Product Recalls in Wyoming
Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,383 recalls have been distributed to Wyoming in the last 12 months.
Showing 24281–24300 of 27,462 recalls
Recalled Item: SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT PUNCH NONCEMENTED Size 1-1.5 HP Recalled...
The Issue: DePuy Orthopaedics, Inc. is issuing a voluntary device correction of the HP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT KEEL PUNCH CEMENTED Size 4-7 Recalled by...
The Issue: DePuy Orthopaedics, Inc. is issuing a voluntary device correction of the HP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT KEEL PUNCH NONCEMENTED Size 1-1.5 Recalled...
The Issue: DePuy Orthopaedics, Inc. is issuing a voluntary device correction of the HP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT PUNCH CEMENTED Size 1-1.5 HP Recalled by...
The Issue: DePuy Orthopaedics, Inc. is issuing a voluntary device correction of the HP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mega Needle Driver Recalled by Intuitive Surgical, Inc. Due to Firm has...
The Issue: Firm has become aware of the potential for detachment of the jaw insert for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Large Needle Driver Recalled by Intuitive Surgical, Inc. Due to Firm has...
The Issue: Firm has become aware of the potential for detachment of the jaw insert for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Innova IGS 630. Biplane Cardiovascular and Interventional...
The Issue: GE Healthcare has recently become aware of a potential safety issue with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HemosIL Low Abnormal Control 2 UNASSAYED Part Number: 0020003220 Recalled by...
The Issue: HemosIL Low, Abnormal, Normal Controls UNASSAYED (no-value assigned) lacks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens SOMATOM Definition Recalled by Siemens Medical Solutions USA, Inc...
The Issue: During clinical operation, a malfunction may occur causing a system display...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mobile X-ray System Recalled by Shimadzu Medical Systems Due to Shimadzu...
The Issue: Shimadzu Corporation is recalling the Shimadzu Mobile X-ray Sytems (MUX-100...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HemosIL Normal Control 1 UNASSAYED Part Number: 0020003120 Recalled by...
The Issue: HemosIL Low, Abnormal, Normal Controls UNASSAYED (no-value assigned) lacks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HemosIL High Abnormal Control 3 UNASSAYED Part Number: 0020003320 Recalled...
The Issue: HemosIL Low, Abnormal, Normal Controls UNASSAYED (no-value assigned) lacks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VerifyNow IIb/IIIa Test Recalled by Accumetrics Inc Due to Accumetrics is...
The Issue: Accumetrics is recalling the VerifyNow IIb/IIIa 10-Test because it contains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Renasys EZ PLUS Recalled by Smith & Nephew Inc. Due to Modification of the...
The Issue: Modification of the bacterial overflow guard (filter) and related changes to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Renasys EZ Recalled by Smith & Nephew Inc. Due to Modification of the...
The Issue: Modification of the bacterial overflow guard (filter) and related changes to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intubation Flexible Fiberscope Recalled by Karl Storz Endoscopy America Inc...
The Issue: KARL STORZ Endoscopy America, Inc. is recalling the Flexible Broncho...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RTC 25-C Inline Aerosol Tee Adapter. Intended to be used Recalled by...
The Issue: Some packages of the RTC 25-C may have been shipped to customers with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Broncho Flexible Fiberscope Recalled by Karl Storz Endoscopy America Inc Due...
The Issue: KARL STORZ Endoscopy America, Inc. is recalling the Flexible Broncho...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Trabecular Metal Total Ankle Talar Component Left Sizes 1-6 Recalled...
The Issue: As part of routine manufacturing process monitoring by Zimmer, it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sandel Healthcare Safety Devices Weighted Safety Scalpel 4# Disposable...
The Issue: Select lots of SANDEL Weighted Safety Scalpels are packaged with the scalpel...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.