Product Recalls in Iowa
Product recalls affecting Iowa — including food, drugs, consumer products, medical devices, and vehicles distributed to Iowa. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,846 recalls have been distributed to Iowa in the last 12 months.
Showing 28441–28460 of 49,990 recalls
Recalled Item: Maquet Cardiopulmonary Bypass Custom Tubing kit BEQ-T 4906 PEDIARIC CPB PACK...
The Issue: There is a potential for the over-pressure safety (OPS) valve in the tubing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Cardiopulmonary Bypass Custom Tubing kit BO-TOP 38600 ADULT CPB...
The Issue: There is a potential for the over-pressure safety (OPS) valve in the tubing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.T.S. 2200TS Tourniquet Systems Recalled by Zimmer Surgical Inc Due to...
The Issue: Updated on-device label and 3 pages of an updated Operator/Service Manual....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.T.S. 4000TS Tourniquet Systems Recalled by Zimmer Surgical Inc Due to...
The Issue: Updated on-device label and 3 pages of an updated Operator/Service Manual....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VCLAS (Visualase Cooled Laser Ablation System) Part Number: 9735559...
The Issue: The VCLAS 3mm, 10mm, and 15mm tip devices were not appropriately tested for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iFusion Recalled by Optovue, Inc. Due to FDA determined that a 510(k) is...
The Issue: FDA determined that a 510(k) is needed for the Vault Mapping software (also...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iVue with Normative Database Recalled by Optovue, Inc. Due to FDA determined...
The Issue: FDA determined that a 510(k) is needed for the Vault Mapping software (also...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iVue 500 with iScan Recalled by Optovue, Inc. Due to FDA determined that a...
The Issue: FDA determined that a 510(k) is needed for the Vault Mapping software (also...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by ICU Medical Inc Due to Presence...
The Issue: Presence of Particulate Matter; stainless steel
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydromorphone Hydrochloride Injection Recalled by HOSPIRA INC, LAKE FOREST...
The Issue: Presence of Particulate Matter: Silicone oil
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydromorphone Hydrochloride Injection Recalled by HOSPIRA INC, LAKE FOREST...
The Issue: Presence of Particulate Matter: Silicone oil
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydromorphone Hydrochloride Injection Recalled by HOSPIRA INC, LAKE FOREST...
The Issue: Presence of Particulate Matter: Silicone oil
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acidophilus-Plus Recalled by NatureAll-STF Holding, LLC Due to Undeclared...
The Issue: Undeclared allergens: milk (Colostrum, Dried Yogurt, Whey).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Leci-thin-Plus Recalled by NatureAll-STF Holding, LLC Due to Undeclared...
The Issue: Undeclared allergens: soy (lecithin)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Heart-Plus Recalled by NatureAll-STF Holding, LLC Due to Undeclared Allergens
The Issue: Undeclared allergens: soy (lecithin)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pancreas-Plus Recalled by NatureAll-STF Holding, LLC Due to Undeclared Allergens
The Issue: Undeclared allergens: soy (lecithin)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Thymus Plus Recalled by NatureAll-STF Holding, LLC Due to Undeclared Allergens
The Issue: Undeclared allergens: milk (Colostrum)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Liver-Plus Recalled by NatureAll-STF Holding, LLC Due to Undeclared Allergens
The Issue: Undeclared allergens: soy (lecithin)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Metabo-Plus Recalled by NatureAll-STF Holding, LLC Due to Undeclared Allergens
The Issue: Undeclared allergens: milk (Whey)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Prostate-Plus Recalled by NatureAll-STF Holding, LLC Due to Undeclared Allergens
The Issue: Undeclared allergens: soy (lecithin)
Recommended Action: Do not consume. Return to store for a refund or discard.