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. 2,429 recalls have been distributed to South Dakota in the last 12 months.
Showing 19321–19340 of 27,558 recalls
Recalled Item: CORE¿ Suction Irrigation Handpiece Y-Tubing set Recalled by ConMed...
The Issue: The packaging seal may contain a crease. The crease may result in an open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORE¿ Suction Irrigation Handpiece without Probe for Single Solution Bags...
The Issue: The packaging seal may contain a crease. The crease may result in an open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORE¿ Trumpet Handpiece only Recalled by ConMed Corporation Due to The...
The Issue: The packaging seal may contain a crease. The crease may result in an open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORE¿ Trumpet Handpiece with 5mm x 32cm Length Probe Recalled by ConMed...
The Issue: The packaging seal may contain a crease. The crease may result in an open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORE¿ Suction Irrigation Handpiece with 5mm x 32cm Length Probe Recalled by...
The Issue: The packaging seal may contain a crease. The crease may result in an open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORE¿ Suction Irrigation Handpiece with 5mm x 32cm Length Probe Recalled by...
The Issue: The packaging seal may contain a crease. The crease may result in an open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The 9025TRU Arterial Blood Gas (ABG) Kit is used to Recalled by Cardinal...
The Issue: Arterial Blood Gas (ABG) Kit- Missing Safety Component. The ABG Kit(s) have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adaptor for Small Battery Drive and Small Battery Drive II. Recalled by The...
The Issue: There was a potential for the Adaptor and Light Adaptor for Small Battery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Molift Air 205 Recalled by Moller Vital Due to Potential for the bolt on the...
The Issue: Potential for the bolt on the suspension coupling on the Molift Air to come...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.3MM Tapered Router Recalled by Stryker Instruments Div. of Stryker...
The Issue: A variation in flute depth on the routers was observed. The variation in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synovis VASCU-GUARD Peripheral Vascular Patch in the following sizes and...
The Issue: Baxter is issuing a safety alert in response to postmarketing reports...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Trucount Tubes: Catalog number: 340334 Hematology: BD Trucount tubes...
The Issue: One lot of BD Trucount Absolute Counting Tubes (IVD) may not be sealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roadrunner Uniglide Hydrophilic Wire Guide Recalled by Cook Inc. Due to...
The Issue: Potential coating contamination with glass particles.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Light Adaptor for Small Battery Drive and Small Battery Drive II. Recalled...
The Issue: There was a potential for the Adaptor and Light Adaptor for Small Battery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EtCO2 Module -Part Number: 02.01.210699 Monitors: iM80 Recalled by Edan...
The Issue: Incorrect CO2 readings with some patient monitors.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mindray DS USA Inc. Recalled by Mindray DS USA, Inc. dba Mindray North...
The Issue: Mindray has identified a potential leakage issue with the CO2 Module's...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthopaedics Modular Handle Triathlon Instruments Recalled by...
The Issue: Stryker Orthopaedic is voluntarily recalling the Triathlon Modular Handle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthopaedics Specialty Triathlon Tibial Alignment Handle with...
The Issue: It was reported that the secondary locking mechanism, and its corresponding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.via Recalled by Siemens Medical Solutions USA, Inc Due to Incorrect...
The Issue: Incorrect values for the volume calculation. Software update VB30B via...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optical Surface Monitoring System{Align RT Plus} This is used on Recalled by...
The Issue: Varian Medical Systems has received reports that unintended changes were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.