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. 2,349 recalls have been distributed to South Dakota in the last 12 months.
Showing 27341–27360 of 27,558 recalls
Recalled Item: Sigma Spectrum VOLUMETRIC INFUSION PUMP Recalled by Baxter Healthcare...
The Issue: Recall expansion; the infusion pumps have the potential to fail causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genesis Straight Esthetic 5.0 mm 3. mm Cuff Abutment Part Recalled by...
The Issue: Mislabeled: Genesis Straight Esthetic 4.0mm Contour ,1mm cuff labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genesis Straight Esthetic 4.0 mm 1mm Cuff Abutment Part Number: Recalled by...
The Issue: Mislabeled: Genesis Straight Esthetic 5.0mm Contour ,3mm cuff labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catheter Irrigation Set labeled in part: ***24K Arthroscopy Outflow/Suction...
The Issue: ConMed Linvatec recalled their 24k Arthroscopy Outflow/Suction Tubing Set...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: epoc Blood Analysis BGEM Test Cards for use with the Recalled by Epocal Inc...
The Issue: Customer reported problem while performing incoming QC of newly received lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ******eMax 2 Plus Console***SN G 10307653002*** Product Usage: The Recalled...
The Issue: The RPM of the Motor Handpiece may be less than 80,000 RPM.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ******eMax 2 Plus Console Recalled by The Anspach Effort, Inc. Due to The...
The Issue: The RPM of the Motor Handpiece may be less than 80,000 RPM.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ******eMax 2 Plus Console Recalled by The Anspach Effort, Inc. Due to The...
The Issue: The RPM of the Motor Handpiece may be less than 80,000 RPM.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Z-800 Volumetric Infusion System. For intravenous infusion of parenteral...
The Issue: Update Instruction For Use for Preventative Maintenance (PM) Schedule and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioDerm Safe n' Dry 21006 (Component: SKIN-PREP Protective wipes). The...
The Issue: On 06/08/2011, BioDerm, Inc. issued a voluntary recall of a component (Smith...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioDerm Liberty Pouch Clean & Dry External Male Catheter Specialty Recalled...
The Issue: On 06/08/2011, BioDerm, Inc. issued a voluntary recall of a component skin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioDerm Liberty 3.0 External Male Catheter Specialty Type with integral...
The Issue: On 06/08/2011, BioDerm, Inc. issued a voluntary recall of a component skin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Varian High Energy Clinacs Recalled by Varian Medical Systems, Inc. Oncology...
The Issue: Under certain conditions, photon beams in High Energy Clinacs may experience...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neptune¿ 2 Rover - ULTRA ~120V ~ 60 Hz 12A Recalled by Stryker Instruments...
The Issue: Beginning May 24, 2011 Stryker Neptune 2 (N2) Waste Management Systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neptune¿ 2 Rover - ULTRA ~230V ~ 50 Hz 12A Recalled by Stryker Instruments...
The Issue: Beginning May 24, 2011 Stryker Neptune 2 (N2) Waste Management Systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ******Qty 1*** EC REP*** ConMed Linvatec Xenon Light Source Recalled by...
The Issue: Linvatec Corporation dba ConMed Linvatec, Largo, FL initiated a recall of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ******Qty 1*** EC REP*** ConMed Linvatec Xenon Universal Light Source...
The Issue: Linvatec Corporation dba ConMed Linvatec, Largo, FL initiated a recall of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DPM Central Station Mindray DS USA Recalled by Mindray DS USA, Inc. d.b.a....
The Issue: There is a software anomaly with the DPM Central Monitoring System where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cutting Bur Chart (part number 20-0019) utilized with the Electric Recalled...
The Issue: Anspach Effort, Inc. Palm Beach Gardens, FL initiated a correction of its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pneumatic Systems Operating Manual (part numbers 19-0005) utilized with the...
The Issue: Anspach Effort, Inc. Palm Beach Gardens, FL initiated a correction of its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.