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. 1,723 recalls have been distributed to Iowa in the last 12 months.
Showing 45621–45640 of 49,990 recalls
Recalled Item: Stryker Oasys Midline Occiput Plate-1) Small 2) Medium 3) Large Recalled by...
The Issue: Stryker has received reports from customers indicating post-operative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEO-MED ORTHO TOTAL JOINT TRACECART(R) Recalled by DeRoyal Industries Inc...
The Issue: DeRoyal recalled kits that contained Stryker togas which were recalled for a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Glidesheath (tm) Recalled by Terumo Medical Corporation Due to...
The Issue: Medical devices were incorrectly labeled with extended expiration dates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ******APEX Arthroscopy Tubing Set. Intended for use for joint Recalled by...
The Issue: Conmed Linvatec received complaints that their products C7120 APEX...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TotalCare Bed used with AccuMax Quantum VPC mattress AccuMax Quantum...
The Issue: When the bed is put into the chair egress position, the magnets on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pinnacle¿ Destination¿ Peripheral Guiding Sheath Recalled by Terumo Medical...
The Issue: Medical devices were incorrectly labeled with extended expiration dates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ******QTY 1***APEX Arthroscopy Tubing Set. Intended for use for Recalled by...
The Issue: Conmed Linvatec received complaints that their products C7120 APEX...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens MEVATRON series Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: The information regarding the FILM Mode calibration may have been considered...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: R3 (TM) XLPE ACETABULAR LINER UHMWPE Recalled by Smith & Nephew Inc Due to...
The Issue: One batch of 60 mm 20o R3 XLPE liner may be laser etched and packaged as a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: R3 (TM) XLPE ACETABULAR LINER UHMWPE Recalled by Smith & Nephew Inc Due to...
The Issue: One batch of 60 mm 20o R3 XLPE liner may be laser etched and packaged as a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atropine Sulfate 50 mg/ml Injection Recalled by Lowlite Investments, Inc....
The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dexpanthenol 250 mg/ml Injection Recalled by Lowlite Investments, Inc. D/B/A...
The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluphenazine 25 mg/ml Injection Recalled by Lowlite Investments, Inc. D/B/A...
The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Guanabenz 8 mg/ml Injection Recalled by Lowlite Investments, Inc. D/B/A...
The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diphenhydramine 50 mg/ml Injection Recalled by Lowlite Investments, Inc....
The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phentolamine 20 mg/ml Injection Recalled by Lowlite Investments, Inc. D/B/A...
The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sodium Iodide 20% Injection Recalled by Lowlite Investments, Inc. D/B/A...
The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methylprednisolone Acetate 80 mg/ml Injection Recalled by Lowlite...
The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hippiron 20 mg/ml Injection Recalled by Lowlite Investments, Inc. D/B/A...
The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cal-Phos 1000 Injection Recalled by Lowlite Investments, Inc. D/B/A Olympia...
The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.