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. 1,100 recalls have been distributed to Iowa in the last 12 months.

49,990 total recalls
1,100 in last 12 months

Showing 5941–5960 of 49,990 recalls

FoodApril 17, 2024· Sacramento Cookie Factory

Recalled Item: Original Wine Wafer - Lemon Vanilla [Two sizes: retail package Recalled by...

The Issue: Undeclared allergen (milk)

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 17, 2024· Sacramento Cookie Factory

Recalled Item: Java Wafer - Mocha Hazelnut [Two sizes: retail package of Recalled by...

The Issue: Undeclared allergen (milk)

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 17, 2024· ARG Laboratories, Inc.

Recalled Item: Bull Frog SPF 50 Amphibious Lotion SPF 50 Amphibious Lotion Recalled by ARG...

The Issue: Out of Specification for active ingredient

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 17, 2024· ARG Laboratories, Inc.

Recalled Item: Pain Wizard Recalled by ARG Laboratories, Inc. Due to Out of Specification...

The Issue: Out of Specification for active ingredient. Violative grade of propylene...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 17, 2024· ARG Laboratories, Inc.

Recalled Item: Pain Wizard Recalled by ARG Laboratories, Inc. Due to Out of Specification...

The Issue: Out of Specification for active ingredient. Violative grade of propylene...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 17, 2024· ARG Laboratories, Inc.

Recalled Item: Pain Wizard Recalled by ARG Laboratories, Inc. Due to Out of Specification...

The Issue: Out of Specification for active ingredient. Violative grade of propylene...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 17, 2024· ARG Laboratories, Inc.

Recalled Item: NATURAL PAIN RELIEVING CREAM Recalled by ARG Laboratories, Inc. Due to Out...

The Issue: Out of Specification for active ingredient. Violative grade of propylene...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 17, 2024· ARG Laboratories, Inc.

Recalled Item: NATURAL PAIN RELIEVING CREAM Recalled by ARG Laboratories, Inc. Due to Out...

The Issue: Out of Specification for active ingredient. Violative grade of propylene...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 17, 2024· ARG Laboratories, Inc.

Recalled Item: ALOE GATOR Recalled by ARG Laboratories, Inc. Due to Out of Specification...

The Issue: Out of Specification for active ingredient

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 17, 2024· ARG Laboratories, Inc.

Recalled Item: NATURAL PAIN RELIEVING CREAM Recalled by ARG Laboratories, Inc. Due to Out...

The Issue: Out of Specification for active ingredient. Violative grade of propylene...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 17, 2024· ARG Laboratories, Inc.

Recalled Item: Pain Wizard Recalled by ARG Laboratories, Inc. Due to Out of Specification...

The Issue: Out of Specification for active ingredient. Violative grade of propylene...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 17, 2024· LeMaitre Vascular, Inc.

Recalled Item: Syntel Silicone Thrombectomy Catheter Recalled by LeMaitre Vascular, Inc....

The Issue: The guide tip can become damaged and result in the tip detaching.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2024· YAMAHA MOTOR CORPORATION

Recalled Item: Optical Inspection System Recalled by YAMAHA MOTOR CORPORATION Due to...

The Issue: Non-medical laser products which were determined to not be in compliance...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2024· Fresenius Medical Care Holdings, Inc.

Recalled Item: 2008T BlueStar Hemodialysis Machine Recalled by Fresenius Medical Care...

The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2024· Cardinal Health 200, LLC

Recalled Item: CardinalHealth Curity Flexible Adhesive Bandage X-Large 2 x 3.75 in....

The Issue: Potential contamination of the product with latex adhesive residual.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2024· YAMAHA MOTOR CORPORATION

Recalled Item: Yamaha Surface Mounter YR series Recalled by YAMAHA MOTOR CORPORATION Due to...

The Issue: Non-medical laser products which were determined to not be in compliance...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2024· Fresenius Medical Care Holdings, Inc.

Recalled Item: Blood Pump Rotor Recalled by Fresenius Medical Care Holdings, Inc. Due to An...

The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2024· Fresenius Medical Care Holdings, Inc.

Recalled Item: 2008T BlueStar Hemodialysis Machine Recalled by Fresenius Medical Care...

The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Syringes labeled as: a) SYR 10ML L/L CONTROL Recalled by MEDLINE INDUSTRIES,...

The Issue: These syringes were identified to be affected by the FDA Safety Alert issued...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2024· Integra LifeSciences Corp.

Recalled Item: Integra¿ Cranial access kit (without Prep solutions) Bit and Guard- Recalled...

The Issue: Potential holes and tears in the sterile packaging (header bag) of the...

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

Class II — Potential Health HazardOngoing