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. 2,409 recalls have been distributed to Iowa in the last 12 months.
Showing 38281–38300 of 49,990 recalls
Recalled Item: Navigation System II-Cart Recalled by Stryker Instruments Div. of Stryker...
The Issue: Stryker initiated a device recall of the Navigation System II-Cart, Camera...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remel Blood Agar (TSA w/sheep blood) plate packaged Recalled by Remel Inc...
The Issue: Product may be contaminated with Listeria monocytogenes.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synovis VASCU-GUARD Peripheral Vascular Patch in the following sizes and...
The Issue: Baxter healthcare is recalling specific product codes of Vascu-Guard...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wheel caster set screw for Ferno iNX Wheeled Stretcher. Ferno Recalled by...
The Issue: The firm discovered an improperly installed set screw in one caster arm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra¿ Long Epidural Steroid Injection Needle (Tuohy Needle) Recalled by...
The Issue: Integra LifeSciences Corp. d.b.a. Integra Pain Management Announces...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI Custom Eyes¿ Ophthalmic Procedure Kits with the component -Devon...
The Issue: Devon Light Glove in procedure kits may have holes/slits compromising...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI Custom Eyes¿ Ophthalmic Procedure Kits with the component -Devon...
The Issue: Devon Light Glove in procedure kits may have holes/slits compromising...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI Custom Eyes¿ Ophthalmic Procedure Kits with the component -Devon...
The Issue: Devon Light Glove in procedure kits may have holes/slits compromising...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI Custom Eyes¿ Ophthalmic Procedure Kits with the component -Devon...
The Issue: Devon Light Glove in procedure kits may have holes/slits compromising...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI Custom Eyes¿ Ophthalmic Procedure Kits with the component -Devon...
The Issue: Devon Light Glove in procedure kits may have holes/slits compromising...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Unilateral external fixation ankle clamp Product Usage: Unilateral external...
The Issue: Ankle clamp was assembled incorrectly; the offset of the pin to the pivot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Base for Terumo Advanced Perfusion System 1 Recalled by Terumo...
The Issue: Terumo CVS is implementing field correction activities to address the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 100/120V AC Recalled by Terumo Cardiovascular Systems Corporation Due to...
The Issue: Terumo CVS is implementing field correction activities to address the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sodium Sulfacetamide 9% and Sulfur 4.5% Wash Kit Recalled by Mission...
The Issue: Microbial Contamination of Non-Sterile Products: Product failed USP...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sodium Sulfacetamide 9% and Sulfur 4.5% Wash Kit with Sunscreen Recalled by...
The Issue: Microbial Contamination of Non-Sterile Products: Product failed USP...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ULTRA-FAST FIX Knot Pusher Suture Cutters Product Number: 72201537 Intended...
The Issue: Sterility of device maybe compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: I-Portal¿ NOTC and VNG Recalled by Neuro Kinetics, Inc. Due to complaints of...
The Issue: complaints of system malfunction and unintended, sudden movement at start...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRI Femoral Impactor Block for knee prosthesis surgery. Orthopedic Manual...
The Issue: Potential for uncured adhesive between the metal threaded insert and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azithromycin Tablets Recalled by PD-Rx Pharmaceuticals, Inc. Due to cGMP...
The Issue: cGMP Deviations: This recall is a result of the original manufacturer's...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Azithromycin 500 mg tablets Recalled by PD-Rx Pharmaceuticals, Inc. Due to...
The Issue: cGMP Deviations: This recall is a result of the original manufacturer's...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.