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. 1,111 recalls have been distributed to Missouri in the last 12 months.
Showing 7121–7140 of 29,298 recalls
Recalled Item: MobiCT-32 AIRO Mobile CT Scanner Recalled by Mobius Imaging, LLC Due to...
The Issue: Stryker received one report of an injury to an untrained user that occurred...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgical convenience kits labeled as: CENTURION MEDICAL PRODUCTS...
The Issue: The recall is due to the perforated bag not allowing for outside of the kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Identity Shoulder System Resection Planer 35mm Resection Planer Recalled by...
The Issue: Two planers were found to be unusable during sawbones shoulder training.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Option Stemmed Tibial Component Size 7 Recalled by Zimmer, Inc. Due...
The Issue: Zimmer Biomet is conducting a voluntary medical device recall related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Option Stemmed Tibial Component Size 5 Recalled by Zimmer, Inc. Due...
The Issue: Zimmer Biomet is conducting a voluntary medical device recall related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Option Stemmed Tibial Component Size 4 Recalled by Zimmer, Inc. Due...
The Issue: Zimmer Biomet is conducting a voluntary medical device recall related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Option Stemmed Tibial Component Size 6 Recalled by Zimmer, Inc. Due...
The Issue: Zimmer Biomet is conducting a voluntary medical device recall related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Option Stemmed Tibial Component Size 8 Recalled by Zimmer, Inc. Due...
The Issue: Zimmer Biomet is conducting a voluntary medical device recall related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Option Stemmed Tibial Component Size 3 Recalled by Zimmer, Inc. Due...
The Issue: Zimmer Biomet is conducting a voluntary medical device recall related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Turbett Surgical Container Recalled by Turbett Surgical, Inc. Due to Pod may...
The Issue: Pod may have weld failures breaching the sterile barrier and result in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invisalign Express 10 Invisalign System Comprehensive Recalled by Align...
The Issue: 3D orthodontic planning software has a defect that leads to an issue where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Turbett Surgical Container Recalled by Turbett Surgical, Inc. Due to Pod may...
The Issue: Pod may have weld failures breaching the sterile barrier and result in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oncentra Brachy radiation therapy planning system software. Recalled by...
The Issue: A reconstruction error may occur when using the Catheter Bending...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SHIP KIT Recalled by Cardiac Assist, Inc Due to A software update (v1.1.5)...
The Issue: A software update (v1.1.5) has been developed to address the issue of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Denticator PICK-A-DENT Recalled by Young Dental Manufacturing I, LLC Due to...
The Issue: mislabeled product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgidac Uncoated Braided Polyester suture Product Description D-1764K...
The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sofsilk Coated Braided Silk Suture Product Description CS-211 SOFSILK* 4-0...
The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monofilament Nylon Suture (McKesson Branded) and Coated Braided Silk Suture...
The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dermalon Monofilament Nylon Suture: (1) 88861741-11 DERMALON* 6-0 BLU 45CM...
The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Suture Pack Product Description: US1638 CUSTOM SUTURE PACK US1756...
The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.