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Consumer Product Recalls
127,502 recalls from the U.S. Consumer Product Safety Commission, newest first.
January 8, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline custom medical procedure kits labeled as: 1) PANENDOSCOPY-LF, REF DYNJ36728C; 2) ENDOSCOPIC SINUS PACK, REF
Hazard: Custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical Strips, which have the potential for endotoxin contamination.
January 8, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline custom medical procedure kits labeled as: 1) ENDOSCOPIC SKULL BASE, REF DYNJ58648B; 2) ENDOSCOPIC SKULL BAS
Hazard: Custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical Strips, which have the potential for endotoxin contamination.
January 8, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline custom medical procedure kits labeled as: 1) FREE FLAP BASIC SET-UP PK, REF DYNJ0991320J; 2) MVFF/FIBU #54-
Hazard: Custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical Strips, which have the potential for endotoxin contamination.
January 8, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls See DocMan
Hazard: Custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical Strips, which have the potential for endotoxin contamination.
January 8, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline custom medical procedure kits labeled as: 1) NASAL PACK, REF DYNJ67789A.
Hazard: Custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical Strips, which have the potential for endotoxin contamination.
January 8, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline custom medical procedure kits labeled as: 1) UMC DR. BAKER SUPPLEMENT, REF DYNJ69476; 2) DIEP FLAP, REF DYN
Hazard: Custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical Strips, which have the potential for endotoxin contamination.
January 8, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline custom medical procedure kits labeled as: 1) VP SHUNT CDS, REF CDS983470D; 2) 1/2X1/2 NEURO SPONGE PACK-LF,
Hazard: Custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical Strips, which have the potential for endotoxin contamination.
January 8, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline custom medical procedure kits labeled as: 1) OPEN HEART CDS-LF, REFCDS840451M; 2) NEURO PACK, REFDYNJ41516M
Hazard: Custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical Strips, which have the potential for endotoxin contamination.
January 8, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline custom medical procedure kits labeled as: 1) CATH LAB PACK-LF, REF DYNJ0382559M; 2) CRANI, REF DYNJ56001B;
Hazard: Custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical Strips, which have the potential for endotoxin contamination.
January 8, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 8), Product Code 35700BAX2
Hazard: Devices were identified as released after repair without full testing being performed, which includes flow testing.
January 8, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6), Product Code 35700BAX
Hazard: Devices were identified as released after repair without full testing being performed, which includes flow testing.
January 8, 2025Medical DevicesFDA
Medtronic Neuromodulation recalls SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900E CLINICIAN TABLET GLBL SMS
Hazard: Software issues were identified in application version 2.x.
January 8, 2025Medical DevicesFDA
Medtronic Neuromodulation recalls SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900D CLINICIAN TABLET GLOBAL w
Hazard: Software issues were identified in application version 2.x.
January 8, 2025Medical DevicesFDA
Medtronic Neuromodulation recalls SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900C CLINICIAN TABLET UK with
Hazard: Software issues were identified in application version 2.x.
January 8, 2025Medical DevicesFDA
Medtronic Neuromodulation recalls SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900B CLINICIAN TABLET EU -UK w
Hazard: Software issues were identified in application version 2.x.
January 8, 2025Medical DevicesFDA
Angiodynamics, Inc. recalls AURYON LASER SYSTEM 100-120 VAC. Model Number: EXM001. Product Number: EXM-2001-1100
Hazard: Potential for procedural delays or interruptions during use of the Auryon Atherectomy System due to the Auryon Atherectomy System not advancing to the Activation (Ready) mode.
January 8, 2025Food & BeverageFDA
Heber Valley Artisan Cheese, LLC. recalls Cascade Raw Cheddar GTIN #90854115003059 packed in an approximately 6 lb quarter wheels vacuum sealed. All quarter whe
Hazard: The Cascade Raw Cheddar Cheese was recalled due to Shiga toxin-producing E. coli (STEC) and elevated generic E.coli in finished product testing results.
January 8, 2025Food & BeverageFDA
GARDNER'S CANDIES , INC recalls Gardner's Candies Cappuccino Meltaway Bar 1.25 oz. (35g), Item Number: 15207/online website item number is 0015207, sold
Hazard: Product contains Undeclared Allergen Tree Nuts (Cashews)
January 8, 2025Food & BeverageFDA
Herr Foods Inc recalls Wegmans Jalapeno Baked Cheese Puffs, Jalapeno flavored, 10oz, (283 g), SKU #6877
Hazard: Undeclared monosodium glutamate, sodium diacetate, disodium inosinate and disodium guanylate, and spice extract
January 8, 2025Food & BeverageFDA
BALOIAN FARMS recalls whole fresh American cucumbers packaged in bulk cardboard containers labeled with the "Pamela" brand, a generic white bo
Hazard: Cucumbers potentially contaminated with Salmonella.
January 8, 2025Food & BeverageFDA
Delta Fresh LLC. recalls Product is a whole, fresh cucumber with no individual packaging, labeling, PLU, or other identifying information. Cucumb
Hazard: Potential Salmonella contamination of fresh cucumbers. Associated with an outbreak.
January 8, 2025Food & BeverageFDA
RUSS DAVIS WHOLESALE recalls Kowalski's Garden Salad Net Wt. 14oz. Keep Refrigerated. UPC 7 95631-89335 9. Containing Lettuce, Cucumber, Tomato
Hazard: Cucumbers have potential to be contaminated with Salmonella.
January 8, 2025Food & BeverageFDA
RUSS DAVIS WHOLESALE recalls Crazy Fresh Turkey Havarti Wrap, Net Wt 6.8oz. Keep Refrigerated. UPC 7 95631-81149 0. Containing Flour Tortilla,
Hazard: Cucumbers have potential to be contaminated with Salmonella.
January 8, 2025Food & BeverageFDA
RUSS DAVIS WHOLESALE recalls Bacon Avocado Wrap, Net Wt 9.9oz. Keep Refrigerated. UPC 7 95631-81038 7. Containing Flour Tortilla,Carrots, Lettu
Hazard: Cucumbers have potential to be contaminated with Salmonella.
January 8, 2025Food & BeverageFDA
RUSS DAVIS WHOLESALE recalls Garden Salad w/Ranch Dressing, Net Wt 9oz. Keep Refrigerated. UPC 7 95831-81023 3. Containing Lettuce, tomatoes, c
Hazard: Cucumbers have potential to be contaminated with Salmonella.
January 8, 2025Food & BeverageFDA
RUSS DAVIS WHOLESALE recalls Whole and Cut Cucumbers packaged in the following sizes: 1. Peak Cucumber Item 08027, 24 count. Product of Mexico.
Hazard: Cucumbers have potential to be contaminated with Salmonella.
January 8, 2025Food & BeverageFDA
Minnesota Milk Bank for Babies recalls MN Milk Bank for Babies Pasteurize Donor Human Milk. Volume: 4 fl. oz. / 120 ml. Milk Type: 20 kcal/oz. 1.0 g/dL To
Hazard: Foreign material. (undetermined)
January 8, 2025Food & BeverageFDA
Sam'S Club recalls Member's Mark Hatch Chile Chicken Enchiladas, ready to cook, perishable, packaging type: aluminum/black oven-safe tray N
Hazard: Presence of Listeria monocytogenes
January 8, 2025Food & BeverageFDA
Reser's Fine Foods, Inc. recalls FCF Item 404885, Gyro Kit No Trays. Each box consists of 2/5.25lbs. packages. UPC 0 13454 38158. Distributed by Fresh Cr
Hazard: Salmonella. Item 404885, Gyro Kit No Trays contains implicated cucumber in the tzatziki sauce cup.
January 8, 2025Food & BeverageFDA
Reser's Fine Foods, Inc. recalls FCF Item 404884, Gyro Kit With Trays. Each tray consists of 2/5.25lbs. packages. UPC 0 13454 38155. Distributed by Fresh
Hazard: Salmonella. Item 404884, Gyro Kit With Trays contains implicated cucumber in the tzatziki sauce 2oz. cup.