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. 1,069 recalls have been distributed to Iowa in the last 12 months.

49,990 total recalls
1,069 in last 12 months

Showing 16221–16240 of 49,990 recalls

DrugMarch 22, 2021· Macleods Pharma Usa Inc

Recalled Item: Candesartan Cilexetil Tablets Recalled by Macleods Pharma Usa Inc Due to...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugMarch 22, 2021· Novo Nordisk Inc

Recalled Item: TRESIBA (insulin degludec injection) 100 units/mL (U-100) Recalled by Novo...

The Issue: Temperature Abuse: product samples were stored at temperatures below 32* F...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 22, 2021· Novo Nordisk Inc

Recalled Item: ViCTOZA (liraglutide) injection Recalled by Novo Nordisk Inc Due to...

The Issue: Temperature Abuse: product samples were stored at temperatures below 32* F...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 22, 2021· Novo Nordisk Inc

Recalled Item: NovoLog FlexPen (insulin aspart) Injection Recalled by Novo Nordisk Inc Due...

The Issue: Temperature Abuse: product samples were stored at temperatures below 32* F...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 22, 2021· Novo Nordisk Inc

Recalled Item: Saxenda (liraglutide) Injection Recalled by Novo Nordisk Inc Due to...

The Issue: Temperature Abuse: product samples were stored at temperatures below 32* F...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 22, 2021· Simply Delicious Inc.

Recalled Item: Bobo's Maple Pecan Oat Bars Recalled by Simply Delicious Inc. Due to Two...

The Issue: Two consumer complaints were received for peanuts in maple pecan bars.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodMarch 22, 2021· Land O'Lakes, Inc.

Recalled Item: Land O Lakes Queso Bravo White Cheese Dip with Jalapeno Recalled by Land...

The Issue: Queso Cheese dip may contain foreign material (metal).

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodMarch 20, 2021· Avanti Frozen Foods Private Limited

Recalled Item: 365 Whole Foods Market Farm Raised Cooked Shrimp 2 lbs/Ready- Recalled by...

The Issue: One lot of uncooked shrimp was inadvertently packaged as cooked shrimp.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 19, 2021· Cardiac Assist, Inc

Recalled Item: Protek Solo Venous Dilator Set: dilator Recalled by Cardiac Assist, Inc Due...

The Issue: On 02/26/2021, it was found that there were incorrectly packaged Dilator...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2021· Aesculap Implant Systems LLC

Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NL476...

The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2021· Aesculap Implant Systems LLC

Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NO180Z...

The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2021· Aesculap Implant Systems LLC

Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NL494...

The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2021· Aesculap Implant Systems LLC

Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NO156Z...

The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2021· Aesculap Implant Systems LLC

Recalled Item: Univation X System Tray Sysem knee implant devices as follows: Recalled by...

The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2021· Aesculap Implant Systems LLC

Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NL488...

The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2021· Aesculap Implant Systems LLC

Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NL482...

The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2021· Baxter Healthcare Corporation

Recalled Item: Spectrum IQ - Infusion Pump - Product Usage: intended to Recalled by Baxter...

The Issue: Potentially defective component in the AC power adapter which may fail over...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2021· Aesculap Implant Systems LLC

Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NL470...

The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2021· GE Healthcare, LLC

Recalled Item: Revolution CT Recalled by GE Healthcare, LLC Due to GE Healthcare has become...

The Issue: GE Healthcare has become aware of a potential issue on the Revolution CT...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2021· Cytocell Ltd.

Recalled Item: Chromosome X Alpha-Satellite in FITC Spectrum - Product Usage: Analyte...

The Issue: Users may observe additional locus specific signals at 9q34. The device pack...

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

Class II — Potential Health HazardOngoing