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. 2,447 recalls have been distributed to Iowa in the last 12 months.

49,990 total recalls
2,447 in last 12 months

Showing 2846128480 of 49,990 recalls

DrugJuly 26, 2017· HOSPIRA INC, LAKE FOREST

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.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2017· ICU Medical Inc

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.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2017· HOSPIRA INC, LAKE FOREST

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.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 26, 2017· NatureAll-STF Holding, LLC

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.

Class I — Serious Health HazardOngoing
Refund
FoodJuly 26, 2017· NatureAll-STF Holding, LLC

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.

Class I — Serious Health HazardOngoing
Refund
FoodJuly 26, 2017· NatureAll-STF Holding, LLC

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.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 26, 2017· NatureAll-STF Holding, LLC

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.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 26, 2017· NatureAll-STF Holding, LLC

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.

Class I — Serious Health HazardOngoing
Refund
FoodJuly 26, 2017· NatureAll-STF Holding, LLC

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.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 26, 2017· NatureAll-STF Holding, LLC

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.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 26, 2017· NatureAll-STF Holding, LLC

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.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 25, 2017· Teva Pharmaceuticals USA

Recalled Item: Albuterol Sulfate Inhalation Solution Recalled by Teva Pharmaceuticals USA...

The Issue: Failed Impurities/Degradation Specifications: high out of specification...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJuly 25, 2017· Arrow International Inc

Recalled Item: ARROW PICC powered by ARROW VPS Stylet Recalled by Arrow International Inc...

The Issue: Finished good kits may contain incorrect components. Kits that should...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2017· Siemens Medical Solutions USA, Inc.

Recalled Item: Syngo Imaging version V31 (model # 10014063) is a Picture Recalled by...

The Issue: Siemens is releasing a letter to inform about potential data loss relevant...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2017· Arrow International Inc

Recalled Item: ArrowADVANTAGE 5 Pressure Injectable Peripherally Inserted Central Catheter...

The Issue: Finished good kits may contain incorrect components. Kits that should...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2017· Sorin Group Italia SRL - CRF

Recalled Item: Platinium CRT DF1 1711 Recalled by Sorin Group Italia SRL - CRF Due to There...

The Issue: There is a possibility of overconsumption of certain PLATINIUM Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2017· Epimed International

Recalled Item: COUDE Blunt Nerve Block Needle Recalled by Epimed International Due to...

The Issue: Potential for partially incomplete seal of product, impacting sterility.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2017· Epimed International

Recalled Item: TUOHY Epidural Needle Recalled by Epimed International Due to Potential for...

The Issue: Potential for partially incomplete seal of product, impacting sterility.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2017· Sorin Group Italia SRL - CRF

Recalled Item: Platinium VR DF4 1240 Recalled by Sorin Group Italia SRL - CRF Due to There...

The Issue: There is a possibility of overconsumption of certain PLATINIUM Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2017· Sorin Group Italia SRL - CRF

Recalled Item: Platinium CRT-D 1741 Recalled by Sorin Group Italia SRL - CRF Due to There...

The Issue: There is a possibility of overconsumption of certain PLATINIUM Implantable...

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

Class II — Potential Health HazardOngoing