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. 2,644 recalls have been distributed to Iowa in the last 12 months.
Showing 4361–4380 of 49,990 recalls
Recalled Item: SURG STRP 3X6 Model/Catalog Number: 801456. The surgical patties and...
The Issue: Identified higher-than-expected levels of endotoxin within the raw material...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SURG PAT XRAY 1/4X3 Model/Catalog Number: 801398. The surgical patties...
The Issue: Identified higher-than-expected levels of endotoxin within the raw material...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SURG STRP 3-1/2X6 Model/Catalog Number:801457. The surgical patties and...
The Issue: Identified higher-than-expected levels of endotoxin within the raw material...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SURG PAT XRAY 1/2X1 Model/Catalog Number: 801402. The surgical patties...
The Issue: Identified higher-than-expected levels of endotoxin within the raw material...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SURG STRP 1X6-200 Model/Catalog Number: 801453. The surgical patties and...
The Issue: Identified higher-than-expected levels of endotoxin within the raw material...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICR PATIE RND Model/Catalog Number: 801396. CODMAN Surgical Patties and...
The Issue: Identified higher-than-expected levels of endotoxin within the raw material...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SURG PAT XRAY 1/4X1-1/2 Model/Catalog Number: 801397. The surgical patties...
The Issue: Identified higher-than-expected levels of endotoxin within the raw material...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SURG PAT XRAY 1/2X3 Model/Catalog Number: 801407. The surgical patties...
The Issue: Identified higher-than-expected levels of endotoxin within the raw material...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SURG STRP 1/4X6 Model/Catalog Number: 801450. The surgical patties and...
The Issue: Identified higher-than-expected levels of endotoxin within the raw material...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SURG PAT XRAY 1X1 Model/Catalog Number: 801403. The surgical patties...
The Issue: Identified higher-than-expected levels of endotoxin within the raw material...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lactaid Lactose Reduced milk 1. 96 oz Lactaid Whole Milk Recalled by HP Hood...
The Issue: Milk may contain undeclared almond from almond milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Veklury (remdesivir) for injection Recalled by Gilead Sciences, Inc. Due to...
The Issue: Presence of Particulate Matter: Presence of glass particle.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Chameleon PTA Balloon Catheter with Injection Port 5mm x 40mm Recalled by...
The Issue: Specific lots of the Chameleon PTA Balloon Catheter failed to meet in-house...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AD-TECH Spencer Probe Depth Electrode Recalled by Ad-Tech Medical Instrument...
The Issue: Ad-Tech is recalling these A-Style SD Depth Electrodes because a label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AD-TECH Spencer Probe Depth Electrode Recalled by Ad-Tech Medical Instrument...
The Issue: Ad-Tech is recalling these A-Style SD Depth Electrodes because a label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AD-TECH Spencer Probe Depth Electrode Recalled by Ad-Tech Medical Instrument...
The Issue: Ad-Tech is recalling these A-Style SD Depth Electrodes because a label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EVIS EXERA III Gastrointestinal Videoscope GIF-1TH190 Product...
The Issue: To better define the drying procedures described in the IFU to improve the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Recharger Kits Recalled by Medtronic Neuromodulation Due to The...
The Issue: The Wireless Rechargers in the kits may be unable to enter a recharging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Americot 20-01S (1/4" x 1/4") or 6mm x 6mm: Neurological Recalled by...
The Issue: Product defect where the X-ray detectable barium strip (aka radio-opaque...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nihon Kohden Adult Ear Clip SpO2 Sensor Recalled by Nihon Kohden America Inc...
The Issue: Due to oximeters not having FDA market approval or clearance to distribute...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.