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. 1,020 recalls have been distributed to Missouri in the last 12 months.
Showing 24281–24300 of 52,570 recalls
Recalled Item: Durex Pleasure Pack (60 ct) Recalled by Reckitt Benckiser LLC Due to Five...
The Issue: Five batches of the product have failed the specification of 1.0kPa for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fungitell Kit Recalled by Associates of Cape Cod, Inc. Due to The kits may...
The Issue: The kits may contain the incorrect number of components or the kits may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stingray" Guidewire Recalled by Boston Scientific Corporation Due to A batch...
The Issue: A batch of 185cm Stingray Guidewires are incorrectly labeled as 300cm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemotherm CE Dual Reservoir Cooler/Heater Recalled by Cincinnati Sub-Zero...
The Issue: Evidence supports that when customers performed a fuse replacement as part...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olmesartan Medoxomil and Hydrochlorothiazide Tablets Recalled by Teva...
The Issue: Failed dissolution specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cochlear Baha 5 Sound Processor Tamper Proof Battery Door (3 pcs.) Recalled...
The Issue: Product was packaged with the Incorrect tamper proof battery door.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omnipod DASH Insulin Management System Recalled by Insulet Corporation Due...
The Issue: There is a potential for a communication interruption following a bolus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: J Type Bone Marrow Needle 13ga x 6cm - Product Recalled by Angiotech (Manan...
The Issue: Argon Medical has identified an internal manufacturing issue on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aguja para Biopsia Tipo Medula Osea Ergonomica 11ga x 10cm Recalled by...
The Issue: Argon Medical has identified an internal manufacturing issue on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aguja de Aspiracion con Profundidad Ajustable Tipo I 16ga x Recalled by...
The Issue: Argon Medical has identified an internal manufacturing issue on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aguja de Aspiration con Profundidad Ajustable Tipo I 15ga x Recalled by...
The Issue: Argon Medical has identified an internal manufacturing issue on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: J Type Bone Marrow Needle 13ga x 10 cm- Product Recalled by Angiotech (Manan...
The Issue: Argon Medical has identified an internal manufacturing issue on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: "J" Type Bone Marrow Needle 11ga x 10 cm - Recalled by Angiotech (Manan...
The Issue: Argon Medical has identified an internal manufacturing issue on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Double Diamond J Type Bone Marrow Needle & Marrow Extraction Recalled by...
The Issue: Argon Medical has identified an internal manufacturing issue on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERMA-HAND Silk Suture Size 5 Recalled by Ethicon, Inc. Due to The sutures...
The Issue: The sutures inside the packaging are not the same size or type as indicated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PREMIER Cryptococcal Antigen Recalled by Meridian Bioscience Inc Due to An...
The Issue: An enzyme reagent included in the kit is not maintaining stability through...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus PCF-Q180AC Video Colonoscope - Product Usage: These endoscopes are...
The Issue: The adhesive used in the repair of the endoscope was incorrectly prepared....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anti-HAV IgM test System Recalled by Roche Diagnostics Corporation Due to...
The Issue: Potential for erroneous result messages for the Anti-HAV IgM assay when run...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tina-quant IgM Gen.2 Recalled by Roche Diagnostics Corporation Due to New...
The Issue: New endogenous interference claims have been established for the following...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lactate Gen.2 Recalled by Roche Diagnostics Corporation Due to New...
The Issue: New endogenous interference claims have been established for the following...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.