RecallWatchUSA

Home / Recalls

Consumer Product Recalls

127,244 recalls from the U.S. Consumer Product Safety Commission, newest first.

December 17, 2025Medical DevicesFDA
Medline Industries, LP recalls Quick Strip Plastic Sterile Adhesive Bandages, 1" x 3", Medline Item Number NON25600QS
Hazard: Medline has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may exhibit open seals in the packaging which may compromise the sterility of the product.
December 17, 2025Medical DevicesFDA
Medline Industries, LP recalls Quick Strip Plastic Sterile Adhesive Bandages, 0.75" x 3", Medline Item Number NON25500QS
Hazard: Medline has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may exhibit open seals in the packaging which may compromise the sterility of the product.
December 17, 2025Medical DevicesFDA
Medline Industries, LP recalls Curad Quick Strip Fabric Bandages Containing 30 Bandages of 3/4" x 3", Medline Item Number CUR1930P
Hazard: Medline has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may exhibit open seals in the packaging which may compromise the sterility of the product.
December 17, 2025Medical DevicesFDA
Medline Industries, LP recalls CURAD Germ-Shield Touch-Free Fabric Bandages, Sterile, 0.75" x 3", 30/Box, Medline Item Number CUR1930F
Hazard: Medline has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may exhibit open seals in the packaging which may compromise the sterility of the product.
December 17, 2025Medical DevicesFDA
Cardinal Health 200, LLC recalls ChemoPlus gowns: Product Code Product Description CT5500T ChemoPlus Full Coverage Sleeve, Universal, Medium Blue, Non-
Hazard: Affected gowns have the incorrect expiration date on the product packaging. Product has a shelf-life of three years which is mislabeled on the product packaging as five (5) years.
December 17, 2025Medical DevicesFDA
Orthofix U.S. LLC recalls Brand Name: CONSTRUX" Mini Ti Spacer System Product Name: CONSTRUX" Mini Ti Spacer System Model/Catalog Number: 37-600
Hazard: Labeling contains claims that are not consistently present.
December 17, 2025Medical DevicesFDA
Orthofix U.S. LLC recalls Brand Name: Forza" Ti Spacer System Product Name: Forza" Ti Spacer System Model/Catalog Number: 38-2006SP FORZA Ti Spa
Hazard: Labeling contains claims that are not consistently present.
December 17, 2025Medical DevicesFDA
Orthofix U.S. LLC recalls Brand Name: FIREBIRD" SI Fusion System Product Name: FIREBIRD" SI Fusion System Model/Catalog Number: 18-1025SP 11mm X
Hazard: Labeling contains claims that are not consistently present.
December 17, 2025Medical DevicesFDA
Orthofix U.S. LLC recalls Brand Name: Pillar" SA PTC Spacer System Product Name: Pillar" SA PTC Spacer System Model/Catalog Number: 39-9012SP 33
Hazard: Labeling contains claims that are not consistently present.
December 17, 2025Medical DevicesFDA
Orthofix U.S. LLC recalls Brand Name: FORZA" PTC Spacer System Product Name: FORZA" PTC Spacer System Model/Catalog Number: 38-1007SP FORZA PTC
Hazard: Labeling contains claims that are not consistently present.
December 17, 2025Medical DevicesFDA
Orthofix U.S. LLC recalls Brand Name: CONSTRUX" Mini PTC Spacer System Product Name: CONSTRUX" Mini PTC Spacer System Model/Catalog Number: 37-3
Hazard: Labeling contains claims that are not consistently present.
December 17, 2025Medical DevicesFDA
Waldemar Link GmbH & Co. KG (Mfg Site) recalls Endo Model Knee Fusion Nail SK, Knee Fusion Nail, Coupling Component, right, modular, L= 68 mm, Taper 10/12. Knee compo
Hazard: The device has been delivered with a preassembled locking screw that had been inserted from the wrong side into the male taper of the femoral component.
December 17, 2025Medical DevicesFDA
Beckman Coulter, Inc. recalls Access 2 Reaction Vessels, individual, disposable, plastic tubes used to process patient, quality control and calibratio
Hazard: It has been determined that certain lots of Access 2 Reaction Vessels may contain manufacturing deformities. The bottom (round end) of the Reaction Vessel may have a small protrusion or hair like deformity. This could cause causing instrument errors (e.g., pipetting, rake, wash carousel errors) that could delay patient results.
December 17, 2025Medical DevicesFDA
Bard Peripheral Vascular Inc recalls Safe-T-Centesis 6 Fr Catheter Drainage Tray, REF: PIG1260T,
Hazard: Acute drainage catheters, indicated for use in removing fluid during acute drainage/aspiration procedure, manufactured with safety indicators that erroneously show catheter in sharp position when catheter is in blunt position, which may lead users to believe device is not yet in pleural or peritoneal space when it is, may cause discomfort, delay to treatment, injury to internal organs or vessels.
December 17, 2025Medical DevicesFDA
Medline Industries, LP recalls MEDLINE PERFUSION SYRINGE, REF: DYNJ39223C
Hazard: Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing BD Luer Tip Caps. BD has issued a recall of their Luer Tip Caps after confirming through internal testing that certain BD Luer Tip Cap trays failed routine biocompatibility testing. Although the tip cap covers a small surface area of the syringe and does not come in direct contact with patients, there is the potential that the failure of a biocompatibility test may have varying consequences ranging from no harm or clinical impact to potential for sensitization, irritation, pyrogenicity, acute systemic toxicity or hemolysis depending on the nature and duration of contact with the syringe.
December 17, 2025Medical DevicesFDA
GE Medical Systems, LLC recalls Senographe Pristina, Pristina Serena, and Pristina Serena 3D. for screening and diagnostic mammography
Hazard: Some Senographe Pristina systems either have a missing or an incorrect X-Ray Warning label, which is a nonconformance to FDA Regulation 21 CFR ¿1020.30(j).
December 17, 2025Medical DevicesFDA
Philips North America recalls Azurion R3.0. Model Number 722234. Commercial Name: Azurion 7 M20. INTERVENTIONAL FLUOROSCOPIC XRAY SYSTEM
Hazard: Between July 2024 and June 2025, Philips Azurion R3.0 systems with a FlexArm stand were shipped without the Source-to-Skin Distance (SSD) Spacer. The SSD spacer is necessary to meet the FDA minimum source-skin distance requirement of 38 cm for standard fluoroscopy applications.
December 17, 2025Medical DevicesFDA
Draeger, Inc. recalls ErgoStar CM 60, Model/Catalog Number: MP01860, Airway connector for conduction of respiratory gases between the
Hazard: Multiple complaints were reported in which cracks formed in the hose of specific catheter mounts.
December 17, 2025Medical DevicesFDA
Draeger, Inc. recalls ErgoStar CM 55, Model/Catalog Number: MP01855, Airway connector for conduction of respiratory gases between the
Hazard: Multiple complaints were reported in which cracks formed in the hose of specific catheter mounts.
December 17, 2025Medical DevicesFDA
Draeger, Inc. recalls ErgoStar CM 45, Model/Catalog Number: MP01845, Airway connector for conduction of respiratory gases between the b
Hazard: Multiple complaints were reported in which cracks formed in the hose of specific catheter mounts.
December 17, 2025Medical DevicesFDA
Draeger, Inc. recalls ErgoStar CM 40 Model/Catalog Number: MP01840 Airway connector for conduction of respiratory gases between the brea
Hazard: Multiple complaints were reported in which cracks formed in the hose of specific catheter mounts.
December 17, 2025Food & BeverageFDA
Moonlight Packing Corporation recalls Sticker label (for Loose Bulk - peppermint peaches): 4401
Hazard: Potential contamination with Listeria monocytogenes.
December 17, 2025Food & BeverageFDA
Moonlight Packing Corporation recalls Sticker label (for Loose Bulk - peppermint peaches): 4401
Hazard: Potential contamination with Listeria monocytogenes.
December 17, 2025Food & BeverageFDA
Moonlight Packing Corporation recalls Sticker label (for Loose Bulk - white peaches): 4401
Hazard: Potential contamination with Listeria monocytogenes.
December 17, 2025Food & BeverageFDA
Moonlight Packing Corporation recalls Sticker label (for Loose Bulk - yellow peaches): 4044
Hazard: Potential contamination with Listeria monocytogenes.
December 17, 2025Food & BeverageFDA
Moonlight Packing Corporation recalls Sticker label (for Loose Bulk - yellow peaches): 4044
Hazard: Potential contamination with Listeria monocytogenes.
December 17, 2025Food & BeverageFDA
Moonlight Packing Corporation recalls UPC 8 98429 00266 4 Peppermint Peach PROUCE OF U.S.A. 4 COUNT MIN. WT. 2.25 LBS MOONLIGHT PACKING CORPORATION REEDLEY, C
Hazard: Potential contamination with Listeria monocytogenes.
December 17, 2025Food & BeverageFDA
Moonlight Packing Corporation recalls UPC 8 10248 03186 1 Peppermint Peach PRODUCE OF U.S.A. NET WT. 2 LBS. (907G) MOONLIGHT PACKING CORPORATION REEDLEY, CA 9
Hazard: Potential contamination with Listeria monocytogenes.
December 17, 2025Food & BeverageFDA
Moonlight Packing Corporation recalls UPC 8 10248 03186 1 WHITE PEACHES CALIFORNIA FRUIT PRODUCE OF U.S.A. NET WT. 2 LBS. (907G) MOONLIGHT PACKING CORP. REEDL
Hazard: Potential contamination with Listeria monocytogenes.
December 17, 2025Food & BeverageFDA
Moonlight Packing Corporation recalls UPC 8 98429 00209 1 PEACHES PRODUCE OF U.S.A. NET WT 2 LB (32 OZ) 907 g DISTRIBUTED BY MOONLIGHT PACKING CORP. REEDLEY,
Hazard: Potential contamination with Listeria monocytogenes.