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. 2,673 recalls have been distributed to Missouri in the last 12 months.
Showing 7581–7600 of 29,298 recalls
Recalled Item: CAIRE Liberator 45 Recalled by Caire, Inc. Due to An audit discovered some...
The Issue: An audit discovered some inconsistencies in weld penetration on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAIRE Liberator 20 Recalled by Caire, Inc. Due to An audit discovered some...
The Issue: An audit discovered some inconsistencies in weld penetration on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAIRE Liberator 30 Recalled by Caire, Inc. Due to An audit discovered some...
The Issue: An audit discovered some inconsistencies in weld penetration on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAIRE Liberator 45 Recalled by Caire, Inc. Due to An audit discovered some...
The Issue: An audit discovered some inconsistencies in weld penetration on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PAJUNK Continuous Epidural Tray Recalled by Pajunk Medical Systems, L.P. Due...
The Issue: The tray contains a 2ml ampule of 0.75% Marcaine Spinal in lieu of a 10ml...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORISE Gel Submucosal Lifting Agent--Indicated for use in gastrointestinal...
The Issue: ***Update12/13/22***:Product removal due to higher incidence of adverse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORISE Gel Syringe Submucosal Lifting Agent Kits: indicated for use Recalled...
The Issue: ***Update12/13/22***:Product removal due to higher incidence of adverse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORISE ProKnife Procedure Kits: indicated for use in gastrointestinal...
The Issue: ***Update12/13/22***:Product removal due to higher incidence of adverse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FERNO POWER X1 AMBULANCE COT- Item #0015807/UDI-DI 00190790002183 with 36V...
The Issue: Batteries could become unstable when not properly maintained and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fogarty Arterial Embolectomy Catheters Model Number: 120602FP 120403FP...
The Issue: Due to an increase of confirmed latex deterioration complaints for arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fogarty Biliary Balloon Probes Model Number: 410235FP 410405FP 410236FP...
The Issue: Due to an increase of confirmed latex deterioration complaints for arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NaturaLyte Liquid Acid concentrate Recalled by Fresenius Medical Care...
The Issue: The "Nominal Chemical Composition" section of the label incorrectly lists...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan autoSCAN-4 Instrument Recalled by Beckman Coulter, Inc. Due to Due...
The Issue: Due to MicroScan autoSCAN-4 Instruments being manufactured with an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Multitest 6-Color TBNK with optional BD Trucount Tubes (Cat. No. 662995)...
The Issue: Due to partial label detachment on tubes. This can cause tubes to become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Trucount Tubes (Cat. No. 663028) Recalled by Becton, Dickinson and...
The Issue: Due to partial label detachment on tubes. This can cause tubes to become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blinq Pediatric Vision Scanner-Pediatric Vision Scanner-intended for...
The Issue: Unable to charge the battery pack- battery packs will allow the batteries to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Trucount Tubes (Cat. No. 340334) Recalled by Becton, Dickinson and...
The Issue: Due to partial label detachment on tubes. This can cause tubes to become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EMBLEM MRI S-ICD Recalled by Boston Scientific Corporation Due to There is...
The Issue: There is an incorrect manufacturing date/timestamp within the software which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE DENTAL PACK Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...
The Issue: Medline received complaints on some of the breather pouches with in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CENTURION MEDICAL PRODUCTS NICU PICC INSERTION BUNDLE W/O Recalled by...
The Issue: Medline received complaints on some of the breather pouches with in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.