Product Recalls in South Dakota
Product recalls affecting South Dakota — including food, drugs, consumer products, medical devices, and vehicles distributed to South Dakota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,516 recalls have been distributed to South Dakota in the last 12 months.
Showing 7481–7500 of 47,632 recalls
Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...
The Issue: Their is a potential for battery pins to become loose within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...
The Issue: Their is a potential for battery pins to become loose within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...
The Issue: Their is a potential for battery pins to become loose within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...
The Issue: Their is a potential for battery pins to become loose within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...
The Issue: Their is a potential for battery pins to become loose within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...
The Issue: Their is a potential for battery pins to become loose within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...
The Issue: Their is a potential for battery pins to become loose within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...
The Issue: Their is a potential for battery pins to become loose within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...
The Issue: Their is a potential for battery pins to become loose within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gynazole-1 Recalled by Padagis US LLC Due to Incorrect Product Formulation:...
The Issue: Incorrect Product Formulation: Hydrophilic Colloidal Silica was used to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Triamcinolone Acetonide Injectable Suspension Recalled by Eugia US LLC Due...
The Issue: Presence of Particulate Matter: A product complaint of a piece of glass was...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TRACHEAL INTUBATION FIBERSCOPE OLYMPUS LF-GP Recalled by Olympus Corporation...
The Issue: Fiberscopes do not have adequate data to support that the suction flow rate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edible Cookie Dough Chocolate Chip packaged in 6 oz plastic cups lot # 3240...
The Issue: Undeclared Peanut Butter; Packaged Peanut Butter Dough in Chocolate Chip...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: EXALT Model D Single-Use Duodenoscope: Outer box UPN# M00542420 & Recalled...
The Issue: Poor image quality due to fluid ingress in the lens.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXALT Model D Single-Use Duodenoscope Recalled by Boston Scientific...
The Issue: Poor image quality due to fluid ingress in the lens.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StealthStation S8 Application version 2.0 and 2.0.1 (Part 9735762) The...
The Issue: Due to a software anomaly which potentially could result in the surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JOURNEY II BCS CONSTRAINED ARTICULAR INSERT Size 5-6 Recalled by Smith &...
The Issue: The JRNY II BCS XLPE ART ISRT SZ 5-6 LT 10MM was laser etched, labeled and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JOURNEY II BCS ARTICULAR INSERT Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The JRNY II BCS XLPE ART ISRT SZ 5-6 LT 10MM was laser etched, labeled and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RAPIDPOINT 500 Blood Gas System Recalled by Siemens Healthcare Diagnostics...
The Issue: There are potential drug interferences from Perhexiline Maleate or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RAPIDPOINT 500e Blood Gas System Recalled by Siemens Healthcare Diagnostics...
The Issue: There are potential drug interferences from Perhexiline Maleate or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.