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. 1,937 recalls have been distributed to Missouri in the last 12 months.
Showing 20461–20480 of 29,298 recalls
Recalled Item: UNIQ 1.0: UNIQ FD10 Recalled by Philips Electronics North America...
The Issue: Increase in the failure rate of certain low-voltage DC power supplies (DCPS)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper with release R8.2: Allura Xper FD10 Recalled by Philips...
The Issue: Increase in the failure rate of certain low-voltage DC power supplies ( DCPS )
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neptune Plus (Hemostatic Pad) Recalled by TZ Medical, Inc. Due to Neptune...
The Issue: Neptune Plus was mis-labeled and included the statement WITH ANTIMICROBIAL...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Walrus Arterial Embolectomy Catheter The arterial embolectomy catheter is...
The Issue: Arrow is recalling due to incorrect labeling of products.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The TM Ardis Interbody System implant is a convex Recalled by Zimmer...
The Issue: This field action is being initiated following the firm's discovery of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPHERICAL HEAD (R) 6.5 MM CANCELLOUS SCREW Recalled by Smith & Nephew, Inc....
The Issue: The labels correctly state that the product should be a 25mm screw, but the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard TruGuide Disposable Coaxial Biopsy Needle Mixed Product Part Recalled...
The Issue: May contain two trocar tip stylets with coaxials or two blunt tip stylets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AmediCheck Instant Test Cup Recalled by Branan Medical Corporation Due to...
The Issue: Branan Medical is recalling the AmediCheck Instant Test Cup, a 5 panel drug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RePlant¿ Angled Abutment Part Number 6050-52-60 Recalled by Implant Direct...
The Issue: Issue with design specification; oversized condition.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens RAPIDPoint¿ 500 v2.2.2A Software Upgrade Kit Recalled by Siemens...
The Issue: Some v2.2.2 upgrade kits include a dialysate mode which not cleared/approved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...
The Issue: The surface coating applied to the device is blistering, peeling and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer¿ Air Dermatome II Handpiece Loaner Recalled by Zimmer Surgical Inc...
The Issue: Zimmer Biomet Surgical has received product complaints reporting that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...
The Issue: The surface coating applied to the device is blistering, peeling and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer¿ Air Dermatome II Handpiece w/o Hose Recalled by Zimmer Surgical Inc...
The Issue: The surface coating applied to the device is blistering, peeling and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...
The Issue: The surface coating applied to the device is blistering, peeling and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...
The Issue: The surface coating applied to the device is blistering, peeling and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer¿ Air Dermatome II Handpiece Recalled by Zimmer Surgical Inc Due to...
The Issue: The surface coating applied to the device is blistering, peeling and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...
The Issue: The surface coating applied to the device is blistering, peeling and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OPTICAL BIOMETER AL-Scan: Software Version: 1.09 and earlier. Ophthalmic:...
The Issue: Nidek Inc. received information from our manufacturer NIDEK CO. Japan that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orthopedic manual surgical instrument Usage: Exeter Rasp Handle is a...
The Issue: Malfunctioning of the Exeter Rasp/trial introducer/extractor Handle.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.