Product Recalls in Mississippi
Product recalls affecting Mississippi — including food, drugs, consumer products, medical devices, and vehicles distributed to Mississippi. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,429 recalls have been distributed to Mississippi in the last 12 months.
Showing 35481–35500 of 49,744 recalls
Recalled Item: DGDE Recalled by Implant Direct Sybron Manufacturing, LLC Due to Implant...
The Issue: Implant Direct Sybron Manufacturing, LLC is recalling 26 lots of DGDE...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model 5001102 MPS Delivery Set w/ arrest agent and additive cassettes...
The Issue: The products have been found to intermittently exhibit a seal failure during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProTrack Microcatheter. Model/Catalog Numbers CIC38-145 Recalled by Baylis...
The Issue: Microcatheter may have circumferential defects (cracks) along its shaft.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Auvi-Q (epinephrine injection Recalled by Sanofi-Aventis U.S. LLC Due to...
The Issue: Defective Delivery System; potential to have inaccurate dosage delivery
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Auvi-Q (epinephrine injection Recalled by Sanofi-Aventis U.S. LLC Due to...
The Issue: Defective Delivery System; potential to have inaccurate dosage delivery
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GRx HiCort 25 (hydrocortisone acetate 25 mg) Suppositories Recalled by...
The Issue: Marketed without an Approved NDA/ANDA: FDA has determined that the products...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carbo-O-Philic 40 Cream 40% (Urea) tubes Recalled by Geritrex Corp Due to...
The Issue: Marketed without an Approved NDA/ANDA: FDA has determined that the products...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Polyethylene Glycol 3350-GRX Powder 100% jars a) 8.4 oz (250 Recalled by...
The Issue: Marketed without an Approved NDA/ANDA: FDA has determined that the products...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carbo-O-Philic 40 Gel 40% (Urea) NET WT tube Recalled by Geritrex Corp Due...
The Issue: Marketed without an Approved NDA/ANDA: FDA has determined that the products...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Herr's Sour Cream & Onion Flavored Potato Chips Recalled by Herrs Foods Inc...
The Issue: Herr Foods Inc. has initiated a voluntary recall of certain bags of its...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: IOL Master 5.5: Software versions 7.5 and 7.7 Recalled by Carl Zeiss Meditec...
The Issue: IOL Master software versions 7.5 and 7.7 calculation printouts and exported...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IOL Master 500: Software versions 7.5 and 7.7 Recalled by Carl Zeiss Meditec...
The Issue: IOL Master software versions 7.5 and 7.7 calculation printouts and exported...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROLARYN Injectable Implant 1.0 cc Gel Recalled by Merz North America, Inc....
The Issue: The expiration date encoded in the UDI barcode on the label on the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cavity 8 Gauge Spine Wand indicated for resection Recalled by ArthroCare...
The Issue: There is cracking in the tray when the device is snapped into place. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROLARYN PLUS Injectable Implant 1.0 cc Plus Calcium Hydroxlyapatite (CaHA)...
The Issue: The expiration date encoded in the UDI barcode on the label on the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radiesse (+) Lidocaine Injectable Implant 1.5cc Recalled by Merz North...
The Issue: The expiration date encoded in the UDI barcode on the label on the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Meclizine Hydrochloride Tablets USP Recalled by Par Pharmaceutical Inc. Due...
The Issue: Failed Impurities/Degradation Specifications: Out of specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Meclizine Hydrochloride Tablets Recalled by Par Pharmaceutical Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications: Out of specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mountain Mix 2oz bag Recalled by Kanan Enterprises, Inc. Due to Undeclared Milk
The Issue: The firm was notified that the product contains undeclared Milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: David Trail Mix Sweet & Salty individual plastic bags net Recalled by...
The Issue: Product contains undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.