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. 2,469 recalls have been distributed to Indiana in the last 12 months.
Showing 41501–41520 of 53,528 recalls
Recalled Item: Talenti Gelato & Sorbetto Recalled by Unilever United States, Inc. Due to...
The Issue: Talenti Gelato & Sorbetto, a Unilever Company is voluntarily recalling a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Kinemax Stem Extenders Recalled by Stryker Howmedica Osteonics Corp. Due to...
The Issue: Stryker received four customer complaints reporting that inside the box...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxecta(TM) (oxycodone HCl) tablets Recalled by Pfizer Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxecta(TM) (oxycodone HCl) tablets Recalled by Pfizer Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ENDOPATH ECHELON" Vascular White Reload for Advanced Placement Tip Recalled...
The Issue: During an internal inspection of the production process the firm discovered...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ziploop Button Product Usage: The Ziploop Button is a non-resorbable...
The Issue: The firm is recalling ToggleLocs and Ziploops manufactured in May and July...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vitagel Recalled by Orthovita, Inc., dBA Stryker Orthobiologics. Due to...
The Issue: Several shipments of Vitagel product (a surgical hemostat) required to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ToggleLoc Recalled by Biomet, Inc. Due to The firm is recalling ToggleLocs...
The Issue: The firm is recalling ToggleLocs and Ziploops manufactured in May and July...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIS27T - Lacrimal Intubation Set RX Only Sterile Used in Recalled by Quest...
The Issue: Expiration date incorrectly printed in Manufacturing Date field on both...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Minivelle (estradiol transdermal system) 0.05 mg/day Recalled by Noven...
The Issue: Temperature Abuse: Prolonged exposure to temperatures outside of labeled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Colistimethate for Injection USP Recalled by Heritage Pharmaceuticals, Inc....
The Issue: Lack of Assurance of Sterility: Firm is recalling two injectable products...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: RIFAMPIN for Injection Recalled by Heritage Pharmaceuticals, Inc. Due to...
The Issue: Lack of Assurance of Sterility: Firm is recalling two injectable products...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amerigel Hydrogel Gauze Dressing 2 x 2 Recalled by Amerx Health Care Corp....
The Issue: Nonapproved labeling claims (Sterile)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Captiva's lumbar intervertebral fusion system Reamers (color code rings on...
The Issue: It is possible for the titanium color-coded ring to detach from the Reamers.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASSO NAV Duo Loop eco Catheters Recalled by Biosense Webster, Inc. Due to...
The Issue: Biosense Webster is recalling the LASSO NAV Duo Loop eco Catheters because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Droperidol injection Recalled by SCA Pharmaceuticals Due to Presence of...
The Issue: Presence of particulate.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Epi breads Recalled by Lavoi Corporation d/b/a/ Epi De France Due to...
The Issue: Undeclared allergen: Bread products were manufactured using raw material...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Epi breads Recalled by Lavoi Corporation d/b/a/ Epi De France Due to...
The Issue: Undeclared allergen: Bread products were manufactured using raw material...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Epi breads Recalled by Lavoi Corporation d/b/a/ Epi De France Due to...
The Issue: Undeclared allergen: Bread products were manufactured using raw material...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fire House Subs Recalled by Lavoi Corporation d/b/a/ Epi De France Due to...
The Issue: Undeclared allergen: Bread products were manufactured using raw material...
Recommended Action: Do not consume. Return to store for a refund or discard.