South Dakota Recalls
1,956 recalls on record affecting South Dakota
Draeger, Inc. recalls Atlan A350. Model Number: 8211500. anesthesia workstation
The Atlan anesthesia workstation either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.
View recall details →
Intuitive Surgical, Inc. recalls Brand Name: Da Vinci 5 Product Name: ASSY,DV5 TOWER,IS5000
Due to unintentionally activated near infrared handheld camera when attempting to turn off illumination during normal clinical workflow transitions, particularly when switching from the handheld camera to the robotic endoscope.
View recall details →
Draeger, Inc. recalls Atlan A350XL. Model Number: 8621600. anesthesia workstation
The Atlan anesthesia workstation either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.
View recall details →
The Coffee Connexion Co., Inc recalls Cold Prep Cream Sauce, 20 lb., packaged in a tied poly bag a
Product contains dry milk powder ingredient recalled by the supplier due to potential Salmonella contamination
View recall details →
The Coffee Connexion Co., Inc recalls Alfredo Sauce, 3 lb. 7 oz., packaged in a sealed poly bag an
Product contains dry milk powder ingredient recalled by the supplier due to potential Salmonella contamination
View recall details →
The Coffee Connexion Co., Inc recalls 1) Cheese Sauce Mix, 25.5 oz., packaged in a sealed poly bag
Product contains dry milk powder ingredient recalled by the supplier due to potential Salmonella contamination
View recall details →
The Coffee Connexion Co., Inc recalls Aramark Cheese Sauce New & Improved, 25 lb., packaged in a t
Product contains dry milk powder ingredient recalled by the supplier due to potential Salmonella contamination
View recall details →
C.R. Bard Inc recalls Silastic Foley Catheters Silastic Brand Foley Catheter 30cc
Due to stain present on the surface of affected foley catheters.
View recall details →
French Broad Chocolate Factory recalls french broad CHOCOLATE bette's bake sale (a multi-flavor bon
Undeclared nut allergen (walnut) due to mislabeling. The product's printed tasting guide incorrectly identifies the Walnut Fudge and Peach Cobbler flavor chocolates (bonbons). Consumers relying on the printed materials could mistakenly consume a nut-containing bonbon.
View recall details →
Stryker Sustainability Solutions recalls Stryker Sustainability Solution Color Cuff 24" (Yellow) Quic
Due to potential for tourniquet cuffs to detach from the bladder at the welding connection and result in the cuff not being able to maintain pressure.
View recall details →
Savannah Bee Company Inc. recalls SAVANNAH BEE COMPANY HONEY BBQ SAUCE MUSTARD NET 16 FL OZ (4
Undeclared Allergens: Soy & Wheat. The firm was notified by a customer that the product is labeled as Savannah Bee Company Honey BBQ Sauce "Mustard", but the product inside the bottle is a different flavor of BBQ sauce. After investigation, the firm determined that the product in the bottle is their Honey BBQ Sauce "Sweet". The BBQ sauce "Sweet" contains wheat and soy which is not listed on the BBQ Sauce "Mustard" label.
View recall details →
GE Healthcare, LLC recalls Prestige II
GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2, Prestilix, Prestige VH, Prestige SI, RFX/SFX, Legacy, Precision 500D, ADVANTX and Innova 2000 systems.
View recall details →
Siemens Medical Solutions USA, Inc recalls SOMATOM Scope, Computed tomography x-ray system
Siemens is providing a new installation of the Residual Current Monitor (RCM) in the Line Connection Box (LCB) to resolve a potential defect that could lead to a power cutout during use of the SOMATOM Scope, Scope Power and Perspective systems.
View recall details →
Siemens Medical Solutions USA, Inc recalls SOMATOM Scope Power, Computed tomography x-ray system
Siemens is providing a new installation of the Residual Current Monitor (RCM) in the Line Connection Box (LCB) to resolve a potential defect that could lead to a power cutout during use of the SOMATOM Scope, Scope Power and Perspective systems.
View recall details →
Shimadzu Medical Systems recalls Shimadzu X-ray TV System, Catalog No. SONIALVISION G4
Shimadzu Medical Systems is recalling Shimadzu X-ray TV System SONIALVISION due to possibility of oil leaking from the x-ray tube housing under certain conditions.
View recall details →
GE Healthcare, LLC recalls SFX
GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2, Prestilix, Prestige VH, Prestige SI, RFX/SFX, Legacy, Precision 500D, ADVANTX and Innova 2000 systems.
View recall details →
GE Healthcare, LLC recalls ADVANTX LCN+
GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2, Prestilix, Prestige VH, Prestige SI, RFX/SFX, Legacy, Precision 500D, ADVANTX and Innova 2000 systems.
View recall details →
GE Healthcare, LLC recalls ADVANTX LCLP+
GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2, Prestilix, Prestige VH, Prestige SI, RFX/SFX, Legacy, Precision 500D, ADVANTX and Innova 2000 systems.
View recall details →
GE Healthcare, LLC recalls Legacy
GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2, Prestilix, Prestige VH, Prestige SI, RFX/SFX, Legacy, Precision 500D, ADVANTX and Innova 2000 systems.
View recall details →
GE Healthcare, LLC recalls Innova 2000
GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2, Prestilix, Prestige VH, Prestige SI, RFX/SFX, Legacy, Precision 500D, ADVANTX and Innova 2000 systems.
View recall details →
Showing 20 of 1,956 recalls. Use search to filter further.