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. 1,073 recalls have been distributed to Iowa in the last 12 months.
Showing 12921–12940 of 49,990 recalls
Recalled Item: 23.4% Sodium Chloride Injection Recalled by The Ritedose Corporation Due to...
The Issue: Labeling: Incorrect Barcode: Product barcode incorrectly identifies the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Esomeprazole Magnesium Delayed-Release Capsules Recalled by Mylan...
The Issue: Failed Impurities/Degradation Specifications: OOS result was obtained for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cequa (cyclosporine ophthalmic solution) 0.09% Recalled by SUN...
The Issue: Subpotent Drug and Presence of Particulate Matter: low out-of-specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to...
The Issue: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium and Hydrochlorothiazide Tablets USP Recalled by Lupin...
The Issue: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to...
The Issue: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium and Hydrochlorothiazide Tablets USP Recalled by Lupin...
The Issue: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium and Hydrochlorothiazide Tablets USP Recalled by Lupin...
The Issue: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to...
The Issue: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Janumet (sitagliptin and metformin HCl) tablets Recalled by MERCK SHARP &...
The Issue: Presence of foreign substance: Presence of stainless steel particulates in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Olympus DISPOSABLE GRASPING FORCEPS Recalled by Olympus Corporation of the...
The Issue: Forceps do not comply with Olympus standards for the amount of force...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cooper Surgical H/S ELLIPTOSPHERE CATH 5 Fr -For administering contrast...
The Issue: Incorrect bonding material used for assembly of the catheter, may fail,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cooper Surgical H/S ELLIPTOSPHERE CATH 5 FR Set-For administering contrast...
The Issue: Incorrect bonding material used for assembly of the catheter, may fail,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CooperSurgical H/S CATHETER SET FR 5 with Integated Stylet Model: Recalled...
The Issue: Incorrect bonding material used for assembly of the catheter, may fail,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Evans Wedge Disposable Trials Recalled by restor3d Inc. Due to During...
The Issue: During re-work of disposable instruments to relabel for 4-year shelf-life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triathlon Tritanium Tibial Component (Size 6) Recalled by Howmedica...
The Issue: Stryker has discovered a potential product mix where the size of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanta INS Implantable Neurostimulator. Medtronic Model 977006 Vanta with...
The Issue: The Implantable Neurostimulator Model may be susceptible to not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percept PC BrainSense Implantable Neurostimulator (INS) Model B35200...
The Issue: The Implantable Neurostimulator (INS) cannot communicate with the clinical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invacare TDX SP2 Recalled by Invacare Corporation Due to The battery wiring...
The Issue: The battery wiring harness on affected wheelchairs may become disconnected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroMARK Breast Biopsy Marker Recalled by Devicor Medical Products Inc Due...
The Issue: Small patient labels do not match the primary device label. The primary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.