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. 1,080 recalls have been distributed to Missouri in the last 12 months.
Showing 12321–12340 of 52,570 recalls
Recalled Item: NaviCare Nurse Call/Voalte Nurse Call Recalled by Baxter Healthcare...
The Issue: An issue has been identified with Phillips (Emergin) and Longleaf non relay...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSSUR VARIFLEX SUBA JUNIOR foot and ankle external prosthesis Recalled by...
The Issue: Due to receiving complaints related to broken (cracked) prosthetic foot with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Avance CS2 Recalled by GE Healthcare, LLC Due to The base of...
The Issue: The base of the anesthesia system can have a crack and could potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEAD 3387S-40 STIMLOC DBS Recalled by Medtronic Neuromodulation Due to There...
The Issue: There are a small number of units of the DBS Lead with StimLoc kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HammerTube Implant Recalled by Paragon 28, Inc. Due to Due to Titanium...
The Issue: Due to Titanium plasma coating not present implant.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOLTIVE SuperPulsed Laser Fibers Recalled by Olympus Corporation of the...
The Issue: Device model and size for affected lots of Laser Fibers may be mismatched...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anti-SARS-CoV-2 IgG Quantitative Reagent Pack- Intended for use on VITROS¿...
The Issue: On-Analyzer Stability (OAS) time, supported for 6 weeks; not 8 weeks as is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rich s Milk Chocolate Giant Layered Peanut Butter and Cups Recalled by...
The Issue: Salmonella. Product made using recalled Jif peanut butter
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ortiga mas Ajo Rey con Omega 3 Recalled by Amazon.com, Inc. Due to...
The Issue: Marketed Without An Approved NDA/ANDA: FDA laboratory analysis found the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Artri Ajo King con Ortiga y Omega 3 tablets Recalled by Amazon.com, Inc. Due...
The Issue: Marketed Without An Approved NDA/ANDA: FDA laboratory analysis found the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Artri King con Ortiga y Omega 3 tablets Recalled by Amazon.com, Inc. Due to...
The Issue: Marketed Without An Approved NDA/ANDA: FDA laboratory analysis found the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: a. DYNAREX WeCare PETROLATUM JELLY Recalled by Mckesson Medical-Surgical...
The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: a. Dynarex DRESSING Recalled by Mckesson Medical-Surgical Inc. Corporate...
The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: a. INTEGRA LIFESCIENCE (WND CARE) Shur-Conform Oil Emulsion Oil Emulsion...
The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MERIT MEDICAL SYSTEMS StayFIX FIXATION DEVICE Recalled by Mckesson...
The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: a. DERMA SCIENCES Recalled by Mckesson Medical-Surgical Inc. Corporate...
The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Monitoring Set Recalled by Cook Incorporated Due to The products...
The Issue: The products may contain excess coating material on the outside and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: a. TIDI PRODUCTS Recalled by Mckesson Medical-Surgical Inc. Corporate Office...
The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: a. Alcon Clear Care Contact Lens Solution Clear Care 12 oz. Solution...
The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dynarex SWAB Recalled by Mckesson Medical-Surgical Inc. Corporate Office Due...
The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.