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. 1,905 recalls have been distributed to Missouri in the last 12 months.
Showing 23821–23840 of 29,298 recalls
Recalled Item: BD 10 mL Syringe BD Luer-Lok Tip with Blunt Plastic Cannula Recalled by...
The Issue: The stopper of the 10mL BD Luer-Lok syringe is not properly seated in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINAC Accelerators: ARTISTE Recalled by Siemens Medical Solutions USA, Inc...
The Issue: A hardware update to replace the old PCB Assembly, Head Driver-G41 with PCB...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quickie Q7 Adult Rigid Wheelchair Model EIR4. Recalled by Sunrise Medical...
The Issue: There is the potential for the height adjustable handle to dislodge due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HEPFLUSH-10 (HEPARIN LOCK FLUSH SOLUTION Recalled by Fresenius Kabi USA, LLC...
The Issue: The lot failed pH specification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CD8 (Leu-2a) PE (In vitro diagnostic) Recalled by BD Biosciences, Systems &...
The Issue: One lot of CD8 PE is contaminated with CD4 FITC and may cause an unexpected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anti-Lambda APC-H7 Recalled by BD Biosciences, Systems & Reagents Due to Two...
The Issue: Two lots of the Anti-Lambda APC-H7 antibody are contaminated with CD38 antibody.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: lnline Persuader- PedFuse Pedicle Screw System Recalled by SpineFrontier,...
The Issue: A crack may develop in the handle to the Inline Persuader, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femto LDV Z-Generation Femtosecond Surgical Lasers are used to perform...
The Issue: The devices were not shipped with the Starter Kits.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merlin@home RF Remote Monitoring Transmitter Recalled by St Jude Medical...
The Issue: Transmitter may initiate a software reset resulting in backup operation in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobas b 221 (versions 5 and 6) Blood Gas and Electrolytes Analyzer Recalled...
The Issue: Chemical component of the F3 Fluid pack and environmental bacterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ti-Bond Marketing Literature/Labeling Recalled by Spinal Elements, Inc Due...
The Issue: Spinal Elements is recalling the Ti-Bond related brochures that includes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The XN-Series modules (XN-10 Recalled by Sysmex Corporation Due to There is...
The Issue: There is a potential for elevated hemoglobin (Hgb) and impedance platelet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Metasul Femoral Head - indicated for total hip arthroplasty for Recalled by...
The Issue: Potential compromise of the inner sterile tray. If a compromised tray is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDPOR TITAN MAX Orbital Floor and Wall (OFW) MEDPOR-Titanium-Barrier (MTB)...
The Issue: Article #81036 (MEDPOR Titan Max OFW - MTB - Right) reportedly contained...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDPOR Surgical Implant Contoured Two Piece Chin 5 mm Recalled by Stryker...
The Issue: Potential for implant damage, implant cracking off/breaking intra-operatively.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDPOR BARRIER Sheets Rectangle Product Usage: MEDPOR Implants in block...
The Issue: Potential for implant deformation, implant mechanical stability too low,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apollo (cold) Laser Desktop Control Units Recalled by Pivotal Health...
The Issue: Control units were equipped with an internal mounting kit that does not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDPOR BARRIER Sheets Orbital Floor Implant Product Usage: MEDPOR Implants...
The Issue: Potential for implant deformation, implant mechanical stability too low,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoCr Femoral Head - A modular head component is used Recalled by Zimmer Gmbh...
The Issue: Potential compromise of the inner sterile tray. If a compromised tray is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biolox Delta Femoral Head - The BIOLOX delta Ceramic Femoral Recalled by...
The Issue: Potential compromise of the inner sterile tray. If a compromised tray is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.