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. 2,098 recalls have been distributed to Iowa in the last 12 months.

49,990 total recalls
2,098 in last 12 months

Showing 38613880 of 49,990 recalls

Medical DeviceNovember 6, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline brand Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Surgical Patties & Surgical Strips in specific lots of Custom Convenience...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: DIEP FLAP Convenience kit Recalled by MEDLINE INDUSTRIES, LP - Northfield...

The Issue: Surgical Patties & Surgical Strips in specific lots of Custom Convenience...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: FESS-MB PACK-LF Convenience kit Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Surgical Patties & Surgical Strips in specific lots of Custom Convenience...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2024· Abbott Vascular Inc

Recalled Item: 20/30 INDEFLATOR Recalled by Abbott Vascular Inc Due to Inflation Device...

The Issue: Inflation Device used during cardiovascular procedures may leak in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2024· Abbott Vascular Inc

Recalled Item: 20/30 Priority Pack Kit/.115 RHV Recalled by Abbott Vascular Inc Due to...

The Issue: Inflation Device used during cardiovascular procedures may leak in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline brand Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Surgical Patties & Surgical Strips in specific lots of Custom Convenience...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline brand Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Surgical Patties & Surgical Strips in specific lots of Custom Convenience...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MAJOR NEURO PACK-LF Convenience kit Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Surgical Patties & Surgical Strips in specific lots of Custom Convenience...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline brand Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Surgical Patties & Surgical Strips in specific lots of Custom Convenience...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2024· ICU Medical, Inc.

Recalled Item: ChemoLock Close Vial Spike The Chemolock Closed System Recalled by ICU...

The Issue: Due to finished goods incorrectly packaged and labeled.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2024· Becton Dickinson & Co.

Recalled Item: BD BBL Sensi Disc Ampicillin 2 ¿g (AM-2) - In-Vitro Recalled by Becton...

The Issue: BD identified through potency testing as part of a stability test request to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2024· Microline Surgical, Inc.

Recalled Item: Microscissor Tip (Disposable) Recalled by Microline Surgical, Inc. Due to A...

The Issue: A lot of ReNew Microscissor Tips exhibited a 2% rate of failure in terms of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2024· KCI USA, INC.

Recalled Item: V.A.C. Ulta Therapy Unit & ULTDEV01 The 3M" Recalled by KCI USA, INC. Due to...

The Issue: Due to potential system error alarm and the inability to initiate therapy as...

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

Class II — Potential Health HazardOngoing
DrugNovember 5, 2024· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Hydralazine HCl Tablets Recalled by The Harvard Drug Group LLC dba Major...

The Issue: Failed Impurities/Degradation Specifications; during routine stability...

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

Class III — Low RiskOngoing
Refund
DrugNovember 4, 2024· Boulla LLC

Recalled Item: ZoomMax Capsules Recalled by Boulla LLC Due to Undeclared Sildenafil

The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 4, 2024· Boulla LLC

Recalled Item: ZapMax Capsules Recalled by Boulla LLC Due to Undeclared Sildenafil

The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 4, 2024· Boulla LLC

Recalled Item: VitalityXtra Capsules Recalled by Boulla LLC Due to Undeclared Sildenafil

The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 4, 2024· Boulla LLC

Recalled Item: PeakMax Capsules Recalled by Boulla LLC Due to Undeclared Sildenafil

The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 4, 2024· Yoder's Cashew Crunch

Recalled Item: Hard candy packed in clear plastic bag with gold/red label Recalled by...

The Issue: Undeclared allergen labeling (milk)

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 4, 2024· Yoder's Cashew Crunch

Recalled Item: Yoder's Cashew Crunch Corn Recalled by Yoder's Cashew Crunch Due to...

The Issue: Undeclared allergen labeling (milk)

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

Class II — Potential Health HazardOngoing
Refund