Safety Recalls

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17,567 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.

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Showing 6,201–6,250 of 17,567

Medical Device Recall · September 8, 2025
ICU Medical, Inc.
ICU Medical 21" Ext Set w/ChemoLock Port, Clamp, Graduated Connector REF: CL3360
Port weld of drug transfer device may separate or break during use and potentially result in a leak.
Class II
Medical Device Recall · September 6, 2025
Iantrek Inc.
Cyclopen Microinterventional Cyclodialysis System. Model Number: CP-300. Product Description: The CycloPen Microinterventional Cyclodialysis device is a manual surgical instrument used for the ab-i
Potential for compromised integrity of the sterile packaging.
Class II
Medical Device Recall · September 6, 2025
Iantrek Inc.
C-Rex UNO Microinterventional Goniotomy Instrument. Model Number: CRX-120. Product Description: The C-Rex UNO Microinterventional Goniotomy Instrument is a sterile single use disposable manual sur
Potential for compromised integrity of the sterile packaging.
Class II
Food Recall · September 5, 2025
CHETAK NEW YORK LLC
Deep-brand Select Bhindi Cut Okra KEEP FROZEN a) Net Wt. 12 oz (340 g); b) Net Wt. 1 LB 8 oz. (24 oz.) (680 g); c) Net Wt. 2 LB (907 g)
Product tested positive Salmonella .
Class I
Food Recall · September 5, 2025
CHETAK NEW YORK LLC
Deep-brand Premium Select Baby Bhindi KEEP FROZEN Net Wt. 12 oz (340 g)
Product tested positive Salmonella .
Class I
Medical Device Recall · September 5, 2025
Philips Ultrasound, Inc
Philips X3-1 Ultrasound Transducer
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Class III
Medical Device Recall · September 5, 2025
Philips Ultrasound, Inc
Philips OMNI II TEE Ultrasound Transducer
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Class III
Medical Device Recall · September 5, 2025
Spacelabs Healthcare, Inc.
Brand Name: Branding is not applied to this product. Product Name: DVI display cables Model/Catalog Number: 012-0893-01 Software Version: N/A Product Description: 16 inch DVI-I to DVI-I male/male
Due to display cables used for monitors were not in compliance with electromagnetic interference from inadequately shielded cables which may pose serious risk to patient's safety by interfering with the operation of another electronically sensitive medical device are in use.
Class II
Food Recall · September 5, 2025
CHETAK NEW YORK LLC
Deep-brand PREMIUM Select Sweet Corn KEEP FROZEN Net Wt. 2 LB (907 g)
Product tested positive Salmonella .
Class I
Medical Device Recall · September 5, 2025
Philips Ultrasound, Inc
Philips C9-4 Ultrasound Transducer
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Class III
Food Recall · September 5, 2025
CHETAK NEW YORK LLC
Deep-brand Indian Kitchen Quick Cubes READY FOR COOKING Garlic of India KEEP FROZEN Net Wt. 10 oz. (283 g)
Product tested positive Salmonella .
Class I
Food Recall · September 5, 2025
CHETAK NEW YORK LLC
Deep-brand Select Tindora Net Wt. 12 oz. (340 g) KEEP FROZEN
Product tested positive Salmonella .
Class I
Food Recall · September 5, 2025
CHETAK NEW YORK LLC
Deep-brand PREMIUM Select Hot Green Chillies Net Wt. 12 oz. (340 g) KEEP FROZEN
Product tested positive Salmonella .
Class I
Food Recall · September 5, 2025
CHETAK NEW YORK LLC
Deep-brand PREMIUM Select Aviyal Mix KEEP FROZEN Net Wt. 14.1 oz. (400 g)
Product tested positive Salmonella .
Class I
Food Recall · September 5, 2025
CHETAK NEW YORK LLC
Deep-brand PREMIUM Select Diced Green Mango KEEP FROZEN Net Wt. 12 oz. (340 g)
Product tested positive Salmonella .
Class I
Food Recall · September 5, 2025
CHETAK NEW YORK LLC
Deep-brand PREMIUM Select Fansi Cut French Beans Net Wt. 12 oz. (340 g) KEEP FROZEN
Product tested positive Salmonella .
Class I
Food Recall · September 5, 2025
CHETAK NEW YORK LLC
Deep-brand Premium Select Methi Blocks KEEP FROZEN Net Wt. 12 oz. (340 g)
Product tested positive Salmonella .
Class I
Food Recall · September 5, 2025
CHETAK NEW YORK LLC
Deep-brand Premium Select Punjabi Tinda KEEP FROZEN Net Wt. 12 oz. (340 g)
Product tested positive Salmonella .
Class I
Medical Device Recall · September 5, 2025
Spacelabs Healthcare, Inc.
Brand Name: Branding is not applied to this product. Product Name: DVI display cables Model/Catalog Number: 012-0895-12 Software Version: N/A Product Description: 12 foot DVI-I to DVI-I male/male
Due to display cables used for monitors were not in compliance with electromagnetic interference from inadequately shielded cables which may pose serious risk to patient's safety by interfering with the operation of another electronically sensitive medical device are in use.
Class II
Food Recall · September 5, 2025
CHETAK NEW YORK LLC
Deep-brand PREMIUM Select Red Guava Slices KEEP FROZEN Net Wt. 12 oz. (340 g)
Product tested positive Salmonella .
Class I
Food Recall · September 5, 2025
CHETAK NEW YORK LLC
Deep-brand PREMIUM Select Dudhi (Lauki) Diced Bottle Gourd KEEP FROZEN Net Wt. 12 oz. (340 g)
Product tested positive Salmonella .
Class I
Medical Device Recall · September 5, 2025
Philips Ultrasound, Inc
Philips L12-5 Ultrasound Transducer
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Class III
Food Recall · September 5, 2025
CHETAK NEW YORK LLC
Deep-brand PREMIUM Select Garlic Cloves Net Wt. 12 oz. (340 g) KEEP FROZEN
Product tested positive Salmonella .
Class I
Food Recall · September 5, 2025
CHETAK NEW YORK LLC
Deep-brand Premium Select Surti Papdi Lilva Net Wt. 12 oz. (340g) KEEP FROZEN
Product tested positive Salmonella .
Class I
Drug Recall · September 5, 2025
Sandoz Inc
Cyclophosphamide Injection 500 mg/5 mL (100 mg/mL), Hazardous Drug, Rx Only, Sterile, 5mL Multiple Dose Vial, Manufactured in Austria by Fareva Unterach GmbH for Sandoz Inc., Princeton, NJ 08540, Prod
cGMP deviations: Temperature excursion during transportation.
Class II
Vehicle Recall · September 5, 2025
Ford Motor Company
2025 FORD F-250 SD, 2025 FORD F-350 SD
A fuel leak in the presence of an ignition source such as hot engine components, can increase the risk of a fire.
Unclassified
Medical Device Recall · September 5, 2025
Philips Ultrasound, Inc
Philips L17-5 Ultrasound Transducer
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Class III
Drug Recall · September 5, 2025
Apotex Corp.
Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution, 0.2%/0.5%, a) 5 mL and b) 10 mL, Rx Only, Sterile, Manufactured by: Apotex Inc., Richmond Hill, Ontario, Canada, L4C 5H2, Manufactured for: Ap
Lack of Assurance of Sterility; atypical weight loss due to improper bottle sealing leading to potential sterility concerns
Class II
Vehicle Recall · September 5, 2025
Honda (American Honda Motor Co.)
2025 ACURA RDX
A loss of power steering assist can require greater steering effort, increasing the risk of a crash or injury.
Unclassified
Food Recall · September 5, 2025
CHETAK NEW YORK LLC
Deep-brand PREMIUM Select Amla KEEP FROZEN Net Wt. 12 oz. (340 g)
Product tested positive Salmonella .
Class I
Food Recall · September 5, 2025
CHETAK NEW YORK LLC
Deep-brand PREMIUM Select Turmeric Yellow Haldi KEEP FROZEN Net Wt. 12 oz. (340 g)
Product tested positive Salmonella .
Class I
Food Recall · September 5, 2025
CHETAK NEW YORK LLC
Deep-brand Select Tindora Net Wt. 1 LB 8 oz. (24 oz.) (680 g) KEEP FROZEN
Product tested positive Salmonella .
Class I
Food Recall · September 5, 2025
CHETAK NEW YORK LLC
Deep-brand PREMIUM Select Green Peas KEEP FROZEN a) Net Wt. 3.85 LB. (1.75 kg); b) Net Wt. 2 LB. (907 g)
Product tested positive Salmonella .
Class I
Medical Device Recall · September 5, 2025
GE Medical Systems, SCS
AW Server 2.0, AW Server 3.0, AW Server 3.1, AW Server 3.2
Firm has identified a security vulnerability in AW Server products. If exploited, a malicious actor could compromise the confidentiality, integrity, and availability of patient data.
Class II
Vehicle Recall · September 5, 2025
Honda (American Honda Motor Co.)
2025 HONDA CRF1100
The inability to use the horn or switch the headlight from low beam to high beam can increase the risk of a crash or injury.
Unclassified
Medical Device Recall · September 5, 2025
Wipro GE Healthcare Private Ltd.
GE Healthcare Carescape Central Station (CSCS) V3 MAS800 Desktop with software version V3.0.5; Part Number 5867474-04; Medical Display, cathode ray tube
Carescape Central Station (CSCS), software version V3.0.5, can cause the system to enter a continuous reboot cycle. If this occurs, a loss of central monitoring of connected patients could result. This issue occurs only when the number of central stations connected to the network is 118, 119 or 120.
Class II
Food Recall · September 5, 2025
CHETAK NEW YORK LLC
Deep-brand Premium Select Kantola KEEP FROZEN Net Wt. 12 oz. (340 g)
Product tested positive Salmonella .
Class I
Food Recall · September 5, 2025
CHETAK NEW YORK LLC
Deep-brand Select Val Papdi Net Wt. 12 oz. (340 g) KEEP FROZEN
Product tested positive Salmonella .
Class I
Food Recall · September 5, 2025
CHETAK NEW YORK LLC
Deep-brand PREMIUM Select Dum Aloo (Cooked) Net Wt. 12 oz. (340 g) KEEP FROZEN
Product tested positive Salmonella .
Class I
Food Recall · September 5, 2025
CHETAK NEW YORK LLC
Deep-brand PREMIUM Select Tuvar Lilva Net Wt. 12 oz. (340 g) KEEP FROZEN
Product tested positive Salmonella .
Class I
Medical Device Recall · September 5, 2025
Philips Ultrasound, Inc
Philips S5-2 Ultrasound Transducer
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Class III
Food Recall · September 5, 2025
CHETAK NEW YORK LLC
Deep-brand Ponk With Tangy Sev KEEP FROZEN Net Wt. 6 oz. (170 g)
Product tested positive Salmonella .
Class I
Food Recall · September 5, 2025
CHETAK NEW YORK LLC
Deep-brand Instant Stuffing For Pani Puri KEEP FROZEN Net Wt. 1 LB. (454 g)
Product tested positive Salmonella .
Class I
Medical Device Recall · September 5, 2025
Philips Ultrasound, Inc
Philips Mini Multi TEE Ultrasound Transducer
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Class III
Food Recall · September 5, 2025
CHETAK NEW YORK LLC
Deep-brand PREMIUM Select Peas and Carrots KEEP FROZEN Net Wt. 2 LB (907 g)
Product tested positive Salmonella .
Class I
Food Recall · September 5, 2025
CHETAK NEW YORK LLC
Deep-brand Premium Select Sambhar Mix KEEP FROZEN Net Wt. 12 oz. (340 g)
Product tested positive Salmonella .
Class I
Food Recall · September 5, 2025
CHETAK NEW YORK LLC
Deep-brand Premium Select Surti Undhiu Mix Net Wt. 12 oz. (340 g) KEEP FROZEN
Product tested positive Salmonella .
Class I
Food Recall · September 5, 2025
CHETAK NEW YORK LLC
Deep-brand PREMIUM Select Green Garlic KEEP FROZEN Net Wt. 12 oz. (340 g)
Product tested positive Salmonella .
Class I
Food Recall · September 5, 2025
CHETAK NEW YORK LLC
Deep-brand Premium Select Suran Net Wt. 12 oz. (340 g) KEEP FROZEN
Product tested positive Salmonella .
Class I
Medical Device Recall · September 5, 2025
MICROVENTION INC.
Flow Re-Direction Endoluminal Devices: FRED 27, REF: FRED5019, FRED5029, FRED4528, FRED4026, FRED5526, FRED4508, FRED5514, FRED3536, FRED3511, FRED5014, FRED3516, MV-F451827; FRED X 27, REF: XFRED401
Flow diverter may have a manufacturing issue related to the tantalum length and/or tantalum attachment pattern, which may lead the device to be incompletely open or not properly apposed to the vessel wall, which may necessitate device recapture and withdrawal of the delivery system and microcatheter together. Insufficient apposition could lead to long-term health consequences.
Class II