Product Recalls in Indiana
Product recalls affecting Indiana — including food, drugs, consumer products, medical devices, and vehicles distributed to Indiana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,861 recalls have been distributed to Indiana in the last 12 months.
Showing 33201–33220 of 53,528 recalls
Recalled Item: NucliSENS magnetic extraction reagents Recalled by BioMerieux SA Due to A...
The Issue: A drift of the performance with the BK test (BK virus, worst case...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MagSIL (NucliSENS easyMAG Magnetic Silica) Recalled by BioMerieux SA Due to...
The Issue: A drift of the performance with the BK test (BK virus, worst case...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straumann Drill 1 Recalled by Straumann Manufacturing, Inc. Due to Drills...
The Issue: Drills cannot be inserted into handpiece due to tolerance specification not met
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straumann Twist Drill PRO ¿4.2mm Recalled by Straumann Manufacturing, Inc....
The Issue: Drills cannot be inserted into handpiece due to tolerance specification not met
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROTONIX I.V. (pantoprazole sodium) for Injection Recalled by Pfizer Inc....
The Issue: Subpotent Drug: Out of Specification (OOS) for potency at the 6-month...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Toms of Maine Naturally Dry Natural Powder Antiperspirant Stick Recalled by...
The Issue: Labeling: Label Mix Up- Incorrect back label applied to the product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Plush Puffs Marshmallows Toasty Coconut 4oz. and 2lb bulk bag Recalled by To...
The Issue: Undeclared allergen of milk from the declared ingredient coconut cream powder.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Durex Pleasure Pack . 3 ultra fine lubricated latex condoms Recalled by...
The Issue: Reckitt Benckiser LLC is recalling Durex Condoms Pleasure Packs due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Scope Power Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Siemens is providing a new installation of the Residual Current Monitor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS IMMULITE 2000/2000 Xpi Systems Intact PTH (Parathyroid Hormone) Test...
The Issue: Siemens is conducting this recall for the IMMULITE¿ 2000/IMMULITE¿ 2000 XPi...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G3 Opticage Expandable Interbody Fusion Device Recalled by Interventional...
The Issue: During implantation, the proximal end of the device could separate if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Perspective Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Siemens is providing a new installation of the Residual Current Monitor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Scope Recalled by Siemens Medical Solutions USA, Inc Due to Siemens...
The Issue: Siemens is providing a new installation of the Residual Current Monitor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K-Wire 1.4mm x 12in Non-Threaded Recalled by Amendia, Inc Due to The rods...
The Issue: The rods are packaged in packages with unacceptable seals. In some cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Black Widow 6.6mm x 20mm Screw Recalled by Amendia, Inc Due to There is a...
The Issue: There is a problem with the mating feature between the plate and screw which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dual Stylet Needle Recalled by Amendia, Inc Due to The rods are packaged in...
The Issue: The rods are packaged in packages with unacceptable seals. In some cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Savannah-T Straight Rod Recalled by Amendia, Inc Due to The rods are...
The Issue: The rods are packaged in packages with unacceptable seals. In some cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH Recalled by Teleflex Medical Due to Labeling Inconsistency: The...
The Issue: Labeling Inconsistency: The products have been labeled with the incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Black Widow Plate 19mm Plate Recalled by Amendia, Inc Due to There is a...
The Issue: There is a problem with the mating feature between the plate and screw which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mallinckrodt Pharmaceuticals INOmax DSIR Plus delivery system. Model 10007....
The Issue: Mallinckrodt discovered that some devices may have been manufactured with an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.