Product Recalls in Missouri
Product recalls affecting Missouri — including food, drugs, consumer products, medical devices, and vehicles distributed to Missouri. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,715 recalls have been distributed to Missouri in the last 12 months.
Showing 301–320 of 52,570 recalls
Recalled Item: Meijer STERILE saline wound wash Recalled by Medline Industries, LP Due to...
The Issue: Medline has identified that the manufacturer of the sterile saline wound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Sterile Saline Wound Wash Recalled by Medline Industries, LP Due to...
The Issue: Medline has identified that the manufacturer of the sterile saline wound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Convenience Kits: 1) TRUNK KIT W/EXPIRATION Recalled by Medline...
The Issue: Medline has identified that the manufacturer of the sterile saline wound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Convenience Kits: 1) NAIL KIT Recalled by Medline Industries, LP Due...
The Issue: Medline has identified that the manufacturer of the sterile saline wound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK 2 Gram-negative Susceptibility Cards Containing o Polymyxin B (pb02n)...
The Issue: Potential risk of Quality Control failures and/or false resistant antibiotic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EMPOWR 3D Knee Tibial Insert 5R 14MM Recalled by Encore Medical, LP Due to...
The Issue: 942-01-40G acetabular system package was found to contain 942-01-36H...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EMPOWR Acetabular System: Liner Recalled by Encore Medical, LP Due to...
The Issue: 942-01-40G acetabular system package was found to contain 942-01-36H...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lanreotide Injection Recalled by Cipla USA, Inc. Due to Presence of...
The Issue: Presence of Particulate Matter.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Halyard TRANSPORT BAG KIT. Kit Code: LIFE0080-01. Recalled by AVID Medical,...
The Issue: Tyvek bag seal issue which may compromise sterility of the kit.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATEC Lateral Navigation Disc Prep Instruments LIF NAV Recalled by Alphatec...
The Issue: Due a design issue where the navigated array connection geometry is incorrect.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATEC Lateral Navigation Disc Prep Instruments LIF NAV Recalled by Alphatec...
The Issue: Due a design issue where the navigated array connection geometry is incorrect.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioGlo Fluorescein Sodium Ophthalmic Strips USP Recalled by Wizcure Pharmaa...
The Issue: Lack of Assurance of Sterility: Products have not been manufactured in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bio Glo Fluorescein Sodium Ophthalmic Strips USP Recalled by Wizcure Pharmaa...
The Issue: Lack of Assurance of Sterility: Products have not been manufactured in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vista Tears Polyethylene Glycol 400 0.4% w/v Recalled by Wizcure Pharmaa...
The Issue: Lack of Assurance of Sterility: Products have not been manufactured in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vista Gel Hypromellose USP 0.3% w/v Recalled by Wizcure Pharmaa Private...
The Issue: Lack of Assurance of Sterility: Products have not been manufactured in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vista Gonio Eye Lubricant Recalled by Wizcure Pharmaa Private Limited Due to...
The Issue: Lack of Assurance of Sterility: Products have not been manufactured in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vista Meibo Tears Propylene Glycol 0.6% w/v Eye Drops Advanced Recalled by...
The Issue: Lack of Assurance of Sterility: Products have not been manufactured in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CHNaO Fluorescein Sodium Ophthalmic Strips Recalled by Wizcure Pharmaa...
The Issue: Lack of Assurance of Sterility: Products have not been manufactured in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets Recalled by Alvogen, Inc Due to Product Mix-Up:...
The Issue: Product Mix-Up: A single bottle of this lot was reported by a pharmacy to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rosuvastatin Tablets Recalled by AvKARE Due to Out of specification for...
The Issue: Out of specification for dissolution.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.