HIGH
FDA DEVICE
Medline Kits: 1) HEART TRANSPLANT BIOPSY, Model Number: DYNJ37543A
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Medline Industries, LP
The 510(k)
These recalls involve products that pose serious risks of injury or death. Check if you own any of these products and take immediate action if needed.
High Risk Recalls
3,609 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
What to do if you own a recalled product:
- Stop using the product immediately
- Keep the product away from children
- Follow the remedy instructions provided
- Contact the manufacturer for a refund or replacement
HIGH
FDA DEVICE
Medline Namic Guidewires: 1) GUIDEWIRE 3MMJ 0.035X260CM LT, Model Number: DYNJGWIRE20L; 2) GWIRE HYDRO 0.035 180CM ANG S, Model Number: DYNJHWIRE105; 3) GWIRE HYDRO 0.035 260CM ANG S, Model...
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Medline Industries, LP
The 510(k)
HIGH
FDA DEVICE
Medline Namic Syringes: 1) SYR CNTRL 10ML RING W/ROT NB, Model Number: DYNJSYR10CWRB;
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Medline Industries, LP
The 510(k)
HIGH
FDA DEVICE
Medline Kits: 1) BREAST PACK, Model Number: DYNJ66777D
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Medline Industries, LP
The 510(k)
HIGH
FDA DEVICE
Medline Kits: 1) LABOR PACK-22025208-LF, Model Number: DYNJ44813D
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Medline Industries, LP
The 510(k)
HIGH
FDA DEVICE
Medline Kits: 1) ARTHROSCOPY PACK, Model Number: DYNJ82440
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Medline Industries, LP
The 510(k)
HIGH
FDA DEVICE
Medline Syringes: 1) SYRINGE 12ML CONTROL W/ROTATOR, Model Number: DYNJSYR12CWR; 2) SYRINGE 10ML CONTROL W/ROTATOR, Model Number: DYNJSYR10CWR; 3) SYR CONTROL PAD 12ML L/L, Model Number:...
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Medline Industries, LP
The 510(k)
HIGH
FDA DEVICE
Medline Kits: 1) PICC TRAY, Model Number: DYNJ41648A
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Medline Industries, LP
The 510(k)
HIGH
FDA DEVICE
Medline Kits: 1) CATH LAB CDS, Model Number: CDS840228F; 2) IR PACK, Model Number: DYNDH2104; 3) CARDIAC CATH PACK-LF, Model Number: DYNJT2164M; 4) ANGIOGRAPHY TRAY, Model Number: DYNJT3078; 5)...
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Medline Industries, LP
The 510(k)
HIGH
FDA DEVICE
Medline Kits: 1) MTS LEFT HEART KIT-CAROLINAS HOS, Model Number: 60021775; 2) DBD-MTS LHK BHS BAPTIST. LOUISVI, Model Number: 60022026; 3) MTO LEFT HEART KIT SUMMA BARBERT, Model Number:...
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Medline Industries, LP
The 510(k)
HIGH
FDA DEVICE
Medline Kits: 1) BWNBORO CRANIOTOMY PACK-LF, Model Number: DYNJ32841F; 2) CRANIOTOMY PACK-LF, Model Number: DYNJ46069D 3) CAMPUS EXTREMITY PK, Model Number: DYNJ51935A 4) FOOT -XRAY BOWL MEDCUP...
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Medline Industries, LP
The 510(k)
Food & Beverages
HIGH
FDA FOOD
Novamex Coconut Water Recall Targets 12,000 Cases Over Packaging Nutrition Facts Discrepancy
A Tipp Distributors, Inc. dba Novamex recall affects 12,000 cases of C2O Coconut Water with Pulp sold across multiple states. The outer cardboard box lists an incorrect Nutrition Facts Panel and Ingredient List, omitting added sugar. The can itself has the correct information. Consumers should avoid consumption and seek refund or replacement.
Novamex
The outer
Pet Products
HIGH
FDA FOOD
Imu-Tek Animal Health Colostrum-5 Powder Recall 64 Bottles Across 29 States (2026)
Imu-Tek Animal Health recalled 64 bottles of Colostrum-5 Powder sold through multiple retailers. The recall covers products distributed in 29 states. The product is potentially under-processed. Consumers should stop using it and contact Imu-Tek Animal Health for refund or replacement.
Imu-Tek Animal Health
Product is
Food & Beverages
HIGH
FDA FOOD
King Harvest Balsamic Hummus Recalled for Aluminum Shards in 326 10oz Tubs (2026)
King Harvest Balsamic Hummus recalled by Pacific Coast Fresh Co. The product was distributed in Oregon and Washington. A foreign material aluminum piece hazard was identified. Consumers should not eat the product and should contact Pacific Coast Fresh Co for refund or replacement information by telephone.
Pacific Coast Fresh CO
Foreign material
Food & Beverages
HIGH
FDA FOOD
King Harvest Roasted Red Pepper Hummus Recalled for Aluminum Pieces in 683 Containers (2026)
King Harvest Roasted Red Pepper Hummus, distributed in Oregon and Washington by Pacific Coast Fresh Co, is recalled. The recall cites foreign material aluminum pieces found in 10 oz and 17 oz tubs. Consumers should not eat the product and should contact Pacific Coast Fresh Co for a refund or replacement.
Pacific Coast Fresh CO
Foreign material
Food & Beverages
HIGH
FDA FOOD
Pacific Coast Fresh CO Recalls King Harvest Sundried Tomato Hummus Over Aluminum Pieces (2026)
Pacific Coast Fresh CO recalls 348 10-ounce King Harvest Sundried Tomato Hummus containers sold in Oregon and Washington after aluminum pieces were found. The hazard is foreign material aluminum pieces in the hummus. Consumers should not consume the product and should contact Pacific Coast Fresh CO by telephone for refund or replacement.
Pacific Coast Fresh CO
Foreign material
Food & Beverages
HIGH
FDA FOOD
Pacific Coast Fresh CO Recalls King Harvest Spinach Hummus 2026 for Aluminum Fragments
Pacific Coast Fresh CO is recalling 239 containers of King Harvest Spinach Hummus sold in Oregon and Washington. Each 10-ounce tub bears UPC 025726311087 and Best By date 2/27/2026. Stop using the product immediately due to aluminum fragments and call Pacific Coast Fresh CO by telephone for refund or replacement.
Pacific Coast Fresh CO
Foreign material
Food & Beverages
HIGH
FDA FOOD
Pacific Coast Fresh Co. Recalls King Harvest Jalapeno Hummus for Aluminum Pieces (2026) — 760 Units
Pacific Coast Fresh Co. recalled 760 King Harvest Jalapeno Hummus containers distributed in Oregon and Washington. Aluminum pieces were found as a foreign material in the product. Consumers should not consume this hummus and should contact the company for refund or replacement.
Pacific Coast Fresh CO
Foreign material
Food & Beverages
HIGH
FDA FOOD
King Harvest Black Olive Hummus Recalled for Aluminum Pieces in 319 Containers (2026)
King Harvest Black Olive Hummus, sold in 10-ounce plastic tubs and distributed in Oregon and Washington, is recalled after aluminum fragments were found. The recall cites a foreign material hazard. Consumers who purchased it should not consume it and should contact Pacific Coast Fresh CO by telephone for a refund or replacement.
Pacific Coast Fresh CO
Foreign material
Pet Products
HIGH
FDA FOOD
Imu-Tek Animal Health Colostrum-5 Recall 2026: 1,003 Bottles Distributed Across 30 States
Imu-Tek Animal Health recalled 1,003 bottles of Colostrum-5 sold through various retailers in 30 states after determining the product may be under-processed. The under-processing could render the product unsafe. Consumers should not consume the product and should contact Imu-Tek Animal Health for refund or replacement.
Imu-Tek Animal Health
Product is
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