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. 2,371 recalls have been distributed to Iowa in the last 12 months.
Showing 41761–41780 of 49,990 recalls
Recalled Item: Life Force Chamber Product Usage:The product is intended for restful...
The Issue: The Life Force chamber is marketed and promoted as a medical device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The STERIS 4085 General Surgical Table Product Usage: is an Recalled by...
The Issue: STERIS engineering analysis has determined the D1 pressure switch in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Patient Data Manager 2.0 (Content manager 2.0 Recalled by Brainlab AG Due to...
The Issue: The following defects have been identified for data loaded with Patient Data...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fentanyl Citrate Injection Recalled by Hospira Inc. Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility: Fliptop vial crimps are loose or missing.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: POLY-TUSSIN AC LIQUID Recalled by Poly Pharmaceuticals, Inc Due to Does Not...
The Issue: Does Not Meet Monograph: Phenylephrine and pseudoephedrine are below...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LORTUSS EX Recalled by Poly Pharmaceuticals, Inc Due to Does Not Meet...
The Issue: Does Not Meet Monograph: Phenylephrine and pseudoephedrine are below...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cephalexin Capsules Recalled by Caraco Pharmaceutical Laboratories, Ltd. Due...
The Issue: CGMP Deviations: These products are being recalled because they were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cephalexin Capsules Recalled by Caraco Pharmaceutical Laboratories, Ltd. Due...
The Issue: CGMP Deviations: These products are being recalled because they were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Affinity¿ Four Birthing Bed Recalled by Hill-Rom, Inc. Due to The attachment...
The Issue: The attachment latch mechanism can become bent depending on user handling....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Esaote PA230E Transducer A portable and cart base ultrasound system Recalled...
The Issue: Using the PA230E transducer with a user-defined setting with the output...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Solanas 2.1mm FIXED DEPTH DRILL Recalled by Alphatec Spine, Inc. Due to...
The Issue: Alphatec Spine is recalling the 2.1mm Fixed Depth Drill 10mm because they...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The synthetic non-absorbable surgical sutures CARDIOFLON Evolution are...
The Issue: A potential splitting of the surface treatment of the thread ends on certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Dental Tapered Screw-Vent Implant Recalled by Zimmer, Inc. Due to...
The Issue: Zimmer Dental is conducting a voluntary recall of a single lot of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The synthetic non-absorbable surgical sutures CARDIOXYL are composed of a...
The Issue: A potential splitting of the surface treatment of the thread ends on certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxygen Mask Recalled by Salter Labs Due to The case label correctly states...
The Issue: The case label correctly states partial rebreather but the insert label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Essential NEO Recalled by Karl Storz Endoscopy Due to KARL STORZ...
The Issue: KARL STORZ Endoscopy-America is recalling the Essential NEO because the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson Cardiology Hemo. McKesson Cardiology" Hemo is intended for complete...
The Issue: McKesson Cardiology Hemo front-end parameter boxes must undergo annual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vitamin B6 Pyridoxine HCL for Injection USP Recalled by Medical Supply...
The Issue: Marketed without an Approved NDA/ANDA; IM and SQ injectable products are...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vitamin B12 Methylcobalamin Injection USP 1000 mcg/ml Recalled by Medical...
The Issue: Marketed without an Approved NDA/ANDA; IM and SQ injectable products are...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Super MIC B Complex for L-Carnitine for Injection USP with Recalled by...
The Issue: Marketed without an Approved NDA/ANDA; IM and SQ injectable products are...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.