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. 2,311 recalls have been distributed to South Dakota in the last 12 months.
Showing 39781–39800 of 47,632 recalls
Recalled Item: Name: Pasteur Pipets Recalled by ORIGIO, Inc Due to Identification of...
The Issue: Identification of packaging breach of the nylon pouch sterile barrier for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diltiazem HCl Extended Release Capsules Recalled by Mylan Pharmaceuticals...
The Issue: Failed Impurities/Degradation Specifications: High out-of-specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Aspirin DR Enteric Coated Tablets Recalled by Mckesson Packaging Services...
The Issue: Failed Dissolution Specification; at the 12 month time interval.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cardura XL (doxazosin mesylate extended release tablets Recalled by Pfizer...
The Issue: Failed Impurities/Degradation Specifications: Product from this lot may not...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bystolic (nebivolol) tablets Recalled by Forest Pharmaceuticals Inc Due to...
The Issue: Failed Dissolution Specifications: Drug failed stage III dissolution testing.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Country Life TARGET MINS CALCIUM MAGNESIUM With Vitamin D3 Complex Recalled...
The Issue: The affected lots do not meet quality standards due to insoluble particulates.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 5 mL Reaction Vessels (a consumable of the Abbott m2000sp Recalled by Abbott...
The Issue: Abbott Molecular identified that some of the 5 ml Reaction Vessels (RVs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific ENDOTAK RELIANCE¿ SG Recalled by Boston Scientific CRM...
The Issue: A review of manufacturing test records for Boston Scientific ENDOTAK...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Marcaine (bupivacaine HCl) injection Recalled by Hospira Inc. Due to...
The Issue: Presence of Particulate Matter: Confirmed customer complaint of discolored...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Velivet (desogestrel and ethinyl estradiol tablets - triphasic regimen)...
The Issue: Failed Impurities/Degradation Specifications: out of specification impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Apri (desogestrel and ethinyl estradiol tablets USP) Recalled by Teva...
The Issue: Failed Impurities/Degradation Specifications: out of specification impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Kariva (desogestrel/ethinyl estradiol and ethinyl estradiol) Tablets 0.15...
The Issue: Failed Impurities/Degradation Specifications: out of specification impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mircette (desogestrel/ethinyl estradiol and ethinyl estradiol) Tablets 0.15...
The Issue: Failed Impurities/Degradation Specifications: out of specification impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: C-Series High Energy Linear Accelerator - Models: Novalis Tx Recalled by...
The Issue: Trend in reports of unexpected decrease in beam output in C-series High...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter MiniCap with Povidone-Iodine Solution Recalled by Baxter Healthcare...
The Issue: Inadequate iodine and packaging related defects.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo¿ Advanced Perfusion System 1 220/240V AC Recalled by Terumo...
The Issue: An evaluation of the APS1 Operator Manual found that existing instructions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo¿ Advanced Perfusion System 1 100/120V AC Recalled by Terumo...
The Issue: An evaluation of the APS1 Operator Manual found that existing instructions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brevibloc Premixed Injection Recalled by Baxter Healthcare Corp. Due to...
The Issue: Presence of Particulate Matter: Complaints received of discolored solution...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Non-Mydriatic Auto Fundus Camera. Model AFC-330. An ophthalmic camera for...
The Issue: Image taken by AFC-330 has a white spot which may affect diagnosis or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Paragon Laboratory Management Recalled by McKesson Technologies, Inc. Due to...
The Issue: For Paragon Laboratory Management 12.1 and 12.1.1 releases, if used with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.