor Multi-Purpose Kids' Helmets

  The recalled kids' helmets violate the mandatory safety standard for bicycle helmets because the helmets do not comply with the impact attenuation, positional stability, labeling and certification requirements. The helmets can fail to protect the user in the event of a crash, posing a serious risk of injury or death due to head injury.

  Unclassified

• Medical Device Recall · September 18, 2025

  B BRAUN MEDICAL INC

  PERIFIX FX Continuous Epidural Anesthesia Tray, PERIFIX 17 Ga. x 3-1/2 in. (8.9 cm) Tuohy Epidural Needle - Winged and 19 Ga. Closed tip PERIFIX FX Springwound Epidural Catheter. Product Code: CE17TKF

  Potential for the lid of the catheter connector to be in the incorrect position.

  Class II

• Medical Device Recall · September 18, 2025

  B BRAUN MEDICAL INC

  Combined Spinal and Epidural Anesthesia Tray 2, PERIFIX 17 Ga. x 3-1/2 in. (8.9 cm) Tuohy Epidural Needle, PENCAN 27 Ga. x 5 in. (12.7 cm) Spinal Needle, and 19 Ga. Closed Tip PERIFIX FX Springwound E

  Potential for the lid of the catheter connector to be in the incorrect position.

  Class II

• Medical Device Recall · September 18, 2025

  Cardinal Health 200, LLC

  Salem Sump PVC Tubes: Product Code/Product Name: 8888265108 Salem Sump Silicone Dual Lumen Stomach Tube, Radiopaque Line, 10 Fr/Ch (3.3 mm), 36 (91 cm) 8888265116 Salem Sump Silicone Dual Lumen

  Firm has received complaints regarding Anti-Reflux Valve (ARV) breakage due to excessive force during use. Firm is providing additional guidance for use. Expansion of RES 95214.

  Class II

• Medical Device Recall · September 18, 2025

  GE Medical Systems, LLC

  LOGIQ P10 series with software version R4.5.7 Model Number 5877534

  The Ultrasound-Guided Attenuation Parameter (UGAP) measurement data may display inaccurate values representing liver steatosis. This could potentially lead to inappropriate clinical decisions impacting overall care.

  Class II

• Medical Device Recall · September 18, 2025

  B BRAUN MEDICAL INC

  PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. x 3-1/2 in. (8.9cm) Tuohy Epidural Needle - Winged and 19 Ga. Closed tip PERIFIX FX Springwound Epidural Catheter. Product Code: CE17

  Potential for the lid of the catheter connector to be in the incorrect position.

  Class II

• Medical Device Recall · September 18, 2025

  Cardinal Health 200, LLC

  Salem Sump PVC Tubes: Product Code/Product Name: 264929 Salem Sump" Stomach Tube, Dual Lumen, 12 Fr/Ch (4.0 mm) 264945 Salem Sump" Stomach Tube, Dual Lumen, 14 Fr/Ch (4.7 mm) 264960 Salem Sump"

  Firm has received complaints regarding Anti-Reflux Valve (ARV) breakage due to excessive force during use. Firm is providing additional guidance for use. Expansion of RES 95214.

  Class II

• Food Recall · September 18, 2025

  Egress Capital Partners Inc.

  Taproom Gourmet brand 20lb bulk "Park" Mix

  No ingredient label. Product contains undeclared allergens (peanuts, almonds, cashews, wheat, soy, and sesame)

  Class II

• Medical Device Recall · September 18, 2025

  B BRAUN MEDICAL INC

  PERIFIX FX Continuous Epidural Anesthesia Tray, 17 Ga. x 3-1/2 in. (8.9 cm) Tuohy Epidural Needle - Fixed Wings, 19 Ga. Open tip PERIFIX FX Springwound Epidural Catheter. Product Code: CE17TKFSDT. Pro

  Potential for the lid of the catheter connector to be in the incorrect position.

  Class II

• Medical Device Recall · September 18, 2025

  HeartSine Technologies Ltd

  HeartSine Pad-Pak, REF: PAD-PAK-01, PAD-PAK-02, PAD-PAK-03, PAD-PAK-04, PAD-PAK-07, PAD-PAK-03J, PAD-PAK-04J

  Due to customer complaints, defibrillator pads may contain damage pins that disrupt the mechanical fit and electrical contact.

  Class II

• Food Recall · September 18, 2025

  Egress Capital Partners Inc.

  Taproom Gourmet brand 18lb bulk "Empire" Mix

  No ingredient label. Product contains undeclared allergens (cashews, almonds, walnuts, Brazil nuts, pecans, pistachios)

  Class II

• Medical Device Recall · September 18, 2025

  B BRAUN MEDICAL INC

  PERIFIX FX Continuous Epidural Anesthesia Set, PERIFIX Tuohy Epidural Needle - 17 Ga. x 3-1/2 in. (8.9 cm) - Winged, PERIFIX FX Springwound Epidural Catheter - 19 Ga. Closed tip. Product Code: CE17TFC

  Potential for the lid of the catheter connector to be in the incorrect position.

  Class II

• Medical Device Recall · September 18, 2025

  Cardinal Health 200, LLC

  Salem Sump PVC Tubes: Product Code/Product Name: 8888264911E ENFit" SALEM SUMP" PVC TUBE 10FR 36IN 8888264929E ENFit" SALEM SUMP" PVC TUBE 12FR 48IN 8888264945E ENFit" SALEM SUMP" PVC TUBE 14F

  Firm has received complaints regarding Anti-Reflux Valve (ARV) breakage due to excessive force during use. Firm is providing additional guidance for use. Expansion of RES 95214.

  Class II

• Medical Device Recall · September 18, 2025

  Cardinal Health 200, LLC

  Salem Sump PVC Tubes: Product Code/Product Name: 266122 Salem Sump" Stomach Tube, Dual Lumen with Anti-Reflux Valve, 14 Fr/Ch (4.7 mm) 266130 Salem Sump" Stomach Tube, Dual Lumen with Anti-Reflux

  Firm has received complaints regarding Anti-Reflux Valve (ARV) breakage due to excessive force during use. Firm is providing additional guidance for use. Expansion of RES 95214.

  Class II