Safety Recalls

15,271 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.

Showing 7,651–7,700 of 15,271

• Food Recall · March 4, 2025

  Liaoning Cheng Da (USA) Inc

  Wangzhine branded Hot Pot Sauce (SPICY); Net Weight: 160 Grams, 5.64OZ; 36 units/case; UPC# 6907592001382

  (Imported) Hot Pot Sauce (SPICY) contains undeclared allergens (Wheat and Soy)

  Class I

• Medical Device Recall · March 4, 2025

  Abbott Diagnostics Scarborough, Inc.

  Brand Name: ID NOW RSV 24T Product Name: ID NOW RSV 24T Model/Catalog Number: 435-000 Software Version: N/A Product Description: Respiratory virus panel nucleic acid assay system Component: No

  the impacted lots have a higher occurrence of invalid rates when compared to the product Instructions for Use.

  Class II

• Food Recall · March 4, 2025

  Liaoning Cheng Da (USA) Inc

  Wangzhine branded Hot Pot Sauce; Net Weight: 160 Grams, 5.64OZ; 36 units/case; UPC# 6907592001375

  (Imported) Hot Pot Sauce contains undeclared allergens (Wheat and Soy)

  Class I

• Medical Device Recall · March 4, 2025

  Abbott Diagnostics Scarborough, Inc.

  Brand Name: ID NOW COVID-19 2.0 24T Product Name: ID NOW COVID-19 2.0 24T Model/Catalog Number: 192-000 Software Version: N/A Product Description: Simple Point-Of-Care Device To Detect Sar-Cov-2 Nucle

  the impacted lots have a higher occurrence of invalid rates when compared to the product Instructions for Use.

  Class II

• Medical Device Recall · March 4, 2025

  ZOLL Circulation, Inc.

  Brand Name: AutoPulse NXT Resuscitation System Product Name: AutoPulse NXT Platform Model/Catalog Number: Model 200 (Catalog Number: 8700-001070-1) Software Version: Version 2.0.1 Product Descript

  AutoPulse NXT Resuscitation System may not provide adequate chest compressions or may stop compressions due to code FC1060.

  Class I

• Medical Device Recall · March 3, 2025

  MEDLINE INDUSTRIES, LP - Northfield

  Medline Convenience kits used for various procedures: 1) INTUBATION TRAY, Model Number: MNS10395;

  There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

  Class II

• Medical Device Recall · March 3, 2025

  MEDLINE INDUSTRIES, LP - Northfield

  Medline Convenience kits used for various procedures: 1) HERNIA REPAIR TOTE, Model Number: DYNJ908337C

  There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

  Class II

• Medical Device Recall · March 3, 2025

  MEDLINE INDUSTRIES, LP - Northfield

  Medline Convenience kits used for various procedures: 1) RHINOPLASTY PACK, Model Number: DYNJ84116A

  There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

  Class II

• Medical Device Recall · March 3, 2025

  MEDLINE INDUSTRIES, LP - Northfield

  Medline Convenience kits used for various procedures: 1) DR. KHAN CABG ADDS PACK, Model Number: DYNJ59310D; 2) CARDIAC STERNAL PACK, Model Number: DYNJ32436A; 3) VEIN CLOSURE PACK, Model Number:

  There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

  Class II

• Medical Device Recall · March 3, 2025

  MEDLINE INDUSTRIES, LP - Northfield

  Medline Convenience kits used for various procedures: 1) SKIN LESION SET, Model Number: MNS6270

  There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

  Class II

• Medical Device Recall · March 3, 2025

  MEDLINE INDUSTRIES, LP - Northfield

  Medline Convenience kits used for various procedures: 1) PERI GYN PACK, Model Number: DYNJ80786; 2) D & C HYSTEROSCOPY PACK, Model Number: DYNJ21937J; 3) VAGINAL HYSTERECTOMY WRH-LF, Model Number

  There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

  Class II

• Medical Device Recall · March 3, 2025

  MEDLINE INDUSTRIES, LP - Northfield

  Medline Convenience kits used for various procedures: 1) IV PACK SOUTH, Model Number: DYNJ88422

  There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

  Class II

• Medical Device Recall · March 3, 2025

  ZIMMER ORTHOPEDICS MANFACTURING LIMITED-GALWAY

  Comprehensive Shoulder Stem, Comprehensive Micro Stem, Comprehensive Mini Stem; uncemented shoulder prosthesis, Model Nos. 113605, 113606, 113607, 113627

  Five complaints received where surgeon was unable to remove and/or connect the inserter with the stem during surgery due to excess material remaining within the taper. Issue may lead to clinically significant extension of surgery to find a replacement.

  Class II

• Medical Device Recall · March 3, 2025

  MEDLINE INDUSTRIES, LP - Northfield

  Medline Convenience kits used for various procedures: 1) MINOR BASIN -SMH, Model Number: DYNJ907733B

  There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

  Class II

• Medical Device Recall · March 3, 2025

  MEDLINE INDUSTRIES, LP - Northfield

  Medline Convenience kits used for various procedures: 1) LABOR AND DELIVERY PACK-LF, Model Number: DYNJ26971L; 2) VAGINAL DELIVERY PACK-LF, Model Number: DYNJ0378319P; 3) VUWC OB PACK, Model Numb

  There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

  Class II

• Medical Device Recall · March 3, 2025

  Tornier, Inc

  stryker Latitude EV HUMERAL REVISION STEM TRIAL, L: 150mm, Size: LARGE, Side: RIGHT, REF 9030103; Prosthesis, Elbow, Semi-Constrained, Cemented

  A specific lot of Latitude Humeral Trial Stems has the incorrect direct part marking. " Laser Marked: 9030103, Humeral Stem Trial 150mm Large / Right, Yellow color indicator (incorrect) " Device Actually: 9030092, Humeral Stem Trial 150mm Medium / Left, Red color indicator (correct)

  Class II

• Medical Device Recall · March 3, 2025

  MEDLINE INDUSTRIES, LP - Northfield

  Medline Convenience kits used for various procedures: 1) ANGIOGRAPHY DRAPE PACK, Model Number: HCP075G; 2) ENSEMBLE CORONAROGRAPHIE-LF, Model Number: DYNJ64354A; 3) RADIOL ANGIO PACK-LF, Model Nu

  There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

  Class II

• Medical Device Recall · March 3, 2025

  MEDLINE INDUSTRIES, LP - Northfield

  Medline Convenience kits used for various procedures: 1) RHINOPLASTY PACK, Model Number: DYNJ27333F

  There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

  Class II

• Medical Device Recall · March 3, 2025

  MEDLINE INDUSTRIES, LP - Northfield

  Medline Convenience kits used for various procedures: 1) UTHET TYLER OB PACK, Model Number: DYNJ68673; 2) D AND C PACK, Model Number: DYNJ66290A; 3) D & C PACK-LF, Model Number: DYNJ24159C; 4)

  There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

  Class II

• Medical Device Recall · March 3, 2025

  MEDLINE INDUSTRIES, LP - Northfield

  Medline Convenience kits used for various procedures: 1) LARGE BIOPSY PACK NTX, Model Number: DYNJ68393A; 2) SOFT TISSUE BIOPSY PACK, Model Number: DYNJ81441B; 3) BILAT TESTICULAR SPERM EXTRACT,

  There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

  Class II

• Medical Device Recall · March 3, 2025

  MEDLINE INDUSTRIES, LP - Northfield

  Medline Convenience kits used for various procedures: 1) CUSTOM BLOCK KEMP PACK-LF, Model Number: DYNJ0371999G;

  There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

  Class II

• Medical Device Recall · March 3, 2025

  MEDLINE INDUSTRIES, LP - Northfield

  Medline Convenience kits used for various procedures: 1) PAIN PACK, Model Number: DYNJ67577A; 2) PAIN TRIAL PACK, Model Number: DYNJ67576A;

  There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

  Class II

• Medical Device Recall · March 3, 2025

  MEDLINE INDUSTRIES, LP - Northfield

  Medline Convenience kits used for various procedures: 1) ED CRASH C-SECTION TRAY, Model Number: MNS13635A; 2) C-SECTION PCH-LF, Model Number: DYNJ81281; 3) C-SECTION PACK-LF, Model Number: OBK387

  There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

  Class II

• Medical Device Recall · March 3, 2025

  MEDLINE INDUSTRIES, LP - Northfield

  Medline Convenience kits used for various procedures: 1) ANGIO CONSOLIDATED PACK, Model Number: DYNJHTCAD1; 2) ANGIOGRAPHY TRAY-LF, Model Number: DYNJ05350V; 3) ANGIOGRAPHY PACK, Model Number: DY

  There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

  Class II

• Food Recall · March 3, 2025

  U.S. Tov, Inc. dba U.S. Trading Company

  DRIED LILY FLOWERS Net Weight 2.5 oz (70g) Ingredients: Lily flower (Hemerocallis citrina) Distributed by: U.S. TRADING COMPANY Hayward, CA 94545-1130 Product of China

  Undeclared sulfites

  Class III

• Medical Device Recall · March 3, 2025

  MEDLINE INDUSTRIES, LP - Northfield

  Medline Convenience kits used for various procedures: 1) LINE INSERTION PACK, Model Number: DYNJ44949C; 2) PICC LINE INSERTION BJC-LF, Model Number: DYNJ41682C; 3) SUPERFICIAL VENOUS PROCEDURE, M

  There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

  Class II

• Medical Device Recall · March 3, 2025

  MEDLINE INDUSTRIES, LP - Northfield

  Medline Convenience kits used for various procedures: 1) OCULOPLASTIC PICK PACK, Model Number: DYNJ43914B; 2) PLASTIC PACK, Model Number: DYNJ65109; 3) PLASTIC PROCEDURE PACK, Model Number: DYNJ3

  There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

  Class II

• Medical Device Recall · March 3, 2025

  MEDLINE INDUSTRIES, LP - Northfield

  Refer to RES

  There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

  Class II

• Medical Device Recall · March 3, 2025

  MEDLINE INDUSTRIES, LP - Northfield

  Medline Convenience kits used for various procedures: 1) NAIL PACK, Model Number: SUT15830A;

  There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

  Class II

• Medical Device Recall · March 3, 2025

  MEDLINE INDUSTRIES, LP - Northfield

  Medline Convenience kits used for various procedures: 1) BASIC CATARACT, Model Number: DYNJ41097A; 2) PK EYE, Model Number: DYNJ60631B; 3) CATARACT PACK, Model Number: DYNJ80316A; 4) BASIC EYE

  There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

  Class II

• Medical Device Recall · March 3, 2025

  MEDLINE INDUSTRIES, LP - Northfield

  Medline Convenience kits used for various procedures: 1) CW PERI GYN, Model Number: DYNJ80807B

  There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

  Class II

• Medical Device Recall · March 3, 2025

  MEDLINE INDUSTRIES, LP - Northfield

  Medline Convenience kits used for various procedures: 1) PRECIP TRAY, Model Number: MNS12590

  There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

  Class II

• Medical Device Recall · March 3, 2025

  MEDLINE INDUSTRIES, LP - Northfield

  Medline Convenience kits used for various procedures: 1) T&A ENDO PACK, Model Number: DYNJ59620A; 2) TRAY ADD A CATH FOL UM MF 10ML, Model Number: DYND150200S

  There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

  Class II

• Medical Device Recall · March 3, 2025

  MEDLINE INDUSTRIES, LP - Northfield

  Refer to RES

  There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

  Class II

• Medical Device Recall · March 3, 2025

  MEDLINE INDUSTRIES, LP - Northfield

  Medline Convenience kits used for various procedures: 1) DENTAL PACK-LF, Model Number: DYNJ84880; 2) DENTAL PACK, Model Number: DYNJ56229A; 3) DENTAL PACK-LF, Model Number: PHS807626F; 4) DENTA

  There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

  Class II

• Medical Device Recall · March 3, 2025

  MEDLINE INDUSTRIES, LP - Northfield

  Medline Convenience kits used for various procedures: 1) STANDARD D&C, Model Number: DYNJ69733; 2) NHS - LAP BOWEL GNG, Model Number: DYNJ39904A; 3) LAPAROSCOPY GYN SURGERY PA, Model Number: DYNJ

  There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

  Class II

• Medical Device Recall · March 3, 2025

  MEDLINE INDUSTRIES, LP - Northfield

  Medline Convenience kits used for various procedures: 1) NEURO PACK WRO-LF, Model Number: DYNJ41856C; 2) STIM IMPLANT PACK, Model Number: DYNJ53032C; 3) WMC VP SHUNT PACK-LF, Model Number: DYNJ50

  There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

  Class II

• Medical Device Recall · March 3, 2025

  MEDLINE INDUSTRIES, LP - Northfield

  Medline Convenience kits used for various procedures: 1) ARTHROSCOPIE DU GENOU-LF, Model Number: DYNJ40229A; 2) ARTHROSCOPY PACK-LF, Model Number: OPK382N; 3) ARTHROSCOPY NEW TEGH-LF, Model Numbe

  There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

  Class II

• Medical Device Recall · March 3, 2025

  Terumo Cardiovascular Systems Corporation

  Terumo CDI OneView Monitoring System Hematocrit / Oxygen Saturation Probe, Catalog Number REF CD1754

  During some clinical cases, it has been observed that the SO2 value may periodically appear as dashes on the Touchscreen Display indicating unavailable data. In these cases, a yellow low-limit alarm will also be triggered to the user, due to the dashed-out value.

  Class II

• Medical Device Recall · March 3, 2025

  MEDLINE INDUSTRIES, LP - Northfield

  Medline Convenience kits used for various procedures: 1) T A PACK, Model Number: DYNJ67791A; 2) NASAL PACK, Model Number: DYNJ66514; 3) ENT PACK, Model Number: DYNJ67775A; 4) T/A ENDO PACK, M

  There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

  Class II

• Medical Device Recall · March 3, 2025

  MEDLINE INDUSTRIES, LP - Northfield

  Medline Convenience kits used for various procedures: 1) CSTM PACEMAKER DRAPE PACK, Model Number: DYNJCD0339

  There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

  Class II

• Medical Device Recall · March 3, 2025

  Baxter Healthcare Corporation

  Baxter NovumIQ Syringe INFUSION SYSTEM , REF 40800BAXUS

  Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for the Novum IQ syringe pumps listed below due to an incorrectly installed gasket. A gasket failure could lead to potential fluid ingress due to cleaning, or as a result of an IV fluid spill.

  Class II

• Medical Device Recall · March 3, 2025

  MEDLINE INDUSTRIES, LP - Northfield

  Medline Convenience kits used for various procedures: 1) UNIVERSAL DRAPE PACK, Model Number: DYNJCD0239

  There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

  Class II

• Medical Device Recall · March 3, 2025

  MEDLINE INDUSTRIES, LP - Northfield

  Refer to RES

  There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

  Class II

• Drug Recall · February 28, 2025

  Glenmark Pharmaceuticals Inc., USA

  Carvedilol Tablets USP 6.25 mg, a.)100-count bottle (NDC 68462-163-01), b.) 500-count bottle (NDC 68462-163-05) Rx Only, Manufactured by: Glenmark Pharmaceuticals Ltd., Manufactured for: Glenmark Phar

  CGMP Deviations; presence 'N-Nitroso Carvedilol I' Impurity above the recommended acceptable intake limit

  Class II

• Medical Device Recall · February 28, 2025

  Stryker Spine

  Monterey AL Implant Inserter; 10/12mm; Catalog 48019100.

  Potential for the gold unlock button to separate from the inserter.

  Class II

• Food Recall · February 28, 2025

  LITTLE LEAF FARMS LLC

  Little Leaf Farms brand Southwest Salad Kit; 7.5 oz, clear plastic clamshell; UPC: 857394006220

  Product may contain incorrect salad dressing, resulting in fish and wheat being undeclared.

  Class I

• Drug Recall · February 28, 2025

  Glenmark Pharmaceuticals Inc., USA

  Carvedilol Tablets USP 25 mg, 500 -Count bottle, Rx Only, Manufactured by: Glenmark Pharmaceuticals Ltd., Manufactured for Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ 07430. NDC 68462-165-05.

  CGMP Deviations; presence 'N-Nitroso Carvedilol I' Impurity above the recommended acceptable intake limit

  Class II

• Medical Device Recall · February 28, 2025

  Philips Medical Systems Nederland B.V.

  Spectral CT on Rails, Software Version Number 5.1.0, Model number: 728334;

  Multiple problems identified with the software version leading to various scanning and image issues, and unintended device movement.

  Class II

• Drug Recall · February 28, 2025

  Glenmark Pharmaceuticals Inc., USA

  Carvedilol Tablets USP 3.125mg Tablets a.)100-count bottle (NDC 68462-162-01), b.) 500-count bottle (NDC 68462-162-05), Rx Only, Manufactured by: Glenmark Pharmaceuticals Ltd., Manufactured for: Gle

  CGMP Deviations; presence 'N-Nitroso Carvedilol I' Impurity above the recommended acceptable intake limit

  Class II