- Home
- South Dakota Recalls
South Dakota Recalls
1,979 recalls on record affecting South Dakota
Pepsico Inc recalls 28 oz. Gatorade Lemon Lime, Gatorade Lemon Lime Zero, Gatora
Undeclared Yellow No. 6 and/or Yellow No. 5
View recall details →
G L Mezzetta Inc recalls Mezzetta GOLDEN GREEK PEPERONCINI MEDIUM HEAT 32 FL OZ G.L.
Potential contamination with foreign objects: mice.
View recall details →
Bard Access Systems, Inc. recalls DuoGlide Short-Term Straight Dialysis Catheter, REF: 5625150
this is a downstream recall of class I recall RES 98777
View recall details →
BD SWITZERLAND SARL recalls BD Alaris Pump Infusion Sets 10561554* 10885403232565 508854
Due to discrepancies in specific attributes in the performance data for infusion sets, which may lead to inappropriate pump performance.
View recall details →
Bard Access Systems, Inc. recalls Power-Trialysis Short-Term Straight Dialysis Catheter, REF:
this is a downstream recall of class I recall RES 98777
View recall details →
SDI Limited recalls Dentsply Sirona Capsule Mixer Model No. 5546068
Potential for electrical discharge from unit when unplugged.
View recall details →
Byron White Formulas, Inc. recalls Byron White FORMULAS A-L Complex Herbal Supplement 1.0 fl. o
Label does not declare walnuts in English
View recall details →
Byron White Formulas, Inc. recalls Byron White FORMULAS A-P Herbal Supplement 1.0 fl. oz./30 mL
Label does not declare walnuts in English
View recall details →
Byron White Formulas, Inc. recalls Byron White FORMULAS A-FNG Herbal Supplement 1.0 fl. oz./30
Label does not declare walnuts in English
View recall details →
BD SWITZERLAND SARL recalls 60 In Non-DEHP Minibore Extension Set RES ME2010 UDI-DI cod
Products may not have received adequate sterilization processing.
View recall details →
Kerry, Inc recalls KC Everyday Mac & Cheese, 3lb x 6. Item # 20609055. 6 - 3
Undeclared allergen (egg)
View recall details →
Orthofix U.S. LLC recalls Orthofix MINIRAIL, SHORT, LENGTHENER REF: M103, Unilateral
Unilateral external fixation devices may be incorrectly labeled. Minirail M101 was labeled as M103, Minirail M103 was labeled as M101, and Minirail M122 was labeled as M111
View recall details →
Orthofix U.S. LLC recalls Orthofix MINIRAIL, ARTICULATED, FIXATOR, VERTICAL AXIS REF:
Unilateral external fixation devices may be incorrectly labeled. Minirail M101 was labeled as M103, Minirail M103 was labeled as M101, and Minirail M122 was labeled as M111
View recall details →
Orthofix U.S. LLC recalls Orthofix ARTICULATED MINIRAIL FIXATOR HORIZONTAL AXIS REF:
Unilateral external fixation devices may be incorrectly labeled. Minirail M101 was labeled as M103, Minirail M103 was labeled as M101, and Minirail M122 was labeled as M111
View recall details →
Orthofix U.S. LLC recalls Orthofix MINIRAIL, STANDARD LENGTHENER Model/Catalog Number
Unilateral external fixation devices may be incorrectly labeled. Minirail M101 was labeled as M103, Minirail M103 was labeled as M101, and Minirail M122 was labeled as M111
View recall details →
AMY'S KITCHEN INC. recalls Amy's ORGANIC SOUPS LENTIL LIGHT IN SODIUM NET WT. 14.5 OZ
Potential for spoilage.
View recall details →
Nutricia North America recalls functional formularies NOURISH ORGANIC WHOLE FOODS MEAL REPL
Subpotent for Vitamin A. The firm discovered that the testing laboratory used the wrong method when testing for Vitamin A. The test results gave a higher concentration of vitamin A than what is actually in the product.
View recall details →
Nutricia North America recalls functional formularies LIQUID HOPE ORGANIC WHOLE FOODS MEAL
Subpotent for Vitamin A. The firm discovered that the testing laboratory used the wrong method when testing for Vitamin A. The test results gave a higher concentration of vitamin A than what is actually in the product.
View recall details →
Encore Medical, LP recalls Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS,
Due to packaging discrepancy with incorrect product size mixed up.
View recall details →
Encore Medical, LP recalls Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS,
Due to packaging discrepancy with incorrect product size mixed up.
View recall details →
Showing 20 of 1,979 recalls. Use search to filter further.