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. 1,030 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
1,030 in last 12 months

Showing 15281–15300 of 47,632 recalls

Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: Left Heart Kit Recalled by Smiths Medical ASD Inc. Due to Specific lots of...

The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: Stopcock rotator (Component): a. 1050 STOPCOCK ROTATOR Recalled by Smiths...

The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: LogiCal Left Heart Kit Recalled by Smiths Medical ASD Inc. Due to Specific...

The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Welch Allyn Inc Mortara

Recalled Item: AM12M Acquisition Module accessory. Impacted software version of the AM12M...

The Issue: Devices do not meet IEC 60601-2-27 requirements as labeled.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: Manifold rotator (Component): a. 250 2 GANG MANIFOLD ROTATOR Recalled by...

The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: HIGH PRESSURE TUBING Recalled by Smiths Medical ASD Inc. Due to Specific...

The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: Medex 10 IN Pressure Injector Line w/Rot (1200psi) NS. Recalled by Smiths...

The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: HIGH PRESSURE ROTATOR (Component) a. WITH MALE LUER LOCK Recalled by Smiths...

The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: Artis systems - Product Usage: an angiography systems developed for Recalled...

The Issue: Due to inappropriate cleaning, some Artis systems show unexpected corrosion...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugMarch 30, 2021· Na Na Collection

Recalled Item: Triple SupremeZen Gold 3500 Recalled by Na Na Collection Due to Marketed...

The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 30, 2021· Ummzy, LLC

Recalled Item: Krazy Night capsule Recalled by Ummzy, LLC Due to Undeclared Tadalafil

The Issue: Marketed Without An Approved NDA/ANDA: Products found to contain undeclared...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugMarch 30, 2021· Ummzy, LLC

Recalled Item: Shogun-X capsules Recalled by Ummzy, LLC Due to Undeclared Tadalafil

The Issue: Marketed Without An Approved NDA/ANDA: Products found to contain undeclared...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugMarch 30, 2021· Na Na Collection

Recalled Item: PremierZen Platinum 5000 Recalled by Na Na Collection Due to Marketed...

The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 30, 2021· Ummzy, LLC

Recalled Item: Thumbs up 7 Red 70K capsules Recalled by Ummzy, LLC Due to Undeclared Tadalafil

The Issue: Marketed Without An Approved NDA/ANDA: Products found to contain undeclared...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugMarch 29, 2021· Spartan Chemical Co Inc

Recalled Item: Lite'n Foamy Eucalyptus Mint Sanitizing Handwash (Benzalkonium Chloride...

The Issue: CGMP Deviations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 29, 2021· Spartan Chemical Co Inc

Recalled Item: Lite'n Foamy Lemon Blossom Hand Sanitizer (benzalkonium chloride 0.1%)...

The Issue: Microbial Contamination of Non-Sterile Products; lot tested positive for...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugMarch 29, 2021· Spartan Chemical Co Inc

Recalled Item: Antiseptic Hand Cleaner (Chloroxylenol Recalled by Spartan Chemical Co Inc...

The Issue: CGMP Deviations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 29, 2021· Spartan Chemical Co Inc

Recalled Item: Lite'n Foamy Healthcare Personnel Handwash (Chloroxylenol Recalled by...

The Issue: CGMP Deviations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 29, 2021· Spartan Chemical Co Inc

Recalled Item: Lite'n Foamy E2 Sanitizing Handwash (Benzalkonium Chloride Recalled by...

The Issue: CGMP Deviations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 29, 2021· Spartan Chemical Co Inc

Recalled Item: foamyiQ Lemon Blossom Hand Sanitizer (benzalkonium chloride 0.1%) Recalled...

The Issue: CGMP Deviations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund